An essential course for ensuring compliance with Regulatory Requirements which will be of particular relevance for Pharmacovigilance, Regulatory Affairs, Clinical Research/Operations, GMP, QA and Document Management Functions
27 Jun 2019
& 2 Dec 2019
GBP 699 599 *
EUR 979 839 *
USD 1,090 934 *
* When you book before 10 May
This Standard Operating Procedure (SOP) course has been specifically designed to help you develop the skills to write and produce the content of SOPs, review and implement SOPs and ensure you comply in a regulated environment. You will come away with the confidence to use process to write, update and implement SOPs which can easily be used by the end users.
Please note we are also running:
This meeting runs back-to-back with Improving Processes and CAPA (Corrective and Preventative Action) on 4 December 2018 and there is a further £100/€140 discount off when booked together.
To find out more call Customer Services on +44 (0)20 7749 4730 or e-mail firstname.lastname@example.org
Attend this programme will show you:
Dr Laura Brown MBA, BSc,PhD, is a Pharmaceutical QA and Training Consultant, Course Director for the MSc in Clinical Research, School of Pharmacy at the University of Cardiff. She has more than 20 years’ experience of quality assurance in the pharmaceutical industry and has worked for several companies, including GSKs Hoechst Marion Roussel, Farmitalia and Phoenix International. She has a particular expertise in quality assurance including risked based approaches to quality systems, data Integrity and project management in the pharmaceutical industry. She regularly writes on pharmaceutical regulatory issues including “The Planning of International Drug Development”, in the Clinical Research Manual, Euromed and the “Impact of Brexit”, RQA Journal 2017.