Future proof your regulatory submissions for global compliance
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.
Original broadcast date: March 3, 2022
Length: 35 minutes
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 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. He has a wealth of experience working with international clients to define their organization’s goals and help them leverage new technologies to achieve productivity gains, process improvements and cost savings.
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David Wilson
Sr. Account Executive at Reed Tech
