Abstract

A fully GMP-/GDP-compliant and smooth drug supply is key for every clinical trial. But it can also easily turn into a bumpy ride without proper expertise and planning.
To provide reliable solutions and address the related challenges, in-depth knowledge of the product, of the GMP-relevant supply chain, and of the study set-up is required.

Join us live to discuss the specific challenges associated with the design and conduct of your drug supply from manufacturing, importation, blinding and packaging to distribution to the clinical sites.

In this 45-minute webinar, Dr. Christin Erbach, Head of Global Clinical Trial Supplies at NUVISAN will cover the following topics:

• Complex supply chains
• Blinding challenges
• Costly medication solutions
• Achieving QP release
• Distribution obstacles
• Live Q&A session

In a Q&A session following this case study presentation, it will be possible to discuss further on these or any other topics of interest.

Can't join? Don't worry, register anyway, the slides and recording will be sent to you after the webinar.