Difference between revisions of "21 CFR Part 11"
From LIMSWiki
Jump to navigationJump to searchm (Made some terms links.) |
m (added category) |
||
| Line 1: | Line 1: | ||
The Title 21 Code of Federal Regulations (21 CFR Part 11) provides compliance information regarding [[Electronic Records]] and [[Electronic Signatures]]. Within this part, requirements are set forth to help insure security, integrity, and confidentially of [[electronic records]] and to insure that [[electronic signatures]] are as legally binding as hand-written signatures. For more information, refer to the [http://www.fda.gov/ U.S Food and Drug Administration Web site] and search for 21 CFR Part 11. | The Title 21 Code of Federal Regulations (21 CFR Part 11) provides compliance information regarding [[Electronic Records]] and [[Electronic Signatures]]. Within this part, requirements are set forth to help insure security, integrity, and confidentially of [[electronic records]] and to insure that [[electronic signatures]] are as legally binding as hand-written signatures. For more information, refer to the [http://www.fda.gov/ U.S Food and Drug Administration Web site] and search for 21 CFR Part 11. | ||
[[Category:Regulatory information]] | |||
Revision as of 18:33, 22 April 2011
The Title 21 Code of Federal Regulations (21 CFR Part 11) provides compliance information regarding Electronic Records and Electronic Signatures. Within this part, requirements are set forth to help insure security, integrity, and confidentially of electronic records and to insure that electronic signatures are as legally binding as hand-written signatures. For more information, refer to the U.S Food and Drug Administration Web site and search for 21 CFR Part 11.
