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 EMA Publishes Revised Guideline on Evaluating Antibacterial Drugs May 25, 2022 EMA Outlines Methods for Transferring Product Approvals Before Brexit November 28, 2017 Takeda Strengthens Its CAR-T Platform With GammaDelta Therapeutics Acquisition October 28, 2021