The world's leading automated proofreading software

The Schlafender Hase Team

Innovator Rx Drug Product Labeling: From Creation to Change Management


Calling all Regulatory Affairs in life sciences, pharmaceutical and medical device industries

This webinar will help companies understand the nuances of global health authority drug product labeling requirements.

Original Broadcast Date: Thursday, October 20, 2022 
Duration: 60 minutes

The featured speakers will explore what research is needed to meet these requirements, how to conduct this research in the most efficient manner and how to create and submit labels. The speakers will further discuss how companies can quickly and accurately verify labels and manage future version changes of labels, documents and submissions.

Next, they will examine ways to centralize label change management to better plan, track, curate and support ongoing regulatory label compliance. Finally, the webinar will explain how to intelligently reuse label content data across regions.

Watch now to join a panel of regulatory experts and learn about pharma labeling from the basics and beyond! Topics covered range from global health authority label requirements through the practical process of completing, submitting and continuing to manage drug product labeling.

Attendees will gain insights into:
  • Global health authority label requirements

  • Label research and creation

  • Label comparison and verification

  • Change management and global labeling orchestration

Who Should Attend?
  • Regulatory Affairs and Operation Leaders

  • Manufacturing

  • Operations and Supply Chain Leaders

  • Global Strategy Business Managers

  • Compliance Officers

  • Product Managers

  • Business Analysts


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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January 17, 2024

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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. 

August 23, 2023

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How to Build a Business Case for Document Comparison Software: A Step-by-Step Buyer’s Guide

Join Schlafender Hase on September 14th, as we guide you through the typical steps needed to properly identify the right tool for your organization and how to get it approved.

June 27, 2023

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Digital transformation is all the rage these days, but what does that actually mean for professionals working with regulated content in Pharma and Med Device, and more importantly, what does it mean for you? Join us on November 10th as we explore the why and how of a digital proofreading workflow.