21 CFR Part 211 of US describes the 'Current Good Manufacturing Practices (cGMP)' for pharmaceutical industry. This is deemed to be dynamic, so that updated principles can be facilitated for implementation.
Dear Nirmal Kumar,
General home-page for 21 CFR Part 211 from FDA site is:
https://www.fda.gov/drugs/pharmaceutical-quality-resources/current-good-manufacturing-practice-cgmp-regulations
In this page you can find most actual 21 CFR Part 211 content:
https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?CFRPart=211
But in header of the page FDA inform:
" The information on this page is current as of April 1 2019. For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR)."
This sentence cover active link for CRF which redirect into this site:
https://www.ecfr.gov/cgi-bin/text-idx?SID=3ee286332416f26a91d9e6d786a604ab&mc=true&tpl=/ecfrbrowse/Title21/21tab_02.tpl
Next you can go to CRF 200-299 parts:
https://www.ecfr.gov/cgi-bin/text-idx?SID=c95f59020a7c0f43313637e3a89639a7&mc=true&tpl=/ecfrbrowse/Title21/21cfrv4_02.tpl#0
And for 211 sub-part:
https://www.ecfr.gov/cgi-bin/text-idx?SID=c95f59020a7c0f43313637e3a89639a7&mc=true&node=pt21.4.211&rgn=div5
"Source: 43 FR 45077, Sept. 29, 1978, unless otherwise noted." In header you can find information that " e-CFR data is current as of October 18, 2019"
Hope it helps
Best regards
Tomasz
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