The world's leading automated proofreading software

Future Proof Your Regulatory Submissions for Global Compliance

Published By:

Peter Muller
< 1 minute read
Generic selectors
Exact matches only
Search in title
Search in content
Post Type Selectors

Table of Contents

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, Schlafender Hase

Peter Muller
Sales Director North America
Schlafender Hase Inc

LinkedIn Profile

David Wilson, Reed Tech

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.

Share this article

Peter Muller profile picture

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.

Learn More

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, Schlafender Hase

Peter Muller
Sales Director North America
Schlafender Hase Inc

LinkedIn Profile

David Wilson, Reed Tech

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.

Past Webinars

August 8, 2024

Schlafender Hase Team

The Role of Barcodes in Life Sciences, and the Key to Ensuring Barcode Accuracy

As the world shifts towards electronically delivered e-Labeling, it's essential to stay ahead of the game. Regulatory Authorities are now permitting and encouraging online e-PIL content, with other regions follow suit.

< 1 minute read

The Role of Barcodes in Life Sciences, and the Key to Ensuring Barcode Accuracy

As the world shifts towards electronically delivered e-Labeling, it's essential to stay ahead of the game. Regulatory Authorities are now permitting and encouraging online e-PIL content, with other regions follow suit.

May 31, 2024

Schlafender Hase Team

Embracing e-Labeling in a global context

As the world shifts towards electronically delivered e-Labeling, it's essential to stay ahead of the game. Regulatory Authorities are now permitting and encouraging online e-PIL content, with other regions follow suit.

2 minutes read

Embracing e-Labeling in a global context

As the world shifts towards electronically delivered e-Labeling, it's essential to stay ahead of the game. Regulatory Authorities are now permitting and encouraging online e-PIL content, with other regions follow suit.

January 17, 2024

Schlafender Hase Team

TOPRA Sponsored Webcast: A Non-Technical AI Introduction for Regulatory Affairs Professionals

AI is already being used in many Life Science applications, meanwhile Health Authorities are looking to regulate the use of AI. As a regulatory affair professional, it is essential to have an understanding of this technology.    In this general introduction to the field of AI, different uses of the term "Artificial Intelligence" will be discussed, and which might be desirable in a given context. 

2 minutes read

TOPRA Sponsored Webcast: A Non-Technical AI Introduction for Regulatory Affairs Professionals

AI is already being used in many Life Science applications, meanwhile Health Authorities are looking to regulate the use of AI. As a regulatory affair professional, it is essential to have an understanding of this technology.    In this general introduction to the field of AI, different uses of the term "Artificial Intelligence" will be discussed, and which might be desirable in a given context.