In order to raise the awareness of participants in the Ukrainian market of medical devices about the new requirements of the Legislation, as well as to explain to all interested parties the specifics of the application of Technical Regulations No. 753 “Medical Products”, No. 754 “Medical Products for In Vitro Diagnostics” and No. 755 “Active Medical Products for Implant ”, IMPROVE MEDICAL is actively involved in educational activities.
Our specialists conduct lectures and seminars on the following topics:
– Application of Ukrainian legislation in the field of technical regulation. Practice of application of Technical Regulations No. 753, 754, 755 dated 02.10.2013
– Certification of quality management systems according to ISO 9001 and ISO 13485 standards (for medical products and enterprises operating in the field of medical devices manufacturing).
During the seminars, participants receive not only the most complete and reliable information on the topics discussed, but also can receive qualified and competent answers to questions regarding particular cases of the application of the Technical Regulations and the functioning of the Quality Management System.
IMPROVE MEDICAL also conducts training seminars to train internal auditors to evaluate ISO 9001 and ISO 13485 quality management systems.
Lectures and seminars are conducted by certified auditors with extensive experience in assessing compliance with International Standards and Technical Regulations.
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