Observed multiple problems with documentation

Reference no: EM133198197 , Length: 1 Pages

1. During an inspection of New Drug Biologics, the FDA inspector observed multiple problems with documentation and quality oversight that are a violation of current good manufacturing practices (cGMPs). Based on the Week 9 readings, what is the process for notifying New Drug Biologics of these observations? How is New Drug Biologics able to respond after they have been notified of the observations?

If I were a competitor of New Drug Biologics, would I be able to find out what the FDA observed during the inspection? If so, how?

2. Does the source of funding for clinical research affect the outcome/results of the trial?

Reference no: EM133198197

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