IPA

Establishing Validation for an Analytical Method to Monitor Organic Impurities

Changes in the Active Pharmaceutical Ingredients (API) and drug products can cause an increase of organic impurities or the formation of new impurities. Therefore, monitoring impurities are considered a critical activity to ensure the quality of pharmaceutical products. This session will discuss different regulations that impacting the control strategies of impurities in pharmaceutical products and […]

Annual GMP Update | BPF Mise à jour Conference!

International Pharmaceutical Academy (IPA) is delighted to be hosting its 15th annual GMP Update | BPF Mise à jour on October 2-3, 2019 in the historical city of Montreal, Canada. The conference will provide attendees with insight and a plethora of information on quality, compliance, validation, and regulatory areas affecting the pharmaceutical, biopharmaceutical and allied industries. It will address compelling issues and the current challenges of GMPs in a global marketplace.