Biotech Integrated Solutions - Accelerate Speed to Market
Scaling gene therapy, mAb, or vaccine therapeutic drug products from bench to manufacturing involves a balancing act between project management, risk mitigation, and process parameter selection. A holistically-executed development that takes these into consideration can help identify and mitigate risks before they occur and protect the project budget – ultimately accelerating speed to market.
Join our Technical Director, Kevin Thompson, as he explores the ways Pall Corporation applies best practices through implementation of the Biotech Integrated Solutions service architecture for large-scale manufacturing projects.
Global Product Manager, Integrated Solutions
Dave is a Global Product Manager covering the Integrated Solutions program, responsible for marketing operations, outbound marketing and customer research. He joined us in 2016, bringing 11 years of both scientific and engineering experience in the areas of product development, project management, R&D and marketing. He holds degrees in both Microbiology and Mechanical Engineering from the University of Massachusetts, Amherst.
Technical Director, Pall Advanced Separation Systems (PASS)
Kevin is a Technical Director within the PASS team - a customer-focused process engineering and project management team responsible for delivering integrated solutions to the pharmaceutical industry. He has spent the last 40 years in Engineering, starting in the UK’s electrical supply industry, transitioning to Oil and Gas, followed by Chemicals and Polymers, with the last 22 years dedicated to Pharmaceuticals. He is located within our Center of Excellence in Portsmouth, UK, where he manages a group of project managers - process and commissioning engineers supporting global projects. His team was dedicated to the Astra Zeneca/Oxford COVID-19 vaccine project where their involvement started in the early process development phase, through to delivery.
Integrity Assurance for Single-Use Systems An End-User’s Perspective
What should you consider when building an integrity control strategy for your single-use systems (SUS)? How do you overcome application challenges?
Join leading industry experts Charlotte Masy of GSK and Patrick Evrard from Pall Corporation to gain insights and answers in this webinar from BioPharma Asia on integrity Assurance for Single-Use Systems, an End-User’s Perspective. They will present several case studies to show how integrity concerns can be practically addressed for cGMP manufacturing applications and the results observed a few years on.
Attendees will learn about:
- The latest regulatory requirements for integrity assurance of SUS
- The different technologies available to control integrity of SUS
- Key parameters that affect integrity measurements
Register now for this webinar from industry experts on October 6.