'Not scientifically supportable:' Inside FDA's refusal to face US generic drug crisis
DeLauro backed a proposal for the Defense Department to buy drugs independently rated as low risk and criticized the FDA’s oversight.

SOURCE CHECK
TAP FOR WHYCredibility rates Wpde, which republished this story. The other scores rate the article itself.
The report names its authors and includes interviews with an outside expert and an agency response, supporting some transparency. The publisher is a local outlet, but the available information does not establish its corrections practices or broader reporting record.
- Source type — WPDE is presented as a local news publisher; no more specific source classification is available.
- Author attribution — Three reporters are named.
- Editorial standards — The report includes attributed interviews and the FDA's written response, though it is strongly framed around criticism of the agency.
- Transparency — The article describes the reporters' interview request and the agency's response, but offers limited information about the outlet's policies.
The report includes a named expert, congressional statements and the FDA's response, and describes the agency's opportunity to comment. The FDA's position is represented mainly through a written statement, while the article gives substantially more space to critics and provides limited independent evidence or competing context.
HOW WE SCORE ↗The report includes the FDA's stated position and its response to the reporters, but most of the detailed discussion comes from critics of the agency. The FDA's direct response to the specific questions was unavailable by deadline, leaving the article weighted toward one perspective.
- Counterarguments presented — The FDA's general position is quoted, but the report says it did not directly answer the reporters' questions.
- Source diversity — The report includes a physician-researcher, two lawmakers and an agency statement, but detailed evidence and argument chiefly come from critics.
- Omitted context — The report gives limited context supporting the FDA's position or explaining the agency's oversight practices.
The report is sharply critical of the FDA's handling of generic-drug oversight, but that framing does not establish a discernible left-right political lean. Its focus is regulatory oversight and drug safety rather than partisan politics.
- Language tone — The framing emphasizes criticism of the FDA, but does not use clear partisan language.
- Source selection — Most interview material comes from critics of the FDA, while the agency's position is included in a written statement.
- Framing — The report foregrounds a dispute over regulatory oversight without a clear partisan frame.
Republished
Republished from WJLA. The relationship between the two publishers has not been determined.
14 stories · 74–77 · updated Oct 6, 2026
This is WJLA's own score, and this article is credited to WJLA. The host score in the Source Check is Wpde's.
WPDE reports that the FDA is reaffirming its position that generic drugs meet brand-name quality standards despite criticism from researchers and investigators. A bipartisan bill from Representatives Rosa DeLauro and Rich McCormick would require the Defense Department to buy drugs independently rated as low risk for manufacturing problems and contaminants.
The report says the FDA has reiterated that generic drugs must meet the same quality and safety standards as brand-name medicines. It describes a bipartisan bill from Representatives Rosa DeLauro and Rich McCormick that would require the Defense Department to purchase drugs independently identified as low risk for manufacturing mistakes and contaminants. DeLauro criticized the FDA’s oversight and said people should have a right to know what is in their medicines.
Dr. Arthur Kellermann, an emergency physician and co-author of research on generic drugs, said the FDA’s claims were not scientifically supportable and criticized its reliance on periodic factory inspections and manufacturers’ paperwork. The FDA said generic drugs must meet the same standards for approval, quality, safety and effectiveness as brand-name drugs. The agency did not answer the reporters’ questions directly before the story’s deadline.
Community verdict
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SWIPE →Representative and proponent of the proposed drug-purchasing legislation
Representative and co-sponsor of the proposed drug-purchasing legislation
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