Joint MHRA/DIA Excellence in Pharmacovigilance:
Clinical Trials and Post-Marketing

This course is designed to provide a firm grounding in key aspects of European Clinical Pre- and Post-Marketing Safety regulatory requirements. This five-day training course also includes highlights and updates on the pharmacovigilance legislation and the latest news on the international harmonisation and standardisation activities in pharmacovigilance.

CONTINUING EDUCATION
The Faculty of Pharmaceutical Medicine of the Royal Colleges of Physicians of the United Kingdom has accredited this training course with 32 CPD credits.
The Swiss Association of Pharmaceutical Professionals (SwAPP) and the Swiss Society for Pharmaceutical Medicine (SGPM) have accredited this training course with 32 credits.
DIA is an authorised training organisation accredited under the number 11 99 53383 75 to the Préfet of Ile-de-France.

What participants from previous course say:
"I found the course very enjoyable, I learned a lot and it also reinforced the knowledge I already had. The course was very thorough."
"Comprehensive overview of diverse PV topics with practical examples during a relatively short time period."
"Based on my experience I will reccomend this course to my colleagues and any one else within the industry and I am looking forward to continue to participate in DIA courses."
"This event provided a comprehensive overview of Pharmacovigilance reinforcing the linkages across the system (data collection, signal detection, risk management etc). A focused and direct way to get a broad appreciation of PV regulation as it applies today."