After the implementation of the Medical Device Supervision Law, the Chinese medical device market has entered a standardized development era

The formal implementation of the Medical Device Supervision Law in 2019 marked a new era of development for the Chinese medical device market. The implementation of regulatory laws will help promote the standardization and development of China's medical device market, specifically manifested in the following aspects:
The product registration and approval system is stricter. The Medical Device Supervision Law clarifies the classification and review requirements for medical devices, strengthens the procedures and standards for medical device registration and approval, strengthens the review of product safety and effectiveness, and fundamentally protects the rights and interests of consumers and patients.
The quality management system of enterprises has been further improved. The Medical Device Supervision Law requires medical device enterprises to establish a quality management system and strengthen supervision and management of enterprises. This will encourage enterprises to pay more attention to product quality and safety, improve product quality and management level, and promote the development of the industry towards high-quality.

The market entry threshold is higher. The Medical Device Supervision Law stipulates behavioral norms for the production, operation, and use of medical devices, and puts forward higher requirements for market access thresholds. This will promote the development of the industry towards a healthy and standardized direction, regulate market order, improve market competitiveness and industry influence.
Market regulation is becoming stronger. The Medical Device Supervision Law has strengthened market supervision and law enforcement efforts, and has clearly prohibited and punished illegal production, operation, use, and sales. This will promote the healthy and orderly development of the market, protect the rights and interests of patients and consumers, and improve the overall image and credibility of the industry.
Overall, the implementation of the Medical Device Supervision Law will help push the Chinese medical device market into the era of standardized development, promote the healthy and orderly development of the industry, and improve the overall level of the industry. Article SourceSAKAMITI-https://www.sakamiti.com/1885.html