https://www.fda.gov/drugs/postmarket-drug-safety-information-patients-and-providers/fda-statement-voluntary-withdrawal-raptiva-us-market
FDA Statement on the Voluntary Withdrawal of Raptiva From the U.S. Market | FDA
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https://www.biocon.com/update-on-company-statement-on-us-fda-inspection-at-biocon-malaysia/
Update on Company Statement on US-FDA Inspection at Biocon Malaysia - Biocon
company statementus fdaupdateinspectionbiocon
https://www.citizen.org/article/statement-to-fda-hearing-on-saline-breast-implants/
Statement to FDA Hearing on Saline Breast Implants - Public Citizen
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https://a4pc.org/news/apc-on-503b-glp1-proposal
Statement from the Alliance for Pharmacy Compounding on FDA Proposed Rule Regarding 503B Bulks List
Apr 30, 2026 - APC is reviewing the FDA’s proposed rule addressing the 503B Bulks List, including the proposal not to include liraglutide, semaglutide, and tirzepatide.