
FDA's Francis R.W. Godwin (CDER) and Kathleen Jones, PhD (CBER) detail a record pace of drug warning letters and the CGMP deficiencies most commonly cited in biologics facility inspections.
Click the title above to open the BioPharm International July 2017 issue in an interactive PDF format.
about 9 years ago
Laboratory Data Integrity Benefits from Electronic Systemsabout 9 years ago
Do You Listen to What Your Data are Telling You?about 9 years ago
Matching Tools to Biophysical Analysis Demandsabout 9 years ago
Tale of Two Financial Trendsabout 9 years ago
Inspections: The Value of the Opening Presentationabout 9 years ago
Balancing Protocols for Leachablesabout 9 years ago
Biosafety Concerns of Single-Use Componentsabout 9 years ago
FDA Continues to Promote Quality Drug Production





