The world's leading automated proofreading software

The Schlafender Hase Team

Future Proof Your Regulatory Submissions for Global Compliance

Play Video about Webinar: Future Proof your Regulatory Submissions for Global Compliance
Original Broadcast Date: March 3, 2022
Length: 35 minutes


Data Management is an integral part of regulatory compliance across the globe. There are many nuances to consider including information storage, change management, and measurable evolution of harmonious systems.

Reed Tech and Schlafender Hase are industry leaders that work together to help ensure Life Sciences companies and their products comply with regulatory standards.

Join us for a discussion focusing on these topics and how they are affected by Health Authority regulations.


Key Learning Points:

  • Advice on how to centralize, store and consolidate data

  • Strategies to help any size organization put the right RIM process in place

  • Possibilities of and best practices for Information Management Systems (RIM, LIM, CCDS etc.)

  • What is harmonious evolution: Learn the different ways to store and repurpose your data to meet the latest requirements of new regulations from local to global health authorities (FDA, Health Canada)


Introduction to key concepts of regulatory data management to facilitate growth and scalability.


Peter Muller, Schlafender Hase

Peter Muller
Sales Director North America
Schlafender Hase Inc

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David Wilson, Reed Tech

David Wilson
Sr. Account Executive
Reed Tech

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Do you want to find out more about how your proofreading life can be easier? Get in touch and we’ll tell you all about it.

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