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Allan Coukell


Senior Director, Drugs and Medical Devices , The Pew Charitable Trusts
Headshot Coukell 435 full

To reach this expert, please contact:

Elizabeth Butler
Administrative Assistant
202-540-6578
ebutler@pewtrusts.org

Allan Coukell is the senior director of drugs and medical devices, including the prescription project, the drug safety project, the antibiotics and innovation project, the medical device initiative and the FDA modernization initiative, as well as other activities related to medical products and services.

He leads the drug safety project's advocacy around the need for reforms to address the risks of the global pharmaceutical manufacturing and distribution supply chain. He has also contributed to the development of federal and state legislation to foster transparency of physician-industry relationships and in the creation of programs to encourage evidence-based prescribing. He has worked closely with medical schools and medical centers developing new industry relations policies, and was co-creator of the American Medical Student Association PharmFree Scorecard, a national assessment of  such policies at U.S. medical schools.

Coukell practiced as a clinical pharmacist in oncology at the Victoria Hospital and London Regional Cancer Center in London, Ontario and was subsequently a senior medical writer and editor with Adis International, publisher of the peer-reviewed journals DrugsDrugs & Aging, and PharmacoEconomics, among others.

He also spent a decade in journalism, ultimately as health and science reporter for WBUR, Boston’s NPR news station. He was the founding producer and host of the weekly Eureka! science program on Radio New Zealand, and has written for The Economist, the New York TimesNew Scientist and Discover, among other publications. He is the recipient of an Edward R Murrow award for hard news reporting.

Allan Coukell serves as the consumer representative on the FDA Cardiovascular and Renal Drugs Advisory Committee.

News

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''Senate Panel Approves Tighter Oversight of Compounding Pharmacies, but Bill is Under Fire''

Media Coverage

Public health and consumer advocacy groups are attacking Senate legislation designed to tighten oversight of specialized pharmacies such as the one at the center of this past fall’s deadly meningitis outbreak, saying it does not adequately address health risks.

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''Rep. Bob Latta's Plan to Thwart Fake Drugs Passes House of Representatives Committee''

Media Coverage
An Ohio legislator’s plan to establish a nationwide prescription drug tracking system to protect patients from fake drugs was approved by the House Commerce Committee. More

''Drug Manufacturer Agrees to $500 Million Penalty''

Media Coverage

''A subsidiary of India's largest pharmaceutical company has agreed to pay a record $500 million in fines and penalties for selling adulterated drugs and lying to federal regulators in a case that is part of an ongoing crackdown on the quality of generic drugs flowing into the U.S."

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Events

After Heparin: A Roundtable on Ensuring the Safety of the U.S. Drug Supply

Event
The Pew Charitable Trusts hosted a roundtable discussion addressing the safety of the U.S. drug supply. Expert presentations were part of a larger conversation on the issues and solutions raised in a draft white paper entitled, After Heparin: Protecting Consumers from the Risks of Substandard and Counterfeit Drugs. More


Resources

Pew Testimony on the Safety of Compounding Pharmacies

Issue Brief

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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Testimony of Allan Coukell Before the Committee on Commerce, Science and Transportation

Issue Brief

Pew's Allan Coukell submitted a statement of record to the Congressional Committee on Commerce, Science and Transportation regarding concerns with the pharmaceutical supply chain. The focus of Coukell's testimony was the drug distribution system – the weaknesses in the system and the risks of counterfeit and stolen drugs.

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Facilitating Medical Device Innovation: De Novo Reform

Issue Brief
The de novo process as it exists now is not achieving its purpose of streamlining the path to move new devices onto the marketplace and has instead added unnecessary and time-consuming requirements. More


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