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
