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GMP Published

Chapter 8: Complaints, Quality Defects and Product Recalls

In order to protect public and animal health, a system and appropriate procedures should be in place to record, assess, investigate and review complaints including potential quality defects, and if necessary, to effectively and promptly recall medicinal products for human or veterinary use and investigational medicinal products from the distribution network. Quality Risk Management principles should be applied to the investigation and assessment of quality defects and to the decision-making process in relation to product recalls corrective and preventative actions and other risk-reducing actions. Guidance in relation to these principles is provided in Chapter 1.

Organizations:
EMA

Version Timeline

Chronological release history

Ares(2014)2674297

Version milestone

Published

Publication Date

Aug 13, 2014

Effective Date

Aug 13, 2014