FDAnews Announces Webinar on Quality, Compliance and Validation in the Age of Digital Transformation Sponsored by Axendia and Tulip March 8, 2022


Life Sciences Digital Transformation Made Easy: Discuss Quality, Compliance and Validation with this free webinar. register today

FALLS CHURCH, Va., March 1, 2022 /PRNewswire-PRWeb/ — Quality, Compliance and Validation in the Age of Digital Transformation
An Axendia Industry webinar presented by Tulip
Tuesday, March 8, 2022, 11:00 a.m. – 12:00 p.m. EST
https://us02web.zoom.us/webinar/register/9216427090367/WN_Rb459_q3TSeyRCRCYXfqhA

Digital transformation in the life sciences is no longer an asset, it’s a must.

With the productivity gains that will be realized – coupled with the digital acceleration brought about by COVID-19 – changing course is a business imperative.

This webinar has answers. This will eliminate the fear of transformation and allow you to modernize systems and culture with new approaches to quality, compliance and validation.

Add to that the formation and structure of the new FDA Office of Digital Transformation; this signals the serious stance the agency is taking on digital transformation.

But you need to be careful. You cannot successfully implement modern technology based on regulatory guidelines that are over 20 years old. Example: how do you balance the flexibility of modern no-code platforms with the rigidity of outdated CSV procedures?

As regulators undergo their own digital transformations – and urge life sciences companies to do the same – it’s time to push forward.

Daniel R. Matlis, Chairman and Founder of Axendia; Head of Client Services and Head of Life Sciences Practice at Tulip Gilad Langer, doctorate; and Tulip’s quality manager, Michelle Vuolowill explain how life sciences companies can make much-needed digital transformations more manageable and less daunting.

Takeaways from the webinar:

● The value and benefits of moving to the new digital paradigm and especially moving away from the “document mindset”
● The difference between digital platforms and traditional electronic or paper-on-glass (POG) systems
● How to make validation and compliance transparent with digital platforms (focusing on what is important)
● How to make the Pharma 4.0 operating model a reality in your company (transformations go beyond digital tools!)

Webinar details:
Quality, Compliance and Validation in the Age of Digital Transformation
An Axendia Industry webinar presented by Tulip
Tuesday, March 8, 2022, 11:00 a.m. – 12:00 p.m. EST
https://us02web.zoom.us/webinar/register/9216427090367/WN_Rb459_q3TSeyRCRCYXfqhA

Easy ways to register:
Online: https://us02web.zoom.us/webinar/register/9216427090367/WN_Rb459_q3TSeyRCRCYXfqhA
By phone: 888.838.5578 or 703.538.7600

About FDAnews:
FDAnews is the premier provider of domestic and international regulatory, legislative and business news and information for executives in industries regulated by the US FDA and European Medicines Agency. Pharmaceutical and medical device industry professionals rely on FDAnews’ print and electronic newsletters, books, and conferences to stay compliant with international standards and complex, ever-changing FDA regulations.

Media Contact

Michael ButlerFDAnews, 703.538.7600, [email protected]

SOURCEFDA news

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