We are pleased to share that Vojtech Kvita, PrimeVigilance Head of Safety Reporting Unit, will be part of a panel discussion as the pharmacovigilance expert from Czech Republic at the upcoming DIA Clinical Trial Regulation Information Day for CEE Countries.
The event will be held on Tuesday, October 22nd, 8 AM – 5 PM in the Novotel Bucharest city center.
Vojtech Kvita will be part of the panel discussion session 2: “Industry Preparedness and View.”
This Clinical Trial Regulation Information Day provides a forum to prepare stakeholders from Central and Eastern European Countries for the implementation and launch of the new EU Clinical Trial Regulation (536/2014) which will replace the European Clinical Trials Directive (2001/20/EC).
For more information about the DIA Clinical Trial Regulation Information Day, please visit their website
And if you should have any questions for Vojtech or would like to discuss your needs in regards to Pharmacovigilance and Clinical Trial Regulation Information, please reach out to us at firstname.lastname@example.org
+44 (0)1483 307920
(+1) 781 703 5540
United Kingdom (Head Office)