Good Documentation Practices Medical Devices

https://www.fda.gov/medical-devices/quality-system-qs-regulationmedical-device-good-manufacturing-practices/medical-devices-current-good-manufacturing-practice-cgmp-final-rule-quality-system-regulation

The FDA is revising the current good manufacturing practice (CGMP) requirements for medical devices and incorporating them into a quality system regulation.

“Do’s and Don’ts” of Medical Device Good …

https://qaconsultinginc.com/dos-and-donts-of-medical-device-good-documentation-practices/

Good Documentation Practices and Compliance. While there is no industry requirement to follow GDP, ISO 13485 and 21 CFR 820 require documents to be legible, …

Good Documentation Practices - RAPS

https://www.raps.org/RAPS/media/Publications-Resources/Sample-Chapter/Regulatory-Writing-An-Overview-Second-Edition-Sample-Chapter-1.pdf

Good Documentation Practices (GDPs) are essential in any professional setting and critical in regulated medical device, drug, and biological product environments. In …

Good Documentation Practices (GDocP)

https://www.pharmout.net/good-documentation-practices-gdocp-gmp/

Good documentation practice (GDocP) is a crucial component of GMP compliance. Also referred to …