by Kamile Gruduls | Jun 9, 2021 | Pharmacovigilance, Webinar
Webinar: Strategic Pharmacovigilance Activities. Scalable and Tailor-made Outsourcing Models Larger companies often limit their strategic pharmacovigilance activities outsourcing only to highly manual and repetitive tasks, while the smaller ones may want to outsource...
by Nick | Jun 9, 2021 | Regulatory Affairs, Webinar
Webinar: Medical Device Registration in the Eurasian Economic Union (EAEU) The webinar on Medical Device Registration in the Eurasian Economic Union (EAEU) reviews the practical aspects of the approval procedure. We will discuss the various stages of the registration...
by Nick | May 25, 2021 | Regulatory Affairs, Webinar
Webinar: Affiliate Based Outsourcing for Regulatory Affairs Affiliate based Outsourcing Model for Regulatory Affairs works as a replacement or an extension of the company’s internal and local RA resources. Many challenges come up from managing your RA activities as...
by Nick | Apr 2, 2021 | Regulatory Affairs, Webinar
Webinar: Successful Medical Device Registration in EAEU: New Legislation (Part 1) The webinar discusses and explains the basic, essential, and theoretical matters of the EAEU system, outlines the new approach to the quality, safety, and efficacy assessments, and...
by Kamile Gruduls | Mar 23, 2021 | EAEU, Regulatory Affairs, Webinar
Webinar: Regulatory Strategy in the EAEU and Rest of CIS Countries Regulatory strategy in EAEU and CIS regions differ from other regions as market access to these countries can be a real challenge due to various local regulations. However, it is only a matter of...
by Kamile Gruduls | Mar 20, 2021 | Regulatory Affairs, Webinar
Webinar: Effective IMPD Writing. The Quality Part Effective IMPD writing, including the quality part is a vital document that contains information about an investigational medicinal product and it is an essential part of the Clinical Trial Application (CTA), which is...
