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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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Regulated LC-MS Bioanalysis Masterclass

Regulated LC-MS Bioanalysis Masterclass

26 & 27 January, 2022

This training is intended for professionals who work in the field of analytical chemistry, focusing on HPLC, UHPLC and LC-MS. This training will provide effective method development, sample analysis and comprehensive troubleshooting.

Advanced Stability Testing of Pharmaceuticals MasterClass

Advanced Stability Testing of Pharmaceuticals MasterClass

01 - 04 February, 2022

Advanced Stability Testing of Pharmaceuticals MasterClass will cover the scientific principles of chemical & physico-chemical degradation of active substances & pharmaceutical products.

Advanced E-PPI and E-Leaflet US MasterClass

Advanced E-PPI and E-Leaflet US MasterClass

07 & 08 February, 2022

This Training will provide Key Points for the Establishment, Development and Implementation of E-PPI strategy and E-Leaflets.

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