How to Adapt to an eQMS With Ease

Course Overview

Many pharma companies are slow to adopt newer technologies and have a legacy of paper-based systems. Consequently, maintaining compliance with evolving GMP regulations is becoming extremely challenging. For this reason, any pharma and medical device manufacturer must implement an Electronic Quality Management System (eQMS) as soon as possible. However, if not approached correctly, the transition from a paper-based system to eQMS can be long, painful, and quite expensive. 

To make the transition to an eQMS as quick and efficient as possible, you need to plan it well and have the proper roadmap.

In this webinar, you’ll learn how to make a smooth, fast transition to an eQMS by avoiding the common technical pitfalls and personnel-related frustrations that can make the transition unnecessarily challenging.

The speaker, Kelly Stanton, has guided many companies with their paper to an eQMS transition. During this webinar, she will walk you through the practical and straightforward process of eQMS implementation, give tips for success, and share case studies allowing you to learn from the triumph stories of other organizations. 

Most importantly, you will get a step-by-step guideline on creating your roadmap to a successful eQMS implementation.