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Surviving early biotech pitfalls

 – Overcoming challenges when moving from non-clinical to clinical

When: May 27th
Time: 10:00 to 11:30 CET
Place: Digital webinar

Register here


Going from non-clinical to clinical is no easy step. Join our free webinar on May 27th and listen to a few of our key experts from essential product development areas to talk about how to survive and minimize the early risks biotech companies face during the life-cycle of product development. We have a complete panel of experienced experts who will go through key elements to consider in the clinical development process.

This event is designed to help biotech companies in early development however, the content will also be helpful for the full life cycle of a product. View the agenda below to learn more.

* Please kindly note that this event is not for competitor service providers.


9:45 The Meeting opens up for early login
10:00 Introduction of team
10:05 Factors to consider when selecting a manufacturer.
The value of a GMP audit
Hilde Ringstad, Director Quality Assurance and Compliance
10:15 CMC/IMPD
Crucial CMC regulatory compliance strategy In early biotech
Lone Dyrby, Regulatory Director – Denmark
Pipeline strategy; Clinical trials and their relative value inflection points
Austin Smith,  VP Clinical Development, Oncology specialist
The value of Scientific advice
Marie Moores, EVP Clinical Operations
10:45 Biostatisticians early in the design
Christina Ehrenkrona
10:55 The importance of proper data handling
Mario Baban, EDC Group Manger
11:05 Clinical Trial Safety
Tina Elberling,  Director Safety International Operations
Open Q/A


Read more about our speakers and event details here.

Register here

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