Featured Issue Briefs

The Battle on the Home Front: Jonathan Gadsden's Story

The Battle on the Home Front: Jonathan Gadsden's Story

Marine Lance Corporal's story reflects the growing need for new antibiotics that can treat dangerous diseases, against which most drugs are useless. Read More

Facilitating Medical Device Innovation: De Novo Reform

Facilitating Medical Device Innovation: De Novo Reform

The de novo process -- which requests lower-risk reclassification of medical devices and entry into the marketplace -- as it exists now is not achieving its purpose and has instead added unnecessary and time-consuming requirements. Read More

Food Products Recalled by FDA

Food Products Recalled by FDA

Since President Obama signed the FDA Food Safety Modernization Act into law, at least 149 FDA-regulated food products have been recalled due to potential pathogenic contamination. Read More

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Date Issue Briefs Topic
Dec 15, 2008

Non-physician Prescribers and Pharmaceutical Industry Interactions

Industry marketing to non-physician prescribers has increased markedly in recent years to roughly 20 million detail visits in 2006, a 20% increase over 2004.

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Conflicts of Interest

Jul 17, 2012

Obama needs to release draft food safety rules, say victims and advocacy groups

The U.S. Centers for Disease Control and Prevention estimate that one in six Americans (48 million people) suffer from a foodborne illness each year, resulting in 128,000 hospitalizations and 3,000 deaths. Americans will continue to get sick and even die from foodborne disease as your Administration continues to hold up the food safety rules. In fact, the U.S Food and Drug Administration (FDA) essentially ensured such an outcome last week in a letter to food industry representatives. In it, the FDA said that until final rules are issued, the agency would not enforce the FSMA requirements that food processors adopt prevention-based protections, and that importers assure the safety of the food products they send to the United States.

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School Food, Food Hazards

Jul 14, 2010

Official Text: Hearing on Antibiotic Resistance and the use of Antibiotics in Animal Agriculture

The CDC lists control over infectious disease as one of its top 10 great public health achievements of the last century, and antimicrobials are crucial to that accomplishment. And yet we must collectively be alarmed that we are undermining the power of antibiotics by failing to use them judiciously.

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Antibiotics in Food Animal Production

Oct 1, 2007

Overview of Child Welfare Services in Michigan State

Michigan is experiencing severe economic and fiscal problems due primarily to a downturn in the automobile industry, resulting in a budget deficit of approximately $856.4 million at the end of the state's 2007 fiscal year (September 30).  Because of these issues, many of the state's budget bills are still being debated as of the date of this memo.  The human services budget bill, SB 232, was passed by the Senate on August 22, 2007.  The House passed an amended version of the bill on September 6, 2007.  The bill is currently in conference committee.  This memo will summarize those provisions in the bills that are relevant to reform of federal child welfare financing.  When a budget is finally approved and signed by the Governor, this memo will be updated. 

 

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Health Topics

Dec 6, 2007

Overview of Child Welfare Services in Montana

Child welfare services in Montana are administered by Child and Family Services Division (CFSD) within the Montana Department of Public Health and Human Services.  Recent events and initiatives of note are the federal CFSR in 2002 and resulting PIP, completed successfully in 2006, and a study of the child welfare system in the summer of 2006 by the legislative Children, Families, Health and Human Services Interim Committee.  Both of these events have focused attention on child welfare in Montana. 

 

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Health Topics

Jan 1, 2008

Overview of Child Welfare Services in Ohio State

Ohio's child welfare system is state-supervised and county-administered.  A number of recent developments and converging trends may have a significant impact on child welfare financing in Ohio.

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Health Topics

Sep 3, 2007

Overview of Child Welfare Services in Tennessee State

Tennessee's child welfare system has undergone dramatic changes over the past few years.  Throughout the 1980s and early 1990s, child welfare in Tennessee was under-funded and fragmented among six state agencies that failed to communicate with one another or coordinate their efforts.  In 1996, a single state agency, the Department of Children's Services (DCS) was created by executive order to house child welfare and juvenile justice services.  In 2000, Children's Rights, a national non-profit that advocates for children in foster care, filed a class action lawsuit, claiming over-utilization of emergency shelters and large group facilities, untrained caseworkers, high levels of placement instability, inadequate efforts to achieve permanency, inadequate educational services and disparate treatment of African-American children in foster care.

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Health Topics

Jul 2, 2007

Overview of Child Welfare Services in Washington State

Compared to other states, child welfare is high on the list of legislative priorities in Washington.  This high level of legislative activity can be attributed in part to a number of recent events that are briefly described below.  In addition, the legislature, particularly the House, has a number of experienced champions of children's issues, including Rep. Ruth Kagi, chair of the House Early Learning and Children's Services Committee, and Rep. Mary Lou Dickerson, chair of the House Human Services Committee, among others. 

 

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Health Topics

Jan 2, 2012

Patient Story: Jamel Sawyer: A Young Man Fights MRSA

One of the most notorious multidrug-resistant superbugs, MRSA is responsible for an estimated 19,000 deaths and 360,000 hospitalizations each year in this country. Jamel’s story illustrates the twin dangers presented by emerging multidrug-resistant bacterial infections and the waning effectiveness and availability of drugs to treat them.

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Antibiotic Innovation

Jul 20, 2012

Pew Asks FDA to Close Loopholes in New Guidelines to Protect Antibiotics From Overuse

Pew's Laura Rogers, program director of the Human Health and Industrial Farming initiative, commended the U.S. Food and Drug Administration (FDA) for issuing Draft Guidance 213 for industry on antibiotics in animal feed and water and urged the agency to consider improvements that would better protect public health. More

Antibiotics in Food Animal Production

Jul 20, 2012

Pew Asks FDA to Strengthen Guidelines on Antibiotic Use in Food Animals

Pew's Human Health and Industrial Farming team has applauded the U.S. Food and Drug Administration (FDA) for issuing Guide 209. However, they would like to see additional strengthening measures, which can help begin the process of making progress toward reducing the development and spread of antibiotic-resistant bacterial infections in people. More

Antibiotics in Food Animal Production

Aug 23, 2012

Pew Biomedical Scholar Profile: Sohini Ramachandran

Sohini Ramachandran, a population geneticist at Brown University in Providence, Rhode Island, received two high-profile awards this year. In June, she was named a Pew Scholar in Biomedical Sciences by the Pew Charitable Trusts, based in Philadelphia, Pennsylvania; and in February, she received a fellowship from the Alfred P. Sloan Foundation in New York. She plans to use the grants to distinguish herself in a fast-moving field. More

Biomedical Research

Jun 7, 2013

Pew Comment Letter to the Senate HELP Committee on Compounding Legislation

Pew sent a comment letter to the Senate Committee on Health, Education, Labor and Pensions on the Pharmaceutical Compounding Quality and Accountability Act. This bill takes steps toward clarifying state and federal oversight of compounding, including an important increase in FDA supervision of certain activities—specifically, the compounding of sterile medicines that are shipped interstate.

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Drug Manufacturing and Distribution, Drug Safety

Nov 21, 2012

Pew Comments on Advance Notice of Proposed Rulemaking ''Antimicrobial Animal Drug Sales and Distribution Reporting''

The Pew Campaign on Human Health and Industrial Farming submitted a letter to the U.S. Food and Drug Administration, urging the FDA to strengthen regulations pertaining to record-keeping and public reporting of antibiotic use in food animal production. More

Antibiotics in Food Animal Production

Apr 9, 2013

Pew Comments on Centers for Medicaid and Medicare Services' Information Collection Activities Draft Guidance

The Pew Charitable Trusts appreciates this opportunity to submit comments to CMS's "Information Collection Activities" draft guidance. We suggest that both the research and non-research payment templates be modified in order to make it easier for consumers to identify which drugs, devices, biologicals, or medical supplies are associated with particular transfers of value.

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Aug 3, 2012

Pew Comments on Draft Guidance for Industry Regarding Nanotechnology in Food

The Food Additives Project of the Pew Health Group strongly agrees with the FDA's draft decision to deny "generally recognized as safe" (GRAS) status to nanoengineered chemicals and review them as food additives. However, they list their concerns with certain aspects of the document and question the agency's claim that it has not reviewed GRAS notifications sanctioning the use of nanoengineered chemicals. More

Food Additives

Apr 4, 2013

Pew Comments on Draft Recommendations for Meaningful Use, Stage 3

The Pew Charitable Trusts submitted comments on preliminary recommendations regarding Stage 3 meaningful use objectives and standards for electronic health records (EHRs) to the Office of the National Coordinator for Health Information Technology. These comments follow remarks at recent meetings of the Health Information Technology (HIT) Policy Committee and HIT Standards Committee.

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Nov 8, 2012

Pew Comments to the FDA Regarding the Unique Device Identification System

Pew’s Medical Device Initiative, along with the American Heart Association and Trust for America’s Health, submitted comments to the U.S. Food and Drug Administration (FDA) regarding its proposed rule for a unique device identification (UDI) system for medical devices. Once implemented by the FDA and utilized by healthcare providers, the UDI system will be the cornerstone for significant improvements in postmarketing surveillance of medical devices.

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Drugs and Devices at the FDA

Feb 17, 2012

Pew Health Group comments on the implementation of Section 6002 of the Patient Protection and Affordable Care Act

"The Pew Health Group of The Pew Charitable Trusts welcomes the opportunity to submit comments regarding the Centers for Medicare & Medicaid Services' ("CMS") proposed rule for Medicare, Medicaid, Children's Health Insurance Programs; Transparency Reports and Reporting of Physician Ownership or Interests."

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Conflicts of Interest

Jul 21, 2009

Pew letter to the FDA in response to their public recognition of animal agriculture's contribution to antimicrobial resistance

The Pew Campaign on Human Health and Industrial Farming (Pew) would like to extend our sincere thanks to you both for taking the time to meet with us on June 23 to discuss the contribution of animal agriculture to the growing public health crisis of antimicrobial resistance. We are deeply appreciative not only of your consideration of our viewpoints, but also the expertise and dedication that you bring to the U.S. Food and Drug Administration (FDA).

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Antibiotics in Food Animal Production

Jul 20, 2012

Pew Seeks More Veterinary Oversight of Antibiotic Use on Industrial Farms

Gail Hansen, a senior officer with the Pew Health Group, thanks the U.S. Food and Drug Administration (FDA) for issuing draft codified language expanding the Veterinary Feed Directive (VFD). She also raises several concerns with the language that should be addressed. More

Antibiotics in Food Animal Production

Mar 10, 2010

Pew Statement on Energy and Commerce Drug Safety Hearing

"Two years after dozens of Americans lost their lives to contaminated heparin, we are still unable to protect U.S. consumers from many of the risks of pharmaceuticals manufactured in foreign factories. It is time for Congress to take action to better protect health."

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Drug Manufacturing and Distribution, Drug Safety

May 9, 2013

Pew Testimony on the Safety of Compounding Pharmacies

The U.S. Senate Committee on Health, Education, Labor and Pensions held a hearing on May 9 entitled "Pharmaceutical Compounding: Proposed Legislative Solution." Pew's Allan Coukell, a pharmacist and drug safety expert, testified on the need to strengthen oversight of the compounding industry.

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Apr 25, 2013

Pew Testimony to House Energy and Commerce Subcommittee on Health Regarding Drug Supply Chain

The House Energy & Commerce Subcommittee on Health will hold a hearing on April 25 entitled "Securing Our Nation’s Prescription Drug Supply Chain." Allan Coukell, a pharmacist and drug safety expert, will testify on the need to establish a national system to track and authenticate medicine. The principles outlined in his prepared testimony are supported by other stakeholders in statements from consumer, patient, public health, and industry groups.

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Drug Manufacturing and Distribution, Drug Safety

May 23, 2013

Pew Testimony: Examining Drug Compounding

On Thursday, May 23, the House Energy & Commerce Subcommittee on Health held a hearing, entitled "Examining Drug Compounding." Gabrielle Cosel, a drug safety expert, testified on the need to clarify oversight of compounding pharmacies on the state and federal level.

 

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Drug Manufacturing and Distribution, Drug Safety