On behalf of the Parenteral Drug Association (PDA), we are pleased to submit comments on the Current Good Manufacturing Practice Requirements for Combination Products, Docket No. (f/k/a FDA-2008-D-0409]; extension of comment period Docket FDA-2009-N-0435-004]. Please note that this is the second attempt from PDA in that the "browse" and "attached" button froze and failed before the actual documentation was submitted.
FDANonrulemakingFDA-2009-N-0435
Current Good Manufacturing Practice Requirements for Combination Products-CLOSED
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Parenteral Drug Association filings
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Parenteral Drug Association filed 1 comment on this docket between Feb 4, 2010 and Feb 4, 2010. 0 other organizations filed here. The comment window closed 6017d ago.
What Parenteral Drug Association filed (1)
Feb 4, 2010· Parenteral Drug Association (PDA) - Comment· FDA-2009-N-0435-0017
Abstract
September 23, 2009 (74 FR 48423) FR document published with an incorrect docket number. This FR document was published to correct the Docket ID (FDA-2008-D-0409) 78 FR 4307 Eff.date 7/22/2013, Rules and Regulations published which closed the docket
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