Wednesday, May 18th, 2022 at 3pm BST | 10am EDT | 4pm CEST | 7am PDT Join global industry and regulatory experts as they discuss current E&L hot topics on pharmaceuticals, biopharmaceuticals and medical devices.
Register Free: https://www.chromatographyonline.com/lcgc_w/extract_four
Join global industry and regulatory experts as they discuss current extractables and leachables (E&L) hot topics on pharmaceuticals, biopharmaceuticals and medical devices.
Extractables and leachables are an important consideration when developing medical products and devices. This conference will give you an insight into a number of different topics within the ever-changing world of E&L. This is Part 4 of a series of events covering critical issues in E&L.
Key Learning Objectives:
Who Should Attend:
Join us for these talks:
Establishing Permitted Daily Exposure (PDE) Values for Extractables & Leachables into Drug Products: Examples of Lots of Data and No Data
Allan Ader, Co-founder and Co-Managing Director of SafeBridge Consultants, Inc.
Challenges and Lessons Learned in the Study of E&L in Ophthalmic Drug Products
Christopher T. Houston, Senior Principal Scientist and Group Leader, Bausch & Lomb
Sample Enrichment Approaches for Extractable and Leachable Studies
Samuel Albeke, LC Manager at VR Analytical
Case Study: Assessment of the Leachables Risk from Change to a Small SUS Component in a Biopharmaceutical Manufacturing Process
Shane Smith, Managing Director of ExtLe Solutions Limited
Combination Products and Article 117 of the EUMDR, what you need to know
James Pink, Senior Director, Medical - Element Materials Technology
Impact of the GC-MS Injection Solvent and the Analyte Concentration on Relative Responses for Common Extractables
Gyorgy Vas, Business Technical Scientific Liaison - Intertek Pharmaceutical Services
Allan Ader, Ph.D, DABT
Co-founder and co-Managing Director
SafeBridge Consultants, Inc.
Allan Ader, PhD, DABT, is the co-founder and co-Managing Director of SafeBridge Consultants, Inc., now doing business as the SafeBridge Regulatory & Life Sciences Group, the premier resource for high level risk assessment, safety, health and environmental support to the biotechnology and pharmaceutical industry. Dr. Ader has extensive experience in performing health-based risk assessments including Permitted Daily Exposures (PDES) including evaluating toxicological and exposure information to determine potential health effects of chemicals; developing Occupational Exposure Limits and assessing compounds for toxicity and potency for compound categorization / banding and recommending handling practices and controls based on the toxicity/potency characteristics; assisting companies in testing of chemicals for their toxic effects and interpreting data from these tests; and responding to crises caused by occupational health illnesses from chemicals by assessing and evaluating risks and communicating them to employees and management. Dr. Ader has over 30 years of experience in the pharmaceutical and chemical industry including working for Syntex, Inc. in Palo Alto, California, and Olin Corporation, in New Haven, Connecticut. He received a PhD in Industrial Health (Toxicology) from the University of Michigan and an M.S. in Industrial Hygiene from Temple University. He is a Diplomate of the American Board of Toxicology.
Christopher T. Houston
Senior Principal Scientist and Group Leader
Bausch & Lomb
Chris Houston has 22 years of experience as an analytical chemist in the pharmaceutical and medical device industries. He started his career at Pharmacia & Upjohn (later Pharmacia, then Pfizer) in Kalamazoo, MI as an analytical scientist focused on chromatographic method development and extractables and leachables (E&L) in ophthalmic drug products. He joined Bausch & Lomb at the Rochester site in 2006 as head of the centralized mass spectrometry facility, becoming a founding member and eventual leader of a multidisciplinary spectroscopic structure elucidation group. During this time, he created and managed a successful E&L program for ophthalmic pharmaceuticals and served as a member of the PQRI Working Group on E&L in Parenteral and Ophthalmic Drug Products. Chris has also held roles as an E&L consultant, director of a contract analytical laboratory, and in QA. He currently leads Bausch & Lomb’s Pharmaceutical Development-Chemistry group. He holds a B.S. degree in Chemistry from the University of Michigan-Flint and a PhD in Analytical Chemistry with a Biochemistry minor from Indiana University.
Sam started his career as an R&D chemist formulating coating formulations with the same additives that he now spends his time detecting and identifying in the extractables and leachables industry. Sam has gained expertise in sample preparation to tackle chromatographically challenging matrices. He manages an exceptional team of liquid chromatographers at VR Analytical, an E&L industry leader.
ExtLe Solutions Limited
Shane Smith is the Managing Director of ExtLe (pronounced X-TEL) Solutions Limited, a company based in Cambridge in the UK. He has over 37 years of experience in industrial analytical chemistry, with three quarters of that time spent in the pharmaceutical sector. As well as being an expert on extractables and leachables (E&L), he is a specialist in trace analysis and the separation sciences.
From 2004, he worked for GlaxoSmithKline’s world class E&L team at Stevenage in the UK, managing E&L projects forglobal cross-site project teams. He was ultimately responsibility for the E&L content of successful product registrations across the world including North America, Europe, and other territories.
Shane left GlaxoSmithKline in early 2016 to pursue a career as an Independent Consultant and set up ExtLe Solutions to provide specialist consultancy services on E&L and other CMC related activities.
With well over 40 years’ combined experience dealing with E&Ls in an ever increasingly complex regulatory environment within the pharmaceutical industry, Shane and the team at ExtLe Solutions provide robust, scientifically sound E&L strategies for their clients’ products.
Senior Director, Medical
Element Materials Technology
James Pink has over 20 years of experience in the medical devices industry including 10 years as a healthcare technology expert and lead auditor for a leading European notified body.
He began his career as a product designer in the oil tools industry moving into medical physics and clinical engineering at the Royal Hallamshire Hospital in Sheffield, UK.
His industry experience includes managing product development and quality assurance programs for active and non-active implantable and combination products. James is a contributor to several medical device standards committees including ISO13485, ISO 14971 and various product-related standards.
Gyorgy Vas Ph.D.
Business Technical Scientific Liaison
Intertek Pharmaceutical Services
Gyorgy Vas has over 20 years of experience in scientific research, pharmaceutical and medical device product development, and laboratory management. More than half of this time was spent in a cGMP environment, where that scientific expertise was applied to solve problems related to finished pharmaceutical products and medical devices. In his current position, he is advising regulatory filing strategy for multiple clients, and his group provides solutions for mitigate deficiency letters.
He is serving as an internal scientific consultant to the laboratory operations, evaluating new analytical techniques, software products for extractables and leachables testing. As part of his current role he is involved to evaluate and implement non-routine analytical instrumentations and methods for cGMP use. He recently published two scientific papers for E&L testing. His papers have been cited more than 3000 times over the years.
Register Free: https://www.chromatographyonline.com/lcgc_w/extract_four