On February 7, 2019, the Information Services Centre of the designated Conformity Assessment Body IMPROVE MEDICAL UA.TR.120 will conduct a Webinar concerning “Post-marketing supervision. The new requirements for medical products introduction in Ukraine”.
The event will take place at 11:00 am (Kyiv time), and Svetlana Zgonnyk, Head of the Conformity Assessment Department of IMPROVE MEDICAL, will be the speaker.
The Webinar is designed for the top-managers and representatives of medical products import companies, as well as medical products manufacturing enterprises. During the Webinar, participants will be provided with knowledge on application of the regulations for medical products. Besides that, the power of an Authorized Representative of a medical products manufacturer in Ukraine will be touched upon. In the course of a face time with the speaker, participants will have an opportunity to discuss nuances to which a medical products manufacturer should pay attention during medical products control by customs authorities in the context of market supervision.
The participation in the Webinar “Post-marketing supervision. The new requirements for the medical products introduction in Ukraine” is charge-free, but the sign up in reserve is required.
Contact person: Galina Goy, Auditor of the Conformity Assessment Body IMPROVE MEDICAL
Tel.: +38 044 355 50 30