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Join our webinar to learn about analytical considerations associated with the standard extraction protocols recommended by both BPOG and USP.
Join our webinar to learn about analytical considerations associated with the standard extraction protocols recommended by both BPOG and USP.
This webinar will explore how to conduct effective extractables and leachables (E&L) testing on plastic process materials used during pharmaceutical and biopharmaceutical manufacturing. It will delve into the new BPOG and USP best practices and examine how best to avoid potential risks to the safety, efficacy and stability of pharmaceutical and biopharmaceutical products.
This presentation will summarize the key elements of E&L studies carried out on plastic process materials used during pharmaceutical and biopharmaceutical manufacturing. It will examine the recently published BioPhorum Operations Group’s 2020 best practices guide on extractables testing of polymeric single-use components used in biopharmaceutical manufacturing. It will also delve into the significant new chapters the US Pharmacopeia (USP) plans on publishing this May as well as analytical considerations associated with the standard extraction protocols recommended by both BPOG and USP. In addition, several case studies on E&L analyses of plastic process materials will be presented.
The webinar is aimed at:
Dr. Dujuan Lu
E&L Manager/Global Lead
Dr. Lu has a Ph.D. in analytical chemistry and is an E&L subject matter expert (SME) with vast contract lab and medical device/pharmaceutical industry experience. Dr. Lu has previously worked on over 500 E&L projects across a broad range of packaging systems.
For more information, please contact:
Josela Renardson
Global Marketing Manager
t: +44 (0) 121 541 4748
400 Broadacres Drive,
Suite 200, 2nd Floor,
Bloomfield, New Jersey, 07003,
United States