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QP Module: QP Professional Roles and Duties

14 - 15 January 2020, Reading, United Kingdom


Introduction
A Qualified Person (QP) must certify that each batch of medicinal product (for human or veterinary use) complies with its Marketing Authorisation or Clinical Trial Application, GMP and certain other requirements. Their conduct overall must comply with the Code of Practice for QPs.

This course provides a comprehensive overview of the requirements of the UK Study Guide and, by using interactive questions and scenarios, shows how the Qualified Person can comply with the legal and operational requirements of the role.

Suitability

The module is essential for all candidates who expect to take the QP Viva. It forms a valuable contribution to Continuing Professional Development for those QPs who qualified some years ago.

Other managers and supervisors from within pharmaceutical manufacturing will benefit from attending this course as they will gain a thorough understanding of the relationship of the QP with their own role.

Course Cost: £1390 (+VAT)

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Venue
The Reading Science Centre

Training Suite, The Reading Science Centre, Whiteknights Campus, Pepper Lane, Reading, RG6 6LA, United Kingdom

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Organised by
As an externally accredited training organisation (IRCA, RSC), you can be confident that by choosing RSSL you will be in safe and experienced hands. Our specialist training courses for the pharmaceutical industry cover a wide range of areas such as Qualified Person, Good Manufacturing Practice, Good Distribution Practice, Responsible Person, QMS Lead Auditor and more.

Reading Scientific Services Ltd (RSSL) has been providing industry leading scientific and technical solutions for over 30 years to the global food (FMCG), pharmaceutical, healthcare and biopharmaceutical sectors.
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