In this free webinar, learn about the annual deadlines that pharmaceutical companies are required to fulfill to become and remain compliant with the US Food and Drug Administration (FDA). Attendees who are a part of regulatory teams will learn the best way to navigate these annual requirements and ensure they are complying with all year-end deadlines. The featured speakers will discuss annual deadlines, year-end requirements, Structured Product Labeling (SPL) requirements, new REMS (Risk Evaluation and Mitigation Strategy) in SPL deadline, and data storage and management.
TORONTO, Aug. 30, 2022 /PRNewswire-PRWeb/ -- This webinar will take a complete look at the annual deadlines that pharmaceutical companies are required to fulfill to become and remain compliant with the US Food and Drug Administration (FDA).
The webinar is designed to help regulatory teams understand the best way to navigate these annual requirements and ensure they are complying with all year-end deadlines.
Attendees will gain insights into the following takeaways: Overview of annual deadlines; Year-end requirements; Structured Product Labeling (SPL) requirements; New REMS (Risk Evaluation and Mitigation Strategy) in SPL deadline; Data storage and management; And frequently asked questions.
Join the featured speakers, Reed Tech subject-matter experts David Wilson and Julia Frasch, as they explore how pharmaceutical companies can navigate through structured product labeling requirements and other new guidelines.
Join experts from Reed Tech, David Wilson, Pharma Team Lead; and Julia Frasch, Pharma Account Executive, for the live webinar on Wednesday, September 21, 2022, at 2pm EDT (11am PDT).
For more information, or to register for this event, visit Risk Evaluation and Mitigation Strategies in Structured Product Labeling Format and Additional Pharma Annual Deadlines.
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