Draft Guidance for Industry on Residual Solvents in Drug Products Marketed in the United States; Availability

Document ID: FDA-2008-D-0413-0001

Comments

Total: 12
AstraZeneca - Comment
Posted : 09/30/2008     ID :FDA-2008-D-0413-0003     Agency : FDA

Jan 01,0001 12:00 AM ET
SOCMA's Bulk Pharmaceuticals Task Force - Comment
Posted : 10/01/2008     ID :FDA-2008-D-0413-0004     Agency : FDA

Jan 01,0001 12:00 AM ET
sanofi-aventis - Comment
Posted : 10/03/2008     ID :FDA-2008-D-0413-0005     Agency : FDA

Jan 01,0001 12:00 AM ET
Covidien - Comment
Posted : 10/04/2008     ID :FDA-2008-D-0413-0006     Agency : FDA

Jan 01,0001 12:00 AM ET
Pfizer, Inc. - Comment
Posted : 10/07/2008     ID :FDA-2008-D-0413-0007     Agency : FDA

Jan 01,0001 12:00 AM ET
IPEC - Comment
Posted : 10/07/2008     ID :FDA-2008-D-0413-0008     Agency : FDA

Jan 01,0001 12:00 AM ET
International Pharmaceutical Excipients Council of the Americas - Comment
Posted : 10/07/2008     ID :FDA-2008-D-0413-0009     Agency : FDA

Jan 01,0001 12:00 AM ET
BASF Corporation (BC) - Comment
Posted : 10/08/2008     ID :FDA-2008-D-0413-0010     Agency : FDA

Jan 01,0001 12:00 AM ET
Schering Plough Corporation - Comment
Posted : 10/08/2008     ID :FDA-2008-D-0413-0011     Agency : FDA

Jan 01,0001 12:00 AM ET
Yannick Lefevre (PCAS) - Comment
Posted : 10/10/2008     ID :FDA-2008-D-0413-0012     Agency : FDA

Jan 01,0001 12:00 AM ET
Pharmaceutical Research and Manufacturers of America (PhRMA) - Comment
Posted : 10/16/2008     ID :FDA-2008-D-0413-0013     Agency : FDA

Jan 01,0001 12:00 AM ET
Teva Parenteral Medicines - Comment
Posted : 10/30/2008     ID :FDA-2008-D-0413-0014     Agency : FDA

Jan 01,0001 12:00 AM ET