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Pharma ED – E&L/Elemental Impurities
November 13, 2018 - November 14, 2018
Ensuring Quality, Safety, and Regulatory Compliance for Drugs & Biologics
This two-day conference will examine the safety, quality, and regulatory issues involved in a wide array of contexts central to the pharmaceutical industry, including drug packaging and delivery components, single-use systems, and parenteral drug products. We will hear from key industry working groups such as PQRI and BPOG. In addition, we will focus closely on the keys to satisfying recent ICH and USP guidelines for metal impurities in current and future drug products and biologics.