Draft Guidance for Industry on Residual Solvents in Drug Products Marketed in the United States; Availability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
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AstraZeneca - Comment
Posted : 09/30/2008 ID :FDA-2008-D-0413-0003 Agency : FDA -
Jan 01,0001 12:00 AM ET
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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
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sanofi-aventis - Comment
Posted : 10/03/2008 ID :FDA-2008-D-0413-0005 Agency : FDA -
Jan 01,0001 12:00 AM ET
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Covidien - Comment
Posted : 10/04/2008 ID :FDA-2008-D-0413-0006 Agency : FDA -
Jan 01,0001 12:00 AM ET
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Pfizer, Inc. - Comment
Posted : 10/07/2008 ID :FDA-2008-D-0413-0007 Agency : FDA -
Jan 01,0001 12:00 AM ET
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IPEC - Comment
Posted : 10/07/2008 ID :FDA-2008-D-0413-0008 Agency : FDA -
Jan 01,0001 12:00 AM ET
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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
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BASF Corporation (BC) - Comment
Posted : 10/08/2008 ID :FDA-2008-D-0413-0010 Agency : FDA -
Jan 01,0001 12:00 AM ET
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Schering Plough Corporation - Comment
Posted : 10/08/2008 ID :FDA-2008-D-0413-0011 Agency : FDA -
Jan 01,0001 12:00 AM ET
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Yannick Lefevre (PCAS) - Comment
Posted : 10/10/2008 ID :FDA-2008-D-0413-0012 Agency : FDA -
Jan 01,0001 12:00 AM ET
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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
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Teva Parenteral Medicines - Comment
Posted : 10/30/2008 ID :FDA-2008-D-0413-0014 Agency : FDA -
Jan 01,0001 12:00 AM ET