High-risk class of medical devices due to the special nature of the product, the product performance requirements higher, higher regulatory requirements, to ensure orderly market order Muping District Food and Drug Administration has taken a series of measures this year, will strive to improve the current situation and existing the problem, and further strengthen the high-risk medical device regulation, so this year, there are very few medical devices are safe and accident, and achieved good results.
Strengthen the supervision of medical institutions to use the devices. Diagnostic statistics on the use of units in the area of high-risk types of medical devices, purchase, storage, sale, use, supervision and improve procurement, acceptance, out of storage, registration, use the operating process to guard against the inflow of illegal channels equipment.
Strengthen practitioners business knowledge training. Take face-to-face training, a variety of ways to strengthen the will to train, organizational discussion of the training and education of the medical equipment business use units practitioners to improve the quality and safety awareness.
Comprehensively promote the construction of enterprise credit system. Advocate of industry self-regulation, to carry out themedical equipment business enterprise credit rating, the establishment of corporate credit file, and urge enterprises to establish honest and law-abiding business philosophy, consciously regulate practitioners behavior, with mechanical protection of public security.
If you have any questions, please feel free to contact us.
没有评论:
发表评论