Live Q&A – Extractables and Leachables Assessment of Cell and Gene Therapies
extractables and leachables assessment of Cell and Gene Therapies
Join us for a live Q&A session focused on extractables and leachables assessment of cell and gene therapies (C>s). To get the conversation started, we recently released an article to describe how and why E&L in cell and gene therapies are important, and another article comparing C> with mAb. As we get closer to the event, we will release a further article.
For more information on the event, download the pdf. Want to join in? Then register below.
Jason Creasey, Managing Director, Maven E&L Ltd
Jason Creasey is a graduate Analytical Chemist. He set up in 2019 as Maven E&L Ltd providing advice on the topic of extractables and leachables, after working for GSK in this area since the mid-1990s. Before setting up Maven E&L Ltd he was the director of a team of analytical chemists who were responsible for GSK’s global R&D support for E&L activities across a wide range of product types and modalities. He has had the pleasure of commenting on OINDP PQRI guidelines on E&L for GSK and co-authoring a chapter within a book entitled “Leachables and Extractables Handbook: Safety Evaluation, Qualification, and Best Practices Applied to Inhalation Drug Products”.
Sara Ullsten, R&D Section Manager, Cytiva
Sara Ullsten is R&D Section Manager at Cytiva. She manages the extractables and leachables lab, focused on testing polymeric materials and components used in the manufacturing of biopharmaceutical drug substances and products. She has 15 years of experience in the Life Sciences’ field and has held several positions in R&D as a senior scientist, project manager, and section manager. Sara has a Doctors’ degree in chemistry from Uppsala University.
Noemí Dorival-García, Research Fellow at NIBRT
Noemí holds a Ph.D. in Analytical Chemistry from the University of Granada, focusing on the development of analytical methods for the determination of pharmaceuticals, endocrine disruptors and emerging contaminants in environmental and biological matrices. She has held various positions focusing on E&L at institutes such as NIBRT and Enterprise Ireland (in collaboration with Janssen Sciences Ireland). She was also awarded with a research grant to lead another Project about “Assessing Effects of Leachables and the Quality of Single-Use Systems in Cell and Gene Therapy Manufacturing”.
Nick Morley, Principal Scientist, Hall Analytical
Nick has over 12 years of experience in the field of extractables and leachables, both in large pharma and at a CRO. He is responsible for providing technical/consultative support to new and existing customers in the field of E&L. Experience working on a range of products including pharmaceutical/biopharmaceutical (inhalation, topical and parenteral), medical device and nicotine delivery systems.
Nick has a BSc in Chemistry, is a BSI Committee member and British representative on the CEN (European standards Committee) working group for extractables and leachables of Electronic Cigarettes & E-liquids.
Andrew Feilden, European E&L Strategic Director, Hall Analytical
Dr Andrew Feilden is the European E&L Strategic Director at
Hall Analytical. He joined Hall in November 2019 where he is a technical expert in the field of E&L testing undertaking commercial, operational and technical thought leadership activities. He has presented on the field of extractables and leachables in over 16 countries world wide. Andrew has written a number of papers and publications and is the inventor of 2 patents. He has a degree and D Phil from the University of York, is a Fellow of the Royal Society of Chemistry and was a Scientific advisor to IPAC-RS and ex-cochair of ELSIE.