On February 7, 2019, a Training Webinar concerning medical products post-marketing supervision in Ukraine was conducted, what allowed participants to consider and discuss the following issues:
- Procedure of the post-marketing supervision.
- Supervision scenario.
- Complaints statement.
- Authorized representative: contract or power of attorney?
- Sectoral market supervision plan for medical products in 2019.
During the Webinar, its participants not only had an opportunity to get acquainted with the latest information on post-marketing supervision procedures, nuances of obtaining the Certificate of Conformity, on the EU Certificate recognition procedure, but also examined specific situations related to the conformity assessment procedure in Ukraine, powers and organization of the Authorized Representative activity, etc.
According to the speaker of the event, Svetlana Zgonnyk, Head of the Conformity Assessment Department of IMPROVE MEDICAL, the questions discussed at the Webinar will help market members to avoid common mistakes made during preparation to the procedure of medical products introduction and circulation.
The IMPROVE MEDICAL experts regularly inform market members about application features of the Ukrainian legislation regarding technical regulation of the medical products market. Our company is always open to dialogue and ready to provide necessary advices to all market members.
Tel.: +38 044 355 50 30