FDA Hits Aesica Over Quality Controls, Record-Keeping Post author:Sam Post published:April 19, 2017 Post category:Drug Industry Daily The FDA has cited contract manufacturer Aesica for quality and record-keeping problems. Source: Drug Industry Daily You Might Also Like EU Makes Biosimilars Officially Interchangeable, While FDA Ponders and Awaits Funds September 20, 2022 TGA Announces Overhaul of Drug Advertising Regulations March 14, 2018 Skyhawk Teams With Sanofi on Oncology and Immunology Targets in Deal Worth Potentially $2 Billion July 6, 2022
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