How to Adapt to an eQMS With Ease


16:00 - 17:30


Feb 09 2022

Learning Type

Free Live Webinar



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. 

Register now, and as a bonus, you will also get a PDF whitepaper detailing the process so that you can begin working on your roadmap straight away.

  • Who Should Attend:
    • Quality Managers and VPs
    • Manufacturing Leads
    • Validation experts
    • Natural-Sciences Startup Founders/CEOs.
  • Skill Level: Novice, Intermediate
  • Topics:
    • A roadmap to a successful transition from paper-based QMS to an electronic one
    • How to pick the right people to lead the transition 
    • How to choose which processes to carry over from the paper-based system 
    • How to set reasonable deadlines 
    • How to turn reluctant users into software advocates
    • Discussion and Q&A


  • Kelly Stanton
    Kelly Stanton
    Director of Quality at Qualio

    Kelly brings over 20 years of experience in both the pharmaceutical and medical device industry to the world of small start-ups and scalable quality system implementations. Having been an implementer, administrator, and user of many different eQMS tools on the market, she has built several quality systems. Kelly is an advisor to over 20 Medical Device and Pharma companies. She is currently the Director of Quality at Qualio, helping customers and the company adheres to the evolving regulatory landscape. She leads a team of talented industry-experienced quality professionals who work daily with companies in regulated industries.




Founded in 2012, Qualio is the first cloud quality management software for all Life Sciences companies. Medical device and pharmaceutical companies need a secure and scalable quality management system with the flexibility to support their evolving needs. Qualio meets that challenge by cutting through the complexity to optimize and automate critical quality processes. The remote-first, Qualio team is distributed across North America and Europe.

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Event Registration

Local Time

  • Timezone: Asia/Singapore
  • Date: Feb 09 - 10 2022
  • Time: 23:00 - 00:30

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If you attend the live session you will get a digital certificate of attendance emailed to you within 7-working days. 

Yes, our event partners will email you the event recording within several weeks. 

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