The world's leading automated proofreading software

Future Proof Your Regulatory Submissions for Global Compliance

Published By:

Peter Muller

< 1 minute read

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.

Share this article

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.

Follow Us

Categories

Categories

Subscribe to our blog

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

Categories

Past Webinars

May 29, 2025

Schlafender Hase Team

RAPS Webinar: e-Labeling and what it means for Regulatory Teams

E-labeling is no longer a future concept. Regulatory agencies worldwide, including the EMA, FDA, and MHRA, are advancing digital product information initiatives. But what does this mean for your daily work as a regulatory professional? How will your submission and labeling processes change? And how can you prepare today to avoid last-minute compliance risks?

2 minutes read

RAPS Webinar: e-Labeling and what it means for Regulatory Teams

E-labeling is no longer a future concept. Regulatory agencies worldwide, including the EMA, FDA, and MHRA, are advancing digital product information initiatives. But what does this mean for your daily work as a regulatory professional? How will your submission and labeling processes change? And how can you prepare today to avoid last-minute compliance risks?

May 26, 2025

Schlafender Hase Team

TVT Integration: Connect, Automate, Accelerate

Learn how new custom integration capabilities make it easy to connect TVT with the systems you already use; enabling greater automation, reducing manual effort, and accelerating review processes, all while maintaining the precision and compliance standards you rely on.

< 1 minute read

TVT Integration: Connect, Automate, Accelerate

Learn how new custom integration capabilities make it easy to connect TVT with the systems you already use; enabling greater automation, reducing manual effort, and accelerating review processes, all while maintaining the precision and compliance standards you rely on.

May 22, 2025

Schlafender Hase Team

Precision Talks: Optimizing Packaging Workflows with Compliance and Innovation

Join Chris Janczar from Esko and Marc Chaillou from Schlafender Hase for an exclusive discussion on how automation and digital maturity can transform your packaging workflows. This session is designed for professionals who are responsible for optimizing workflows, approving artworks, and reducing risk in their packaging process.

< 1 minute read

Precision Talks: Optimizing Packaging Workflows with Compliance and Innovation

Join Chris Janczar from Esko and Marc Chaillou from Schlafender Hase for an exclusive discussion on how automation and digital maturity can transform your packaging workflows. This session is designed for professionals who are responsible for optimizing workflows, approving artworks, and reducing risk in their packaging process.