In association with

a rolling series of pharmaceutical conferences is being offered in attractive provincial locations with internationally-recognised expert speakers with wide experience in the European licensing of medicines
"Now is precisely the time to keep investing in the skills and talents of our people”
(UK Commission for Employment and Skills,
23 October 2008)
Seize the training initiative and manage your personal career in regulatory affairs or boost the regulatory competences of your staff with attendances on our courses
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Sign Up for notification of new courses.
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To see details of our next events, please click on the links below
Building your Regulatory Understanding of Variations to Marketing Authorisations Outline
Introductory Regulatory Course on Common Technical Document (CTD) Quality Module 3 Outline
CMC (Chemistry, Manufacturing and Control) Considerations for Clinical Trial (CT) and Marketing Authorisation (MA) Applications and their Variations Outline
Understanding the Regulatory Requirements for the Licensing of Generic Medicines Outline
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The two-day courses offer exceptional value and include high-quality, carefully-structured training, accommodation for one night*, one breakfast, two lunches and a conference dinner, daytime in-course refreshments and a substantial delegates manual to reinforce the learning experience
*extra night(s) bookable if required, subject to availability
For further information about any of the conferences please click on the appropriate links above or alternatively email your enquiry to admin@pharmaqmtraining.eu
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