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FREE ON-DEMAND WEBINAR
March 8, 2023
The Ugly Truth About Paper-Based QMS - Making the Switch to eQMS
MedTech companies face heavier regulation requirements than ever before, and an increasing need to ensure traceability within their system processes.
Yet, many companies have chosen to maintain their Quality Management System with antiquated documentation on paper, or in generic tools like Sharepoint, Google Docs, or Dropbox.
This outdated approach to a QMS is hard to manage, slows down the product development process, and creates massive inefficiencies within a company. Despite this, many companies are reluctant to make a change and modernize their QMS because it may seem too daunting.
This webinar will highlight why MedTech companies should be concerned about what tools they use to maintain traceability - from an economical, regulatory, and ethical standpoint, and how to make the switch to an eQMS without disrupting the current process.
Join us as we speak with several companies who have successfully migrated from paper to an eQMS. They will share their migration stories and the positive impact it has had on their business.
Watch the webinar
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Specifically, this webinar will help you:
- Identify when you're ready to make the switch
- Understand the impact an eQMS can have on speed and efficiency in your company
- Learn how to prove the ROI of switching to your organization
- Discover best practices for a successful eQMS implementation
Who should attend?
- Regulatory Affairs Professionals & Management
- Quality Professionals and Management
- Medical Device Executives
- Product Development Engineers and Management
- Complaint and CAPA Management & Professionals
