In recent years, China's medical equipment industry has been rapid development, many cities such supervision put many efforts, and also attaches great importance to the training of medical devices practitioners. In Shaoxing City Food and Drug Administration in accordance with the spirit of the "notice further decentralization and adjust the approval matters" file recently organized counties (cities, districts) Bureau directly under the branch more than 60 front-line medical equipment approval supervisory staff to carry out the examination and approval of medical devices business knowledge and training efforts to enhance the level of business of the city's system of medical devices approval of the supervising officer.
Shaoxing PUC, according to the documentation requirements of the examination and approval of the decentralization of medical devices, and medical equipment for approval of the actual operation of the on-site inspection and taught "vitro diagnostic reagents ventures of license and day-to-day supervision of the trainees," medical device enterprises administrative licensing and day-to-day supervision "and" to open a second, three types of medical equipment production license (including changes) content, provides realistic operating guide for the counties (cities, districts) Board, directly under the branch of the administrative licensing work.
Next, Shaoxing PUC will periodically stage to carry out the medical device regulatory business training, and production supervisory inspector team, through the formation of medical devices integrate regulatory resources, and improve the quality of the supervision team.
If you have any questions, please feel free to contact us.
|