16–17 January 2018 | Course | Reading, UK
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.
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.
The module is essential for all candidates who expect to take the QP Viva.
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.
RSSL's courses are flexible, cost effective and approved by the Royal Society of Chemistry.
Event venue: Reading Enterprise Centre
Tel: +44 (0)118 918 4076