Pharma and Med Device Regulations
<1 min read
by Peter Muller

Innovator Rx drug product labeling: from creation to change management

Pharma and Med Device Regulations
2 min read
by Peter Muller
Webcast: e-PIL legislation will have a positive impact on patient safety and sustainability

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 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

Source: https://xtalks.com/webinars/innovator-rx-drug-product-labeling-101-from-creation-to-change-management/

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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