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GMP Published

Chapter 2: Personnel

The correct manufacture of medicinal products relies upon people. For this reason there must be sufficient qualified personnel to carry out all the tasks which are the responsibility of the manufacturer. Individual responsibilities should be clearly understood by the individuals and recorded. All personnel should be aware of the principles of Good Manufacturing Practice that affect them and receive initial and continuing training, including hygiene instructions, relevant to their needs.

Organisations:
EMA

Version Timeline

Chronological release history

Ares(2014)968076 - 28/03/2014

Version milestone

Published

Publication Date

16 Feb 2014

Effective Date

16 Feb 2014