How to choose a Quality Management System for a FDA-regulated environment
Duration: 1 Hour
Many Pharmaceutical, Bio-Tech and Medical Device companies are finding that their home grown or spreadsheet-based Quality Management System has become an impediment to their growth.
Such systems come apart at their seams as companies grow, resulting in a high risk of non-compliance with cGMP and 21CFR Part 11 regulations
In this webinar, the presenters will review:
The key requirements of a 21CFR Part 11 compliant Quality Management System
Demonstrate key capabilities such as -
- Document Control
- Deviations
- CAPA
- Management Dashboards
Panelist(s) Info:
Akshay Gahlot - Business Development Manager FDA Compliance and Regulations
Raj Munaim - Senior Solutions Manager
Register to View this Recorded Webinar
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