Articles tagged with “21-cfr-part-820”

Veeva Vault QMS: CAPA Implementation & Configuration Guide

Configure CAPA management in Veeva Vault QMS with this technical guide. Covers data models, 21 CFR Part 820 compliance, and workflow implementation steps.

40 min read

2/21/2026

veeva vault qms capa management 21 cfr part 820 quality management system root cause analysis iso 13485 capa configuration life sciences quality audit trails regulatory compliance

Veeva Vault QMS: ISO 13485 Compliance for Medical Devices

Examine how Veeva Vault QMS supports ISO 13485 compliance for medical devices. Learn to map digital QMS features to regulatory standards for audit readiness.

25 min read

2/18/2026

veeva vault qms iso 13485 medical device qms 21 cfr part 820 digital quality management regulatory compliance audit readiness design controls