How to Choose a Quality Management System for a FDA-regulated Environment

Description: 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

To view the recorded webinar, please fill out the form below. For more information, feel free to call us on 650-620-2955/2935 or email us at info@metricstream.com