Eugia Pharma Specialties Warning Letter Cites Incomplete Test Data, Inaccurate Records

Failure to conduct complete testing on sterile injectables, falsified monitoring records of areas used for aseptic filling lines as well as falsified cleaning records are among the serious lapses documented in the FDA’s Aug. 15 Warning Letter to Eugia Pharma Specialties of Hyderabad, Telangana, India.
Source: Drug Industry Daily

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