• Facilitating contract agreements for importing medical device samples with testing laboratories and hospitals.
• Coordinating the travel of engineers and physicians for the purpose of conducting tests.
• Identifying regulatory documents applicable to medical devices and compiling information on the necessary regulatory documentation.
• Developing and revising technical and operational documentation, establishing technical specifications, and notifying changes in technical conditions.
• Implementing amendments to the registration certificate.
• Updating information in the registration dossier.
• Arranging for the issuance of duplicate registration certificates.
• Replacing the template of the registration certificate.
• Organization of conducting technical, toxicological, clinical trials, as well as trials of medical devices related to medical measuring instruments.
• Selecting interchangeable medical devices and creating comparative tables of technical characteristics.
• Drafting and formalizing requests to regulatory authorities.

Leverage our extensive expertise to ensure your medical devices meet all regulatory requirements for a successful entry into the market.