Approved training courses

Course description

Our course focuses on the quality systems and the Good Manufacturing Practice (GMP)/Good Clinical Practice (GCP) interface from the QP or quality leader’s perspective. More specifically, the QP’s duties and challenges in protecting trials, volunteers and patients. Led by former IMP expert inspectors, QPs and current consultants, this course adds value to QPs, auditors and those working in clinical trial supply.

Key Learning Objectives
On completion of our IMP training course delegates will know and understand:
- The new regulations and requirements for the QP
- The subjects required in the IMP element of the QP study guide
- What regulators and inspectors look for
- How to prepare for your next inspection or IMP audit
- Where to focus audits of IMP operations on behalf of a QP
- QP duties around IMPs
- IMPs, Falsified Medicines Directive (FMD) and validation

Pre-requisites

Please speak to Aimee Harding, QP Coordinator at NSF about entry requirements for both QP training and/or postgraduate qualifications.

Additional info

Training will be delivered via a combination of an instructor-led virtual classroom and self-paced learning online. Full details will be sent to you following registration.

Training provider

NSF International

Email

qppharma@nsf.org

Tel

01751 432999