Quality Risk Mangement (QRM) in Pharma
Quality Risk Management (QRM) applies throughout the life cycle of a product, from development to discontinuation. QRM is a systematic process of analyzing, evaluating, controlling and reviewing of risk factors that may compromise the quality of a medicinal product and thus patient safety. Applying QRM requires besides experience the knowledge of the various methodologies.
During this virtual classrom training the presenters will share the most important elements of Quality Risk Management.
If you are interested to register for the workshop, please contact us at firstname.lastname@example.org.
Please indicate whether you are interested to register for an individual use or for a team.
- Quality risk management in pharma
- ICH Q9
- Methodologies used for risk anaysis
- SOP for QRM – example
Dr. Lothar Hartmann & Dr. Barbara Jentges, Managing Directors of Phact GmbH.
This workshop addresses experts from Quality, Production, Development and Registration departments that are in need to apply risk tools in their daily business.
half day (4 hours)
The course material will be provided to the participants at the beginning of the training.
CHF 450,00 excl. VAT (CHF 486,45 incl. VAT)
Each participant will receive a certificate of participation at the end of the training.