Webinars on demand

Cell therapy logistics is challenged by complex processes, inefficiency, and lack of flexibility to accommodate manufacturing, clinic, and patient needs

Upstream process intensification efforts are becoming mainstream in every biopharma R&D lab and clinical program.

With this webinar we pretend to look at the different sorts of impurities that may occur in pharmaceutical products and discuss current regulations, requirements and control strategies to be followed in order to comply with the current demands.

Join Thermo Fisher Scientific’s drug development and clinical services experts for another Q&A session to hear about the company’s innovation.

Join Thermo Fisher Scientific’s drug development and manufacturing experts for a unique, extended Q&A session and learn how to start navigating the new normal.

The cell and gene therapy regulatory landscape is rapidly evolving. Join this webinar to discover the approaches available to this industry to accelerate the approval of cell and gene therapy products.

Join us for an informative webinar on May 26 at 10am EDT / 4pm CEST as we discuss the advantages of DBcaps®.

This webinar will give viewers the tools they need to initiate a close examination of their methods.

Is there a case for re-evaluating cell viability in bioprocesses?

Find out how new operating systems for the industrial Internet of Things can enable flexible, open connectivity solutions for physical infrastructure

A facility’s balance between supporting initial product demand and future projections is essential.

A report on the first large-scale comparison of glycoanalytical techniques for mAb characterization in industry and academia.