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De Vere Canary Wharf

Oct 16, 2018 8:00 AM - Oct 17, 2018 5:15 PM

1 Westferry Circus, London, E14 4HD, United Kingdom

Regulatory Aspects in Pharmacovigilance and Practical Examples

This module will provide the safety reporting requirements with case studies, the roles and responsibilities of all stakeholders of clinical trials.

Continuing Education

The Faculty of Pharmaceutical Medicine of the Royal College of Physicians of the United Kingdom has accredited this training course with 14.75 CPD credits.

The Swiss Association of Pharmaceutical Professionals (SwAPP) and the Swiss Society for Pharmaceutical Medicine (SGPM) have accredited this training course with 14.75 credits.
Special rates available for SwAPP and SGPM members.
NameCredit TypeMax CreditsCEU
Regulatory Aspects in PhV, 16-17 Oct 2018, London,Credit TypeCPDMax Credits14.75CEU0.000
Regulatory Aspects in PhV, 16-17 Oct 2018, London,Credit TypeSWAPP/SGPMMax Credits14.75CEU0.000

Statement of Credit:

All DIA training courses and meetings are accredited by the Swiss Association of Pharmaceutical Professionals (SwAPP) Commission for Professional Development (CPD) and Swiss Society of Pharmaceutical Medicine (SGPM).

This training course is accredited by the Faculty of Pharmaceutical Medicine (FPM) of the Royal College of Physicians (RCP) of the UK. Medical practitioners who are eligible for credits can click on www.fpm.org.uk/revalidationcpd/CPD/regandonlinediary for more information. If you are already a CPD member, please go directly to www.revalidation.fpm.org.uk/login to claim your credits.

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