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Future Proof Your Regulatory Submissions for Global Compliance

Published By:

Peter Muller

< 1 minute read

Play Video about Webinar: Future Proof your Regulatory Submissions for Global Compliance

Original Broadcast Date: March 3, 2022
Length: 35 minutes

Overview:

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)

Takeaway:

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

Presenters:

Peter Muller
Sales Director North America
Schlafender Hase Inc

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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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Peter Muller

Director - Americas at Schlafender Hase

For over 25 years, Peter Muller has worked on software and process improvement projects relating to proofreading with Fortune 500 companies from various industries: Pharmaceutical, Medical Device & Consumer Goods.

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Subscribe to our blog

Play Video about Webinar: Future Proof your Regulatory Submissions for Global Compliance

Original Broadcast Date: March 3, 2022
Length: 35 minutes

Overview:

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)

Takeaway:

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

Presenters:

Peter Muller
Sales Director North America
Schlafender Hase Inc

LinkedIn Profile

David Wilson
Sr. Account Executive
Reed Tech

LinkedIn Profile

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.

Subscribe to our blog

Follow Us

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< 1 minute read

The Game-Changing Features of TVT 12: A New Era in Compliance and Efficiency

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2 minutes read

Learning the New Language of the EMA & The FDA: FHIR

Watch our interactive discussion session focusing on the evolution and outlook of Fast Healthcare Interoperability Resources (FHIR). FHIR represents a significant step in how we manage and exchange information and is rapidly gaining acceptance. In this session, industry experts will provide an introduction to the FHIR initiative, explore some current applications as well as the impacts, benefits and prospective timelines.