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.
The company provides essential consulting professional development (CPD) for the qualified person or quality professional, and this interactive eLearning session will inform you about recently introduced and proposed changes to EU pharmaceutical legislation and good manufacturing practice (GMP) guidance. Learn at your own pace at a time convenient for 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 Advanced Therapy Medicinal Products (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
If you are interested in signing up, make an enquiry using the form on this page or register online at nsfpharmabiotech.trainingfolks.com/store.