Other Regulatory Topics Training Modules

RRG's training modules cover a number of other topics within Regulatory Affairs, such as the Common Technical Document (CTD), Market Access, Non-clinical, Paediatrics, Pharmacovigilance and Post-Approval Changes and Variations.

Training modules on other Regulatory topics include:

 

The Basic CTD Structure CTD01
CTD Modules 2.3 and 1.4.1 - The QOS and Role of the Expert CTD02
The EU CTD CTD03
Future Trends - EU FUT01
Future Trends - US FUT02
Market Access MKT01
The Non-Clinical Dossier NONCLIN01
EU Paediatric Regulation PED01
Pharmacovigilance PV01
Pharmacovigilance in teh EU and US PV02
EU Post Approval Changes PAC01
US Post Approval Changes PAC02
Regulatory Compliance PAC03
Post Approval Changes - Documentation Requirements PAC04
Practical Application of Post Approval Changes PAC05

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T: +44 (0)1276 671 166
F: +44 (0)1276 670 960
info@rrgconsultancy.com

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RRG, Innovation House
Albany Park, Camberley
Surrey. GU16 7PL

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