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Current
Good Manufacturing Practice Issues on Human Use Pharmaceuticals
HUMAN DRUG CGMP NOTES is a periodic memo for
FDA personnel on Current Good Manufacturing Practice Issues on Human
Use Pharmaceuticals, issued by the Division of Manufacturing and Product
Quality, HFD-320, Office of Compliance, Center for Drug Evaluation
and Research, U.S. Food and Drug Administration, 7520 Standish Place,
Rockville, MD 20855.
Human Drug CGMP Notes -2000
September 2000
June 2000
March 2000
Human Drug CGMP Notes -1999
September 1999
June 1999
March 1999
Human
Drug CGMP Notes - 1998
December
1998
September
1998
June
1998
March
1998
Human Drug CGMP Notes -1997
December
1997
September
1997
June
1997
March
1997
Human Drug CGMP Notes -1996
December
1996
September
1996
June
1996
March
1996
Human Drug CGMP Notes -1995
December
1995
September
1995
June
1995
March
1995 |
