Date and time: October 21 from 10:00 to 11:15 Kyiv time
Speaker: Kim Bruggink, Ph. D. in Medical Sciences, Regulatory Affairs Consultant at Starodub B.V. (Netherlands). Nearly 10 years of experience in regulatory affairs for pharmaceutical and biological products. Specialized in CMC (IND/IMPD/MAA preparations, post-approval variations, Drug Master Files) and eCTD dossiers
Target Audience:
– Regulatory specialists in pharmaceutical or biological medical products
– Regulatory documentation developers
– Regulatory documentation publishers
The cost of connecting to the webinar for one computer (participant) is 50 USD.
VAT is not paid.
Discounted price 35 USD:
– when registering by 07.11.2024 inclusive;
– for client companies of the Conformity Assessment Body of LLC “UKRMEDCERT”.
Discounted price 25 USD:
– for each subsequent participant from the same organization.
The cost includes: information service, video recording of the webinar, a set of training materials and a certificate in pdf format.