Bioprocessing Webinar: Single-Use Systems - A Prerequisite for Closed Processing in Final Filtration and Filling Operation

The rapid expansion in biopharmaceutical manufacturing capacity has increased the demand for SUS. Key drivers are flexibility, quick changeover of equipment, and reducing the risk of contamination when operating as closed systems. Join us to learn about regulatory expectations when implementing SUS. 

In this webinar, you will learn:

• Regulatory expectations when implementing and using single-use systems
• Quality control of single-use systems - shift of responsibility from end-user to supplier
• How single-use systems enable closed processing

Speaker

Dr. Simone Biel  
Senior Regulatory Consultant, Regulatory Affairs

Simone is our Senior Regulatory Consultant and provides regulatory and scientific expertise to our customers and internal stakeholders globally with a focus on Single-Use Technology. With her deep understanding of Single-Use Technology market needs and industry trends, she is the subject matter expert to ensure that product performance meets quality and regulatory requirements. Simone holds a Ph.D. from the University of Frankfurt in Microbiology.

Moderator

Jayesh Parkar
Regional Strategy Execution Manager, Single Use Technologies

Jayesh leads the Single Use and Integrated Systems Regional Strategic Execution activities for Asia Pacific ex-China and has been with Merck for 12 years. His expertise include Biopharma Industry association activities in the Single Use space & execution of Strategic Projects for Merck. During his tenure at Merck, his work involved in various functions across the Pharma & Bioprocessing space in Formulation, Upstream & Single Use technologies. Prior to working at Merck, he studied the Post-Graduate program in Management at the Indo-German Chamber of Commerce & has received a MS in Life Sciences with specialization in Biotechnology.