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Date: September 2, 2025

Time: 10am ET / 4pm CET

Summary

As a formulation scientist, you’re under constant pressure to deliver fast, reliable results – especially when facing formulation changes, scale-ups, or site transfers. These challenges can trigger costly and time-consuming clinical studies, delaying timelines and increasing risk. IVIVC studies offer a regulatory-accepted path to secure biowaivers and minimize the need for in-vivo bioequivalence testing.

The Phoenix® IVIVC Toolkit is designed specifically for formulation scientists to simplify and accelerate the development of IVIVC models. This powerful software enables you to reduce clinical study requirements, speed up development timelines, and increase confidence in regulatory submissions.

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What to expect in the webinar

  • Discover how the Phoenix IVIVC Toolkit supports IVIVC study design and analysis
  • Learn about its regulatory acceptance and typical use cases
  • Watch a live demo of the toolkit in action
  • See a real-world case study showing how a formulation team used Phoenix IVIVC to successfully support a biowaiver

Who should attend

Formulation scientists, biopharmaceutics professionals, regulatory teams

Register now