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Legislative Progress
Introduced
February 2, 2012
Latest Action
February 2, 2012
Primary Sponsor
Edward J. MarkeyDemocratic(MA)
Momentum (last 30 days)
0
score
0 actions · 0 new cosponsors · 0 votes
Speed vs cohort
0pct
0d open
vs 6,662 other HR bills in the 112th — cohort avg 39d
No CRS summary is available for this bill yet. The source title, actions, sponsors, and text versions below come from Congress.gov.
These links require the bill number to appear in the filing's source-reported specific issue text. Client expenses and lobbying-firm income are separate disclosure fields.
Filing registrants (6)
2012 · fourth_quarter · Medical/Disease Research/Clinical Labs
Bills with similar content found using semantic analysis.
Sources: Congress.gov
H.R. 1897 Alzheimer's Breakthrough Act of 2011, All sections H.R. 610 Making Investments Now for Dementia Act of 2011, All sections H.R. 3497 Modernizing our Drug & Diagnostics Evaluation and Regulator Network Cures Act", All sections S. 2113 Transforming the Regulatory Environment to Accelerate Access to Treatments Act, All sections H.Res 351/S.Res 176 Supporting a Semipostal Stamp to Support Medical Research Relating to Alzheimer's Disease, All sections. S.Res .434 / H. Res. 120 A resolution supporting the goal of preventing and effectively treating Alzheimer's disease by the year 2025, as articulated in the draft National Plan to Address Alzheimer's Disease from the Department of Health and Human Services, All sections. S.2069/H.R.3891 Spending Reductions through Innovations in Therapies Agenda Act of 2012, All sections S.2236 Advancing Breakthrough Therapies for Patients Act of 2012, All sections S.3187 Food and Drug Administration Safety and Innovation Act / H.R.5651 Food and Drug Administration Reform Act of 2012, All sections
Client expense: $150,000 · Firm income: Not reported
Government targets: Centers For Medicare and Medicaid Services (CMS), Food & Drug Administration (FDA), HOUSE OF REPRESENTATIVES, Health & Human Services, Dept of (HHS), Natl Institutes of Health (NIH), SENATE, Veterans Affairs, Dept of (VA)
2012 · fourth_quarter · Health Issues
Support the speedy implementation of the National Alzheimer's Project Act (NAPA) by HHS, and support Leaders Engaged on Alzheimer's Disease (LEAD) recommendations as to how to proceed. Support repeal of Section 6001 of the PPACA and remove all restrictions on physician-owned hospitals. (Support H.R. 1159 and H.R. 1186) Support extensive clinical trials, manufacturing inspections and post-market surveillance for all biosimilar drugs. Support higher PDUFA fees for biosimilar drugs to pay for the additional safeguards needed. Oppose federal budget cuts that would increase co-payments for home health care services under Medicare and/or Medicaid. Support all legislative and regulatory action to modernize the FDA and to speed new cures and therapies to patients. Support the Preservation of Access to Osteoporosis Testing for Medicare Beneficiaries Act of 2011 (S. 1096, H.R. 2020) Support Leaders Engaged on Alzheimer's Disease (LEAD) FY 2012 funding proposals in the amount of for $35 billion for the National Institutes of Health (NIH), $1.4 billion for the National Institute on Aging (NIA), $100 million for the Cures Acceleration Network (CAN), $11.46 million for the Alzheimer's Disease Supportive Services Program (ADSSP), $192 million for the National Family Caregiver Support Program (NFCSP), $50 million for the Lifespan Respite Care Program (LRCP), and$2.744 billion for the Food and Drug Administration (FDA), as well as $2 million for the Missing Alzheimer's Disease Patient Alert Program and $750,000 to organize and host a high-level meeting to focus on the global Alzheimer's disease crisis. Oppose proposals that would reduce Medicare payments for providers of drugs and biologics under Medicare Part B. Support the proposed Prescription Drug User Fee Act Reauthorization Agreement (PDUFA-V) now under consideration by the Congress for reauthorization. Support an extension of the Therapeutic Discovery Project Tax Credit (I.R.C. 48D). Oppose the proposed merger between pharmacy benefit managers (PBM) Medco Health Solutions (Medco) and Express Scripts, Inc. (ESI), including comments to the Federal Trade Commission on the merger's obvious danger to older Americans. Support the development of clearly-defined, comprehensive, patient-centric Essential Health Benefits rules under the Affordable Care Act. Support the Counterfeit Drug Penalty Enhancement Act of 2011. Joined other patient advocate organizations to urge the National Government Services to reconsider its policy regarding blanket denials under the Current Procedural Terminology (CPT) health and behavioral assessment and intervention codes (96150-96155) which restrict those medically appropriate services to Medicare beneficiaries with Alzheimer's disease. Joined other patient advocate organizations January 2012 to urge HHS to ensure that ACA "Essential Health Benefits" guidelines provide comprehensive, quality and affordable health care. This was in response to the HHS December 16, 2011 bulletin on Essential Health Benefits because the HHS bulletin did not provide adequate patient protections as intended under the ACA. Joined other patient advocate groups to support the Spending Reductions through Innovations in Therapies (SPRINT) Act (H.R. 3891 and S. 2064) Support H.R.5998, the USPSTF Transparency and Accountability Act of 2012. Support the creation of the National Center for AdvancingTranslations Sciences' (NCATS) "Discovering New Therapeutic Uses for Existing Molecules Initiative." Support the new Centers for Disease Control recommendations regarding the identification of chronic Hepatitis C infections. Urge all providers and payers to follow those same CDC recommendations. Oppose the substitution and use of unapproved and off-label drugs to treat age-related macular degeneration (AMD). Urge the Department of HHS to adopt the Advisory Council on Alzheimer's Research recommendations and ensure that the final National Alzheimer's Plan includes measures: Providing high-level, overall accountability for National Plan implementation. Recognizing and proposing a path forward to secure the public and private resources needed to achieve all of the goals. Forming robust public-private partnerships between government and industry to inform the research agenda, shorten the time and cost of developing therapies, and accelerate delivery of safe and effective treatments to individuals with Alzheimers. Fostering greater collaboration on research and other issues with international counterparts to achieve global coordination and progress toward a Global Alzheimers Action Plan. Expanding attention on early detection and diagnosis of Alzheimers disease. Ensuring access to the full array of long-term support services for special and emerging populations of people with Alzheimers disease, including younger people and those with developmental disabilities. Addressing caregivers physical and behavioral health. Expanding access to high quality, cost-effective and evidence based care and redoubling efforts to test and validate innovative care interventions. Support extensive clinical trials, manufacturing inspections and post-market surveillance for all biosimilar drugs. Support higher PDUFA fees for biosimilar drugs to pay for the additional safeguards needed. Support stiff restrictions on biosimilar "flexibility" (intentionally introducing differences to the molecule or the finished product) that adds high risk. Support distinctive labeling for safety, and install a strong track and trace system before the first biosimilar is allowed on the market. Support Congressional review and oversight to examine the National Alzheimer's Plan implementation progress. Support "unique naming" requirements for all biologic drugs, especially biosimilar drugs, as a matter of patient safety. Support full Medicare funding for dual energy x-ray absorptiometry (DXA) test reimbursement to fight osteoporosis. Support new extended funding (as under the expired Medicare Improvements for Patients and Providers Act or MIPPA) for Medicare low-income outreach and enrollment activities. Support the Medicare Part D prescription drug benefit program and the needed improvements to correct its limitations; including gaps in coverage, onerous cost-shifting created by specialty tiers, and restrictive utilization management tools. Robust formularies, coverage of the six protected drug classes, strong oversight, and transparency for consumers are also critical, as is a process for notice of non-coverage, and an appeals and exceptions process that is patient and provider friendly. Support all measures making Alzheimer's disease a continued top priority at the U.S. Food and Drug Administration (FDA).
Client expense: $42,249 · Firm income: Not reported
Government targets: Centers For Medicare and Medicaid Services (CMS), Federal Trade Commission (FTC), Food & Drug Administration (FDA), HOUSE OF REPRESENTATIVES, Health & Human Services, Dept of (HHS), SENATE
2012 · fourth_quarter · Health Issues
Support the speedy implementation of the National Alzheimer's Project Act (NAPA) by HHS, and support Leaders Engaged on Alzheimer's Disease (LEAD) recommendations as to how to proceed. Support repeal of Section 6001 of the PPACA and remove all restrictions on physician-owned hospitals. (Support H.R. 1159 and H.R. 1186) Support extensive clinical trials, manufacturing inspections and post-market surveillance for all biosimilar drugs. Support higher PDUFA fees for biosimilar drugs to pay for the additional safeguards needed. Oppose federal budget cuts that would increase co-payments for home health care services under Medicare and/or Medicaid. Support all legislative and regulatory action to modernize the FDA and to speed new cures and therapies to patients. Support the Preservation of Access to Osteoporosis Testing for Medicare Beneficiaries Act of 2011 (S. 1096, H.R. 2020) Support Leaders Engaged on Alzheimer's Disease (LEAD) FY 2012 funding proposals in the amount of for $35 billion for the National Institutes of Health (NIH), $1.4 billion for the National Institute on Aging (NIA), $100 million for the Cures Acceleration Network (CAN), $11.46 million for the Alzheimer's Disease Supportive Services Program (ADSSP), $192 million for the National Family Caregiver Support Program (NFCSP), $50 million for the Lifespan Respite Care Program (LRCP), and$2.744 billion for the Food and Drug Administration (FDA), as well as $2 million for the Missing Alzheimer's Disease Patient Alert Program and $750,000 to organize and host a high-level meeting to focus on the global Alzheimer's disease crisis. Oppose proposals that would reduce Medicare payments for providers of drugs and biologics under Medicare Part B. Support the proposed Prescription Drug User Fee Act Reauthorization Agreement (PDUFA-V) now under consideration by the Congress for reauthorization. Support an extension of the Therapeutic Discovery Project Tax Credit (I.R.C. 48D). Oppose the proposed merger between pharmacy benefit managers (PBM) Medco Health Solutions (Medco) and Express Scripts, Inc. (ESI), including comments to the Federal Trade Commission on the merger's obvious danger to older Americans. Support the development of clearly-defined, comprehensive, patient-centric Essential Health Benefits rules under the Affordable Care Act. Support the Counterfeit Drug Penalty Enhancement Act of 2011. Joined other patient advocate organizations to urge the National Government Services to reconsider its policy regarding blanket denials under the Current Procedural Terminology (CPT) health and behavioral assessment and intervention codes (96150-96155) which restrict those medically appropriate services to Medicare beneficiaries with Alzheimer's disease. Joined other patient advocate organizations January 2012 to urge HHS to ensure that ACA "Essential Health Benefits" guidelines provide comprehensive, quality and affordable health care. This was in response to the HHS December 16, 2011 bulletin on Essential Health Benefits because the HHS bulletin did not provide adequate patient protections as intended under the ACA. Joined other patient advocate groups to support the Spending Reductions through Innovations in Therapies (SPRINT) Act (H.R. 3891 and S. 2064) Support H.R.5998, the USPSTF Transparency and Accountability Act of 2012. Support the creation of the National Center for AdvancingTranslations Sciences' (NCATS) "Discovering New Therapeutic Uses for Existing Molecules Initiative." Support the new Centers for Disease Control recommendations regarding the identification of chronic Hepatitis C infections. Urge all providers and payers to follow those same CDC recommendations. Oppose the substitution and use of unapproved and off-label drugs to treat age-related macular degeneration (AMD). Urge the Department of HHS to adopt the Advisory Council on Alzheimer's Research recommendations and ensure that the final National Alzheimer's Plan includes measures: Providing high-level, overall accountability for National Plan implementation. Recognizing and proposing a path forward to secure the public and private resources needed to achieve all of the goals. Forming robust public-private partnerships between government and industry to inform the research agenda, shorten the time and cost of developing therapies, and accelerate delivery of safe and effective treatments to individuals with Alzheimers. Fostering greater collaboration on research and other issues with international counterparts to achieve global coordination and progress toward a Global Alzheimers Action Plan. Expanding attention on early detection and diagnosis of Alzheimers disease. Ensuring access to the full array of long-term support services for special and emerging populations of people with Alzheimers disease, including younger people and those with developmental disabilities. Addressing caregivers physical and behavioral health. Expanding access to high quality, cost-effective and evidence based care and redoubling efforts to test and validate innovative care interventions. Support extensive clinical trials, manufacturing inspections and post-market surveillance for all biosimilar drugs. Support higher PDUFA fees for biosimilar drugs to pay for the additional safeguards needed. Support stiff restrictions on biosimilar "flexibility" (intentionally introducing differences to the molecule or the finished product) that adds high risk. Support distinctive labeling for safety, and install a strong track and trace system before the first biosimilar is allowed on the market. Support Congressional review and oversight to examine the National Alzheimer's Plan implementation progress. Support "unique naming" requirements for all biologic drugs, especially biosimilar drugs, as a matter of patient safety. Support full Medicare funding for dual energy x-ray absorptiometry (DXA) test reimbursement to fight osteoporosis. Support new extended funding (as under the expired Medicare Improvements for Patients and Providers Act or MIPPA) for Medicare low-income outreach and enrollment activities. Support the Medicare Part D prescription drug benefit program and the needed improvements to correct its limitations; including gaps in coverage, onerous cost-shifting created by specialty tiers, and restrictive utilization management tools. Robust formularies, coverage of the six protected drug classes, strong oversight, and transparency for consumers are also critical, as is a process for notice of non-coverage, and an appeals and exceptions process that is patient and provider friendly. Support all measures making Alzheimer's disease a continued top priority at the U.S. Food and Drug Administration (FDA).
Client expense: Not reported · Firm income: $6,710
Government targets: Centers For Medicare and Medicaid Services (CMS), Federal Trade Commission (FTC), Food & Drug Administration (FDA), HOUSE OF REPRESENTATIVES, Health & Human Services, Dept of (HHS), SENATE
2012 · third_quarter · Medical/Disease Research/Clinical Labs
H.R. 1897 Alzheimer's Breakthrough Act of 2011, All sections H.R. 610 Making Investments Now for Dementia Act of 2011, All sections H.R. 3497 Modernizing our Drug & Diagnostics Evaluation and Regulator Network Cures Act", All sections S. 2113 Transforming the Regulatory Environment to Accelerate Access to Treatments Act, All sections H.Res 351/S.Res 176 Supporting a Semipostal Stamp to Support Medical Research Relating to Alzheimer's Disease, All sections. S.Res .434 / H. Res. 120 A resolution supporting the goal of preventing and effectively treating Alzheimer's disease by the year 2025, as articulated in the draft National Plan to Address Alzheimer's Disease from the Department of Health and Human Services, All sections. S.2069/H.R.3891 Spending Reductions through Innovations in Therapies Agenda Act of 2012, All sections S.2236 Advancing Breakthrough Therapies for Patients Act of 2012, All sections S.3187 Food and Drug Administration Safety and Innovation Act / H.R.5651 Food and Drug Administration Reform Act of 2012, All sections
Client expense: $145,000 · Firm income: Not reported
Government targets: Centers For Medicare and Medicaid Services (CMS), Food & Drug Administration (FDA), HOUSE OF REPRESENTATIVES, Health & Human Services, Dept of (HHS), Natl Institutes of Health (NIH), SENATE, Veterans Affairs, Dept of (VA)
2012 · second_quarter · Medical/Disease Research/Clinical Labs
H.R. 1897 Alzheimer's Breakthrough Act of 2011, All sections H.R. 610 Making Investments Now for Dementia Act of 2011, All sections H.R. 3497 Modernizing our Drug & Diagnostics Evaluation and Regulator Network Cures Act", All sections S. 2113 Transforming the Regulatory Environment to Accelerate Access to Treatments Act, All sections H.Res 351/S.Res 176 Supporting a Semipostal Stamp to Support Medical Research Relating to Alzheimer's Disease, All sections. S.Res .434 / H. Res. 120 A resolution supporting the goal of preventing and effectively treating Alzheimer's disease by the year 2025, as articulated in the draft National Plan to Address Alzheimer's Disease from the Department of Health and Human Services, All sections. S.2069/H.R.3891 Spending Reductions through Innovations in Therapies Agenda Act of 2012, All sections S.2236 Advancing Breakthrough Therapies for Patients Act of 2012, All sections S.3187 Food and Drug Administration Safety and Innovation Act / H.R.5651 Food and Drug Administration Reform Act of 2012, All sections
Client expense: $145,000 · Firm income: Not reported
Government targets: Centers For Medicare and Medicaid Services (CMS), Food & Drug Administration (FDA), HOUSE OF REPRESENTATIVES, Health & Human Services, Dept of (HHS), Natl Institutes of Health (NIH), SENATE, Veterans Affairs, Dept of (VA)
2012 · third_quarter · Health Issues
Support the speedy implementation of the National Alzheimer's Project Act (NAPA) by HHS, and support Leaders Engaged on Alzheimer's Disease (LEAD) recommendations as to how to proceed. Support repeal of Section 6001 of the PPACA and remove all restrictions on physician-owned hospitals. (Support H.R. 1159 and H.R. 1186) Support extensive clinical trials, manufacturing inspections and post-market surveillance for all biosimilar drugs. Support higher PDUFA fees for biosimilar drugs to pay for the additional safeguards needed. Oppose federal budget cuts that would increase co-payments for home health care services under Medicare and/or Medicaid. Support all legislative and regulatory action to modernize the FDA and to speed new cures and therapies to patients. Support the Preservation of Access to Osteoporosis Testing for Medicare Beneficiaries Act of 2011 (S. 1096, H.R. 2020) Support Leaders Engaged on Alzheimer's Disease (LEAD) FY 2012 funding proposals in the amount of for $35 billion for the National Institutes of Health (NIH), $1.4 billion for the National Institute on Aging (NIA), $100 million for the Cures Acceleration Network (CAN), $11.46 million for the Alzheimer's Disease Supportive Services Program (ADSSP), $192 million for the National Family Caregiver Support Program (NFCSP), $50 million for the Lifespan Respite Care Program (LRCP), and$2.744 billion for the Food and Drug Administration (FDA), as well as $2 million for the Missing Alzheimer's Disease Patient Alert Program and $750,000 to organize and host a high-level meeting to focus on the global Alzheimer's disease crisis. Oppose proposals that would reduce Medicare payments for providers of drugs and biologics under Medicare Part B. Support the proposed Prescription Drug User Fee Act Reauthorization Agreement (PDUFA-V) now under consideration by the Congress for reauthorization. Support an extension of the Therapeutic Discovery Project Tax Credit (I.R.C. 48D). Oppose the proposed merger between pharmacy benefit managers (PBM) Medco Health Solutions (Medco) and Express Scripts, Inc. (ESI), including comments to the Federal Trade Commission on the merger's obvious danger to older Americans. Support the development of clearly-defined, comprehensive, patient-centric Essential Health Benefits rules under the Affordable Care Act. Support the Counterfeit Drug Penalty Enhancement Act of 2011. Joined other patient advocate organizations to urge the National Government Services to reconsider its policy regarding blanket denials under the Current Procedural Terminology (CPT) health and behavioral assessment and intervention codes (96150-96155) which restrict those medically appropriate services to Medicare beneficiaries with Alzheimer's disease. Joined other patient advocate organizations January 2012 to urge HHS to ensure that ACA "Essential Health Benefits" guidelines provide comprehensive, quality and affordable health care. This was in response to the HHS December 16, 2011 bulletin on Essential Health Benefits because the HHS bulletin did not provide adequate patient protections as intended under the ACA. Joined other patient advocate groups to support the Spending Reductions through Innovations in Therapies (SPRINT) Act (H.R. 3891 and S. 2064) Support H.R.5998, the USPSTF Transparency and Accountability Act of 2012. Support the creation of the National Center for AdvancingTranslations Sciences' (NCATS) "Discovering New Therapeutic Uses for Existing Molecules Initiative." Support the new Centers for Disease Control recommendations regarding the identification of chronic Hepatitis C infections. Urge all providers and payers to follow those same CDC recommendations. Oppose the substitution and use of unapproved and off-label drugs to treat age-related macular degeneration (AMD). Urge the Department of HHS to adopt the Advisory Council on Alzheimer's Research recommendations and ensure that the final National Alzheimer's Plan includes measures: Providing high-level, overall accountability for National Plan implementation. Recognizing and proposing a path forward to secure the public and private resources needed to achieve all of the goals. Forming robust public-private partnerships between government and industry to inform the research agenda, shorten the time and cost of developing therapies, and accelerate delivery of safe and effective treatments to individuals with Alzheimers. Fostering greater collaboration on research and other issues with international counterparts to achieve global coordination and progress toward a Global Alzheimers Action Plan. Expanding attention on early detection and diagnosis of Alzheimers disease. Ensuring access to the full array of long-term support services for special and emerging populations of people with Alzheimers disease, including younger people and those with developmental disabilities. Addressing caregivers physical and behavioral health. Expanding access to high quality, cost-effective and evidence based care and redoubling efforts to test and validate innovative care interventions. Support extensive clinical trials, manufacturing inspections and post-market surveillance for all biosimilar drugs. Support higher PDUFA fees for biosimilar drugs to pay for the additional safeguards needed. Support stiff restrictions on biosimilar "flexibility" (intentionally introducing differences to the molecule or the finished product) that adds high risk. Support distinctive labeling for safety, and install a strong track and trace system before the first biosimilar is allowed on the market. Support Congressional review and oversight to examine the National Alzheimer's Plan implementation progress.
2012 · third_quarter · Health Issues
Support the speedy implementation of the National Alzheimer's Project Act (NAPA) by HHS, and support Leaders Engaged on Alzheimer's Disease (LEAD) recommendations as to how to proceed. Support repeal of Section 6001 of the PPACA and remove all restrictions on physician-owned hospitals. (Support H.R. 1159 and H.R. 1186) Support extensive clinical trials, manufacturing inspections and post-market surveillance for all biosimilar drugs. Support higher PDUFA fees for biosimilar drugs to pay for the additional safeguards needed. Oppose federal budget cuts that would increase co-payments for home health care services under Medicare and/or Medicaid. Support all legislative and regulatory action to modernize the FDA and to speed new cures and therapies to patients. Support the Preservation of Access to Osteoporosis Testing for Medicare Beneficiaries Act of 2011 (S. 1096, H.R. 2020) Support Leaders Engaged on Alzheimer's Disease (LEAD) FY 2012 funding proposals in the amount of for $35 billion for the National Institutes of Health (NIH), $1.4 billion for the National Institute on Aging (NIA), $100 million for the Cures Acceleration Network (CAN), $11.46 million for the Alzheimer's Disease Supportive Services Program (ADSSP), $192 million for the National Family Caregiver Support Program (NFCSP), $50 million for the Lifespan Respite Care Program (LRCP), and$2.744 billion for the Food and Drug Administration (FDA), as well as $2 million for the Missing Alzheimer's Disease Patient Alert Program and $750,000 to organize and host a high-level meeting to focus on the global Alzheimer's disease crisis. Oppose proposals that would reduce Medicare payments for providers of drugs and biologics under Medicare Part B. Support the proposed Prescription Drug User Fee Act Reauthorization Agreement (PDUFA-V) now under consideration by the Congress for reauthorization. Support an extension of the Therapeutic Discovery Project Tax Credit (I.R.C. 48D). Oppose the proposed merger between pharmacy benefit managers (PBM) Medco Health Solutions (Medco) and Express Scripts, Inc. (ESI), including comments to the Federal Trade Commission on the merger's obvious danger to older Americans. Support the development of clearly-defined, comprehensive, patient-centric Essential Health Benefits rules under the Affordable Care Act. Support the Counterfeit Drug Penalty Enhancement Act of 2011. Joined other patient advocate organizations to urge the National Government Services to reconsider its policy regarding blanket denials under the Current Procedural Terminology (CPT) health and behavioral assessment and intervention codes (96150-96155) which restrict those medically appropriate services to Medicare beneficiaries with Alzheimer's disease. Joined other patient advocate organizations January 2012 to urge HHS to ensure that ACA "Essential Health Benefits" guidelines provide comprehensive, quality and affordable health care. This was in response to the HHS December 16, 2011 bulletin on Essential Health Benefits because the HHS bulletin did not provide adequate patient protections as intended under the ACA. Joined other patient advocate groups to support the Spending Reductions through Innovations in Therapies (SPRINT) Act (H.R. 3891 and S. 2064) Support H.R.5998, the USPSTF Transparency and Accountability Act of 2012. Support the creation of the National Center for AdvancingTranslations Sciences' (NCATS) "Discovering New Therapeutic Uses for Existing Molecules Initiative." Support the new Centers for Disease Control recommendations regarding the identification of chronic Hepatitis C infections. Urge all providers and payers to follow those same CDC recommendations. Oppose the substitution and use of unapproved and off-label drugs to treat age-related macular degeneration (AMD). Urge the Department of HHS to adopt the Advisory Council on Alzheimer's Research recommendations and ensure that the final National Alzheimer's Plan includes measures: Providing high-level, overall accountability for National Plan implementation. Recognizing and proposing a path forward to secure the public and private resources needed to achieve all of the goals. Forming robust public-private partnerships between government and industry to inform the research agenda, shorten the time and cost of developing therapies, and accelerate delivery of safe and effective treatments to individuals with Alzheimers. Fostering greater collaboration on research and other issues with international counterparts to achieve global coordination and progress toward a Global Alzheimers Action Plan. Expanding attention on early detection and diagnosis of Alzheimers disease. Ensuring access to the full array of long-term support services for special and emerging populations of people with Alzheimers disease, including younger people and those with developmental disabilities. Addressing caregivers physical and behavioral health. Expanding access to high quality, cost-effective and evidence based care and redoubling efforts to test and validate innovative care interventions. Support extensive clinical trials, manufacturing inspections and post-market surveillance for all biosimilar drugs. Support higher PDUFA fees for biosimilar drugs to pay for the additional safeguards needed. Support stiff restrictions on biosimilar "flexibility" (intentionally introducing differences to the molecule or the finished product) that adds high risk. Support distinctive labeling for safety, and install a strong track and trace system before the first biosimilar is allowed on the market. Support Congressional review and oversight to examine the National Alzheimer's Plan implementation progress.
2012 · second_quarter · Health Issues
H.R. 4209 Patients' Access to Treatments Act; H.R. 5 Protecting Access to Healthcare Act; S. 296 / H.R. 2245 Preserving Access to Life-Saving Medications Act; S. 2069 / H.R. 3891 Spending Reductions through Innovations in Therapies Agenda Act; H.R. 3839 Drug Shortage Prevention Act; S. 2113 Transforming the Regulatory Environment to Accelerate Access to Treatments; S. 2516 Food and Drug Administration Safety and Innovation Act; H.R. 5849 Charity Care Tax Deduction for Physicians Act of 2012
Client expense: $90,000 · Firm income: Not reported
Government targets: Centers For Medicare and Medicaid Services (CMS), HOUSE OF REPRESENTATIVES, SENATE
2012 · second_quarter · Medical/Disease Research/Clinical Labs
H.R. 1897 Alzheimer's Breakthrough Act of 2011, All sections H.R. 610 Making Investments Now for Dementia Act of 2011, All sections H.R. 3497 Modernizing our Drug & Diagnostics Evaluation and Regulator Network Cures Act", All sections S. 2113 Transforming the Regulatory Environment to Accelerate Access to Treatments Act, All sections H.Res 351/S.Res 176 Supporting a Semipostal Stamp to Support Medical Research Relating to Alzheimer's Disease, All sections. S.Res .434 / H. Res. 120 A resolution supporting the goal of preventing and effectively treating Alzheimer's disease by the year 2025, as articulated in the draft National Plan to Address Alzheimer's Disease from the Department of Health and Human Services, All sections. S.2069/H.R.3891 Spending Reductions through Innovations in Therapies Agenda Act of 2012, All sections S.2236 Advancing Breakthrough Therapies for Patients Act of 2012, All sections S.3187 Food and Drug Administration Safety and Innovation Act / H.R.5651 Food and Drug Administration Reform Act of 2012, All sections
Client expense: $190,000 · Firm income: Not reported
2012 · second_quarter · Health Issues
Monitor implementation of the Patient Protection and Affordable Care Act. (P.L. 111-148) S. 2069, Spending Reductions through Innovations in Therapies Agenda Act of 2012. H.R. 3891, Spending Reductions through Innovations in Therapies Agenda Act of 2012. S. 2113, Transforming the Regulatory Environment to Accelerate Access to Treatments. S. 2196, Congressional Health Care for Seniors Act of 2012. S. 2236, Advancing Breakthrough Therapies for Patients Act of 2012. S. 2516, Food and Drug Administration Safety and Innovation Act. S. 3295, Departments of Labor, Health and Human Services, and Education, and Related Agencies Appropriations Act, 2013. Draft, House Departments of Labor, Health and Human Services, and Education, and Related Agencies Appropriations Act, 2013. H.R. 5, Protecting Access to Healthcare Act. H.R. 452, Medicare Decisions Accountability Act of 2011. H.R. 3839, Drug Shortage Prevention Act of 2012. H.R. 4209, Patients' Access to Treatments Act of 2012. H.R. 5853, Gray Market Drug Reform and Transparency Act of 2012. H.R. 451, Healthcare Truth and Transparency Act of 2011. S. 3187, Food and Drug Administration Safety and Innovation Act. H.R. 5651, Food and Drug Administration Reform Act of 2012. H.R. 5707, Medicare Physician Payment Innovation Act of 2012. H.R. 5849, Charity Care Tax Deduction for Physicians Act of 2012. Ryans Fy2013 Budget: A Path to Prosperity: A Blueprint for American Renewal Monitor federal issues and legislation associated with health care policy.
Client expense: Not reported · Firm income: $50,000
2012 · second_quarter · Health Issues
Support the speedy implementation of the National Alzheimer's Project Act (NAPA) by HHS, and support Leaders Engaged on Alzheimer's Disease (LEAD) recommendations as to how to proceed. Support repeal of Section 6001 of the PPACA and remove all restrictions on physician-owned hospitals. (Support H.R. 1159 and H.R. 1186) Support extensive clinical trials, manufacturing inspections and post-market surveillance for all biosimilar drugs. Support higher PDUFA fees for biosimilar drugs to pay for the additional safeguards needed. Oppose federal budget cuts that would increase co-payments for home health care services under Medicare and/or Medicaid. Support all legislative and regulatory action to modernize the FDA and to speed new cures and therapies to patients. Support the Preservation of Access to Osteoporosis Testing for Medicare Beneficiaries Act of 2011 (S. 1096, H.R. 2020) Support Leaders Engaged on Alzheimer's Disease (LEAD) FY 2012 funding proposals in the amount of for $35 billion for the National Institutes of Health (NIH), $1.4 billion for the National Institute on Aging (NIA), $100 million for the Cures Acceleration Network (CAN), $11.46 million for the Alzheimer's Disease Supportive Services Program (ADSSP), $192 million for the National Family Caregiver Support Program (NFCSP), $50 million for the Lifespan Respite Care Program (LRCP), and$2.744 billion for the Food and Drug Administration (FDA), as well as $2 million for the Missing Alzheimer's Disease Patient Alert Program and $750,000 to organize and host a high-level meeting to focus on the global Alzheimer's disease crisis. Oppose proposals that would reduce Medicare payments for providers of drugs and biologics under Medicare Part B. Support the proposed Prescription Drug User Fee Act Reauthorization Agreement (PDUFA-V) now under consideration by the Congress for reauthorization. Support an extension of the Therapeutic Discovery Project Tax Credit (I.R.C. 48D). Oppose the proposed merger between pharmacy benefit managers (PBM) Medco Health Solutions (Medco) and Express Scripts, Inc. (ESI), including comments to the Federal Trade Commission on the merger's obvious danger to older Americans. Support the development of clearly-defined, comprehensive, patient-centric Essential Health Benefits rules under the Affordable Care Act. Support the Counterfeit Drug Penalty Enhancement Act of 2011. Joined other patient advocate organizations to urge the National Government Services to reconsider its policy regarding blanket denials under the Current Procedural Terminology (CPT) health and behavioral assessment and intervention codes (96150-96155) which restrict those medically appropriate services to Medicare beneficiaries with Alzheimer's disease. Joined other patient advocate organizations January 2012 to urge HHS to ensure that ACA "Essential Health Benefits" guidelines provide comprehensive, quality and affordable health care. This was in response to the HHS December 16, 2011 bulletin on Essential Health Benefits because the HHS bulletin did not provide adequate patient protections as intended under the ACA. Joined other patient advocate groups to support the Spending Reductions through Innovations in Therapies (SPRINT) Act (H.R. 3891 and S. 2064) Support H.R.5998, the USPSTF Transparency and Accountability Act of 2012. Support the creation of the National Center for AdvancingTranslations Sciences' (NCATS) "Discovering New Therapeutic Uses for Existing Molecules Initiative." Support the new Centers for Disease Control recommendations regarding the identification of chronic Hepatitis C infections. Urge all providers and payers to follow those same CDC recommendations. Oppose the substitution and use of unapproved and off-label drugs to treat age-related macular degeneration (AMD). Urge the Department of HHS to adopt the Advisory Council on Alzheimer's Research recommendations and ensure that the final National Alzheimer's Plan includes measures: Providing high-level, overall accountability for National Plan implementation. Recognizing and proposing a path forward to secure the public and private resources needed to achieve all of the goals. Forming robust public-private partnerships between government and industry to inform the research agenda, shorten the time and cost of developing therapies, and accelerate delivery of safe and effective treatments to individuals with Alzheimers. Fostering greater collaboration on research and other issues with international counterparts to achieve global coordination and progress toward a Global Alzheimers Action Plan. Expanding attention on early detection and diagnosis of Alzheimers disease. Ensuring access to the full array of long-term support services for special and emerging populations of people with Alzheimers disease, including younger people and those with developmental disabilities. Addressing caregivers physical and behavioral health. Expanding access to high quality, cost-effective and evidence based care and redoubling efforts to test and validate innovative care interventions. Support extensive clinical trials, manufacturing inspections and post-market surveillance for all biosimilar drugs. Support higher PDUFA fees for biosimilar drugs to pay for the additional safeguards needed. Support stiff restrictions on biosimilar "flexibility" (intentionally introducing differences to the molecule or the finished product) that adds high risk. Support distinctive labeling for safety, and install a strong track and trace system before the first biosimilar is allowed on the market.
2012 · second_quarter · Health Issues
Support the speedy implementation of the National Alzheimer's Project Act (NAPA) by HHS, and support Leaders Engaged on Alzheimer's Disease (LEAD) recommendations as to how to proceed. Support repeal of Section 6001 of the PPACA and remove all restrictions on physician-owned hospitals. (Support H.R. 1159 and H.R. 1186) Support extensive clinical trials, manufacturing inspections and post-market surveillance for all biosimilar drugs. Support higher PDUFA fees for biosimilar drugs to pay for the additional safeguards needed. Oppose federal budget cuts that would increase co-payments for home health care services under Medicare and/or Medicaid. Support all legislative and regulatory action to modernize the FDA and to speed new cures and therapies to patients. Support the Preservation of Access to Osteoporosis Testing for Medicare Beneficiaries Act of 2011 (S. 1096, H.R. 2020) Support Leaders Engaged on Alzheimer's Disease (LEAD) FY 2012 funding proposals in the amount of for $35 billion for the National Institutes of Health (NIH), $1.4 billion for the National Institute on Aging (NIA), $100 million for the Cures Acceleration Network (CAN), $11.46 million for the Alzheimer's Disease Supportive Services Program (ADSSP), $192 million for the National Family Caregiver Support Program (NFCSP), $50 million for the Lifespan Respite Care Program (LRCP), and$2.744 billion for the Food and Drug Administration (FDA), as well as $2 million for the Missing Alzheimer's Disease Patient Alert Program and $750,000 to organize and host a high-level meeting to focus on the global Alzheimer's disease crisis. Oppose proposals that would reduce Medicare payments for providers of drugs and biologics under Medicare Part B. Support the proposed Prescription Drug User Fee Act Reauthorization Agreement (PDUFA-V) now under consideration by the Congress for reauthorization. Support an extension of the Therapeutic Discovery Project Tax Credit (I.R.C. 48D). Oppose the proposed merger between pharmacy benefit managers (PBM) Medco Health Solutions (Medco) and Express Scripts, Inc. (ESI), including comments to the Federal Trade Commission on the merger's obvious danger to older Americans. Support the development of clearly-defined, comprehensive, patient-centric Essential Health Benefits rules under the Affordable Care Act. Support the Counterfeit Drug Penalty Enhancement Act of 2011. Joined other patient advocate organizations to urge the National Government Services to reconsider its policy regarding blanket denials under the Current Procedural Terminology (CPT) health and behavioral assessment and intervention codes (96150-96155) which restrict those medically appropriate services to Medicare beneficiaries with Alzheimer's disease. Joined other patient advocate organizations January 2012 to urge HHS to ensure that ACA "Essential Health Benefits" guidelines provide comprehensive, quality and affordable health care. This was in response to the HHS December 16, 2011 bulletin on Essential Health Benefits because the HHS bulletin did not provide adequate patient protections as intended under the ACA. Joined other patient advocate groups to support the Spending Reductions through Innovations in Therapies (SPRINT) Act (H.R. 3891 and S. 2064) Support H.R.5998, the USPSTF Transparency and Accountability Act of 2012. Support the creation of the National Center for AdvancingTranslations Sciences' (NCATS) "Discovering New Therapeutic Uses for Existing Molecules Initiative." Support the new Centers for Disease Control recommendations regarding the identification of chronic Hepatitis C infections. Urge all providers and payers to follow those same CDC recommendations. Oppose the substitution and use of unapproved and off-label drugs to treat age-related macular degeneration (AMD). Urge the Department of HHS to adopt the Advisory Council on Alzheimer's Research recommendations and ensure that the final National Alzheimer's Plan includes measures: Providing high-level, overall accountability for National Plan implementation. Recognizing and proposing a path forward to secure the public and private resources needed to achieve all of the goals. Forming robust public-private partnerships between government and industry to inform the research agenda, shorten the time and cost of developing therapies, and accelerate delivery of safe and effective treatments to individuals with Alzheimers. Fostering greater collaboration on research and other issues with international counterparts to achieve global coordination and progress toward a Global Alzheimers Action Plan. Expanding attention on early detection and diagnosis of Alzheimers disease. Ensuring access to the full array of long-term support services for special and emerging populations of people with Alzheimers disease, including younger people and those with developmental disabilities. Addressing caregivers physical and behavioral health. Expanding access to high quality, cost-effective and evidence based care and redoubling efforts to test and validate innovative care interventions. Support extensive clinical trials, manufacturing inspections and post-market surveillance for all biosimilar drugs. Support higher PDUFA fees for biosimilar drugs to pay for the additional safeguards needed. Support stiff restrictions on biosimilar "flexibility" (intentionally introducing differences to the molecule or the finished product) that adds high risk. Support distinctive labeling for safety, and install a strong track and trace system before the first biosimilar is allowed on the market.
2012 · first_quarter · Health Issues
H.R. 5 Protecting Access to Healthcare Act; S. 296 / H.R. 2245 Preserving Access to Life Saving Medications Act of 2011; H.R. 3839 Drug Shortage Prevention Act of 2012; H.R. 4209 Patients' Access to Treatments Act of 2012; S. 668 Health Care Bureaucrats Elimination Act; S. 660 PATIENTS Act of 2011; S. 2069 / H.R. 3891 Spending Reductions through Innovations in Therapies Agenda Act of 2012
Client expense: $100,000 · Firm income: Not reported
Government targets: Centers For Medicare and Medicaid Services (CMS), HOUSE OF REPRESENTATIVES, SENATE
2012 · first_quarter · Medical/Disease Research/Clinical Labs
H.R. 1897 Alzheimer's Breakthrough Act of 2011, All Sections H.R. 610 Making Investments Now for Dementia Act of 2011, All Sections H.R. 3497 Modernizing our Drug & Diagnostics Evaluation and Regulator Network Cures Act", All Sections S. 2113 Transforming the Regulatory Environment to Accelerate Access to Treatments Act, All Sections H.Res 351/S.Res 176 Supporting a Semipostal Stamp to Support Medical Research Relating to Alzheimer's Disease, All Sections S.2069/H.R.3891 Spending Reductions through Innovations in Therapies Agenda Act of 2012, All Sections. Reauthorization of the Prescription Drug User Fee Act, All Sections
Client expense: $170,000 · Firm income: Not reported
Government targets: Centers For Medicare and Medicaid Services (CMS), Food & Drug Administration (FDA), HOUSE OF REPRESENTATIVES, Health & Human Services, Dept of (HHS), Natl Institutes of Health (NIH), SENATE, Veterans Affairs, Dept of (VA)
2012 · first_quarter · Health Issues
Support the speedy implementation of the National Alzheimer's Project Act (NAPA) by HHS, and support Leaders Engaged on Alzheimer's Disease (LEAD) recommendations as to how to proceed. Support repeal of Section 6001 of the PPACA and remove all restrictions on physician-owned hospitals. (Support H.R. 1159 and H.R. 1186) Support extensive clinical trials, manufacturing inspections and post-market surveillance for all biosimilar drugs. Support higher PDUFA fees for biosimilar drugs to pay for the additional safeguards needed. Oppose federal budget cuts that would increase co-payments for home health care services under Medicare and/or Medicaid. Support all legislative and regulatory action to modernize the FDA and to speed new cures and therapies to patients. Support the Preservation of Access to Osteoporosis Testing for Medicare Benificiaries Act of 2011 (S. 1096, H.R. 2020) Support Leaders Engaged on Alzheimer's Disease (LEAD) FY 2012 funding proposals in the amount of for $35 billion for the National Institutes of Health (NIH), $1.4 billion for the National Institute on Aging (NIA), $100 million for the Cures Acceleration Network (CAN), $11.46 million for the Alzheimer's Disease Supportive Services Program (ADSSP), $192 million for the National Family Caregiver Support Program (NFCSP), $50 million for the Lifespan Respite Care Program (LRCP), and$2.744 billion for the Food and Drug Administration (FDA), as well as $2 million for the Missing Alzheimer's Disease Patient Alert Program and $750,000 to organize and host a high-level meeting to focus on the global Alzheimer's disease crisis. Oppose proposals that would reduce Medicare payments for providers of drugs and biologics under Medicare Part B. Support the proposed Prescription Drug User Fee Act Reauthorization Agreement (PDUFA-V) now under consideration by the Congress for reauthorization. Support an extension of the Therapeutic Discovery Project Tax Credit (I.R.C. 48D). Oppose the proposed merger between pharmacy benefit managers (PBM) Medco Health Solutions (Medco) and Express Scripts, Inc. (ESI), including comments to the Federal Trade Commission on the merger's obvious danger to older Americans. Support the development of clearly-defined, comprehensive, patient-centric Essential Health Benefits rules under the Affordable Care Act. Support the Counterfeit Drug Penalty Enhancement Act of 2011. Joined other patient advocate organizations to urge the National Government Services to to reconsider itspolicy regarding blanket denials under the Current Procedural Terminology (CPT) health and behavioral assessment and intervention codes (96150-96155) which restrict those medically appropriate services to Medicare beneficiaries with Alzheimer's disease. Joined other patient advocate organizations January 2012 to urge HHS to ensure that ACA "Essential Health Benefits" guidelines provide comprehensive, quality and affordable health care. This was in response to the HHS December 16, 2011 bulletin on Essential Health Benefits because the HHS bulletin did not provide adequate patient protections as intended under the ACA. Joined other patient advocate groups to support the Spending Reductions through Innovations in Therapies (SPRINT) Act (H.R. 3891 and S. 2064)
2012 · first_quarter · Health Issues
Monitor implementation of the Patient Protection and Affordable Care Act. (P.L. 111-148) S. 660, PATIENTS Act of 2011. S. 668, Health Care Bureaucrats Elimination Act. S. 1031, Medicaid Improvement and State Empowerment Act. H.R. 2013, Medicaid Improvement and State Empowerment Act. S. 2069, Spending Reductions through Innovations in Therapies Agenda Act of 2012. H.R. 3891, Spending Reductions through Innovations in Therapies Agenda Act of 2012. S. 2113, Transforming the Regulatory Environment to Accelerate Access to Treatments. S. 2196, Congressional Health Care for Seniors Act of 2012. H.R. 5, Protecting Access to Healthcare Act. H.R. 452, Medicare Decisions Accountability Act of 2011. H.R. 1173, Fiscal Responsibility and Retirement Security Act of 2011. H.R. 3399, Medicare and Medicaid FAST Act. H.R. 3630, Temporary Payroll Tax Cut Continuation Act of 2011. (P.L. 112-96) H.R. 3839, Drug Shortage Prevention Act of 2012. H.R. 4209, Patients' Access to Treatments Act of 2012. Ryans Fy2013 Budget: A Path to Prosperity: A Blueprint for American Renewal Monitor federal issues and legislation associated with health care policy.
Client expense: Not reported · Firm income: $50,000
2012 · first_quarter · Health Issues
H.R. 3590 - Patient Protection and Affordable Care Act / Public Law 111-148; track and monitor implementation; and S. 2069 / H.R. 3891, Spending Reductions through Innovation in Therapies Agenda Act of 2012.
Client expense: Not reported · Firm income: $50,000
Government targets: Centers For Medicare and Medicaid Services (CMS), HOUSE OF REPRESENTATIVES, SENATE
2012 · first_quarter · Health Issues
Support the speedy implementation of the National Alzheimer's Project Act (NAPA) by HHS, and support Leaders Engaged on Alzheimer's Disease (LEAD) recommendations as to how to proceed. Support repeal of Section 6001 of the PPACA and remove all restrictions on physician-owned hospitals. (Support H.R. 1159 and H.R. 1186) Support extensive clinical trials, manufacturing inspections and post-market surveillance for all biosimilar drugs. Support higher PDUFA fees for biosimilar drugs to pay for the additional safeguards needed. Oppose federal budget cuts that would increase co-payments for home health care services under Medicare and/or Medicaid. Support all legislative and regulatory action to modernize the FDA and to speed new cures and therapies to patients. Support the Preservation of Access to Osteoporosis Testing for Medicare Beneficiaries Act of 2011 (S. 1096, H.R. 2020) Support Leaders Engaged on Alzheimer's Disease (LEAD) FY 2012 funding proposals in the amount of for $35 billion for the National Institutes of Health (NIH), $1.4 billion for the National Institute on Aging (NIA), $100 million for the Cures Acceleration Network (CAN), $11.46 million for the Alzheimer's Disease Supportive Services Program (ADSSP), $192 million for the National Family Caregiver Support Program (NFCSP), $50 million for the Lifespan Respite Care Program (LRCP), and$2.744 billion for the Food and Drug Administration (FDA), as well as $2 million for the Missing Alzheimer's Disease Patient Alert Program and $750,000 to organize and host a high-level meeting to focus on the global Alzheimer's disease crisis. Oppose proposals that would reduce Medicare payments for providers of drugs and biologics under Medicare Part B. Support the proposed Prescription Drug User Fee Act Reauthorization Agreement (PDUFA-V) now under consideration by the Congress for reauthorization. Support an extension of the Therapeutic Discovery Project Tax Credit (I.R.C. 48D). Oppose the proposed merger between pharmacy benefit managers (PBM) Medco Health Solutions (Medco) and Express Scripts, Inc. (ESI), including comments to the Federal Trade Commission on the merger's obvious danger to older Americans. Support the development of clearly-defined, comprehensive, patient-centric Essential Health Benefits rules under the Affordable Care Act. Support the Counterfeit Drug Penalty Enhancement Act of 2011. Joined other patient advocate organizations to urge the National Government Services to reconsider its policy regarding blanket denials under the Current Procedural Terminology (CPT) health and behavioral assessment and intervention codes (96150-96155) which restrict those medically appropriate services to Medicare beneficiaries with Alzheimer's disease. Joined other patient advocate organizations January 2012 to urge HHS to ensure that ACA "Essential Health Benefits" guidelines provide comprehensive, quality and affordable health care. This was in response to the HHS December 16, 2011 bulletin on Essential Health Benefits because the HHS bulletin did not provide adequate patient protections as intended under the ACA. Joined other patient advocate groups to support the Spending Reductions through Innovations in Therapies (SPRINT) Act (H.R. 3891 and S. 2064)
| Democratic |
| NJ |
Client expense: $75,187 · Firm income: Not reported
Government targets: Centers For Medicare and Medicaid Services (CMS), Federal Trade Commission (FTC), Food & Drug Administration (FDA), HOUSE OF REPRESENTATIVES, Health & Human Services, Dept of (HHS), SENATE
Client expense: Not reported · Firm income: $9,625
Government targets: Centers For Medicare and Medicaid Services (CMS), Federal Trade Commission (FTC), Food & Drug Administration (FDA), HOUSE OF REPRESENTATIVES, Health & Human Services, Dept of (HHS), SENATE
Government targets: Centers For Medicare and Medicaid Services (CMS), Food & Drug Administration (FDA), HOUSE OF REPRESENTATIVES, Health & Human Services, Dept of (HHS), Natl Institutes of Health (NIH), SENATE, Veterans Affairs, Dept of (VA)
Government targets: HOUSE OF REPRESENTATIVES, SENATE
Client expense: Not reported · Firm income: $10,808
Government targets: Centers For Medicare and Medicaid Services (CMS), Federal Trade Commission (FTC), Food & Drug Administration (FDA), HOUSE OF REPRESENTATIVES, Health & Human Services, Dept of (HHS), SENATE
Client expense: $61,150 · Firm income: Not reported
Government targets: Centers For Disease Control & Prevention (CDC), Centers For Medicare and Medicaid Services (CMS), Federal Trade Commission (FTC), Food & Drug Administration (FDA), HOUSE OF REPRESENTATIVES, Health & Human Services, Dept of (HHS), SENATE
Client expense: $83,191 · Firm income: Not reported
Government targets: Centers For Medicare and Medicaid Services (CMS), Federal Trade Commission (FTC), Food & Drug Administration (FDA), HOUSE OF REPRESENTATIVES, Health & Human Services, Dept of (HHS), SENATE
Government targets: HOUSE OF REPRESENTATIVES, SENATE
Client expense: Not reported · Firm income: $12,238
Government targets: Centers For Medicare and Medicaid Services (CMS), Federal Trade Commission (FTC), Food & Drug Administration (FDA), HOUSE OF REPRESENTATIVES, Health & Human Services, Dept of (HHS), SENATE