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CGA M-16

$17.00

Standard for Food, Drug, and Medical Device Gas and Gas Equipment Manufacturers on Electronic Records and Signatures
Handbook / Manual / Guide by Compressed Gas Association, 02/23/2022

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Description

This publication is based on FDA’s August 2003 Guidance for Industry Part 11, Electronic Records; Electronic Signatures–Scope and Application and satisfies the criteria of 21 CFR Part 11, § 11.1 (a) “The regulations in this part set forth the criteria under which the agency considers electronic records, electronic signatures, and handwritten signatures executed to electronic records to be trustworthy, reliable, and generally equivalent to paper records and handwritten signatures executed on paper”.

This guideline also harmonizes with PIC/S Guide for good manufacturing practice for medicinal products, Annex 11 “Computerised Systems” (as adopted in Canada).

Product Details

Edition:
2
Published:
02/23/2022
Number of Pages:
16
File Size:
1 file , 380 KB
Note:
This product is unavailable in Belarus, Russia, Ukraine
Sale!

CGA M-16

$36.00

Guidance for Electronic Records and Signatures in the U.S. and Canadian Food, Drug, and Medical Device Gas and Gas Equipment Industry
Handbook / Manual / Guide by Compressed Gas Association, 03/01/2016

  • Disc PDF Format
  • Disc MULTI-USER
  • Disc NOTE: Our website provide PDF immediately download, sometimes when the payment is processed and you did not receive the file, please feel free to connect with us.
GUARANTEED SAFE CHECKOUT
  • Visa Card
  • MasterCard
  • American Express
  • Discover Card
  • PayPal
Category:

Description

This guideline is based upon FDA’s August 2003 Guidance for Industry Part 11, Electronic Records; Electronic Signatures—Scope and Application and satisfies the criteria of 21 CFR Part 11, § 11.1 (a) “The regulations in this part set forth the criteria under which the agency considers e-records, e-signatures, and handwritten signatures executed to e-records to be trustworthy, reliable, and generally equivalent to paper records and handwritten signatures executed on paper”.

This guideline also harmonizes with PIC/S Guide for good manufacturing practice for medicinal products, Annex 11 “Computerised Systems” (as adopted in Canada).

Product Details

Edition:
1st
Published:
03/01/2016
Number of Pages:
16
File Size:
1 file , 260 KB