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NSF Release New Pharma eLearning Session – Update on EU Legislation and Guidance

Published 05 July 2018

NSF International provides a comprehensive range of support services for the pharmaceutical industry covering consulting, training, auditing, remediation, quality systems and regulatory guidance on a global basis.

Providing essential CPD for the Qualified Person or Quality Professional, this interactive eLearning session will inform you about recently introduced and proposed changes to EU pharmaceutical legislation and GMP guidance. Learn at your own pace at a time convenient you.

The eLearning session covers:

  • Implementation of the Falsified Medicines Directive
  • Update on Mutual Recognition Agreement between EU and US
  • Changes to the Clinical Trial Regulation and GMP Legislation
  • GMP guidance changes for Annex 1, 13, 17, 21 and ATMP

By completing/passing this course, you will attain the certificate of completion. Once you have completed your training, the team at NSF provides additional support and guidance for any specific questions.

How to Sign Up

Register online for this session through our online learning portal.

Have a question about our eLearning? Please contact us at e-pharma@nsf.org.



Source: Company Press Release