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Quality Risk Management (QRM) in Pharmaceutical Industry

Quality Risk Management (QRM) in Pharmaceutical Industry

2022-01-06

Quality Risk Management (QRM) is the process of identifying, evaluating, and mitigating recognized risks connected with medicines and healthcare goods. An excellent Quality Risk Management programme can be created to reduce risk to a manageable level and deliver high-quality products to protect citizens' health.





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Entry Level CMC - EU edition MasterClass

Entry Level CMC - EU edition MasterClass

12-13 December, 2022

The Entry Level CMC Masterclass covers the general requirements for small molecules and biologics.

ICH Q10: How to manage your Quality System including Quality KPIs - EU edition MasterClass

ICH Q10: How to manage your Quality System including Quality KPIs - EU edition MasterClass

12-13 December, 2022

This MasterClass is completed by fundamentals of an appropriate Quality Culture which constitute the basis for a successful PQS - besides all regulations.

Risk Management plans and its Implementation - EU edition MasterClass

Risk Management plans and its Implementation - EU edition MasterClass

12-14 December, 2022

The aim of a Risk Management plans and its Implementation Masterclass is to document the risk management system considered necessary to identify, characterise and minimise a medicinal product’s important risks. 

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