Quality by Design lies at the very heart of modern pharmaceutical development. Regulatory authorities, such as the European Medicines Agency (EMA) and the US Food and Drug Administration (FDA), are placing increasing focus on the QbD component as a part of regulatory filing. As such, QbD has become a crucial element in a streamlined drug development process. Join this University of Copenhagen Summer School to Get insight into the key principles of Quality by design (QbD) in pharmaceutical development, including quality risk management, formal experimental design, process analytical technology (PAT) and related data science.

WHAT

A 3 ECTS Continuing Professional Development course on Quality by Design in the pharmaceutical industry. Learn more and sign up HERE no later than 31st. May 2023

WHEN

14th August 2023, 09.00 to 18th August 2023 16.30

WHERE

University of Copenhagen, South Campus, Faculty of Law, Njalsgade 76, DK-2300 København S, Denmark

WHO FOR

professionals in the pharmaceutical industry, particularly in production, regulatory affairs and quality functions.