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The revised ISO 15189 | ISO 15189 compliance
In this webinar, we have explored best practice for when companies are transitioning to the recently revised ISO 15189:2022 standard.
Watch Dr David Ricketts and Stephen Ferrell, experts on the standard, as they give you all the tools you will need to ensure your lab’s compliance and deep dive into the changes, refinements and key risk factors in the revised validation and verification process requirements.
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key takeaways
What you will learn
- Ensuring your lab’s compliance with the new changes.
- The key risk factors in the revised validation and verification process.
- How the revised ISO 15189:2022 has framed risk and opportunity.
About this webinar
Discover Risk, validation & the revised ISO 15189 Program
With a greater emphasis on risk as one of the main changes in the new standard, the webinar also focuses on how ISO 15189:2022 frames risk and opportunity.
Meet our speaker
David Ricketts
Founder, David Ricketts Consultancy LimitedDavid Ricketts has extensive experience in writing standards and leading ISO projects, including the ISO 15189 revision.
Stephen Ferrell
Chief Product Officer, Valkit.aiStephen Ferrell is Chief Product Officer at Valkit.ai, a leading provider of validation and compliance solutions for the pharmaceutical industry. With over 25 years of experience in pharmaceutical quality systems and computerized system validation, Stephen has helped hundreds of companies navigate complex regulatory requirements while implementing innovative technology solutions. He was a contributing author to ISPE GAMP 5 2nd edition, as well as a number of other ISPE guides and industry publications.
FAQ
Frequently asked questions
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