Health physiotherapy group standard

China Medical Device Industry Association (CAMDI) was established in 199 1 and is an independent legal person registered in the Ministry of Civil Affairs. It is an industrial and non-profit social organization voluntarily established by units or individuals engaged in the production, management, scientific research and development, product testing and education and training of medical devices nationwide. The competent department is the State-owned Assets Supervision and Administration Commission of the State Council, which is managed by the China Federation of Industrial Economics and receives business guidance from the Ministry of Civil Affairs, the State Food and Drug Administration and other relevant departments.

At present, China Medical Device Industry Association has 17 branches and professional committees, with more than 4,000 directly affiliated members, branch members, professional members and local association members.

The purpose of China Medical Device Industry Association is to represent the interests of member units, safeguard the legitimate rights and interests of member units, continuously improve the safety and effectiveness of medical devices, and promote the healthy development of China's medical device industry.

The main work of the association

1. Reflect the reasonable demands of members to all walks of life, safeguard the legitimate rights and interests of members, and strive to eliminate industries that have an impact on them.

Obstacles to development;

2 to carry out investigation and study on the development of medical device industry, and provide policy and legislative suggestions to relevant government departments.

Opinions and suggestions on the law;

3. Organize to formulate and supervise the implementation of industrial policies, standardize enterprise behavior, actively participate in the construction of a harmonious society, and gradually

Establish a credit system to serve the people fairly and promote the healthy development of the industry;

4 to participate in the formulation, revision, publicity and promotion of national standards, industry standards and quality specifications, and to carry out the industry.

Qualification management;

5. Accept the entrustment of government departments, participate in the formulation of industry planning, and introduce major technological transformation and technology in the industry.

Preliminary demonstration of investment and development projects. Accept other tasks authorized and entrusted by government departments;

6. Organize economic and technological exchanges and cooperation at home and abroad, and coordinate domestic enterprises to participate in international market competition;

7. Carry out registration consultation and agency for three types of products and imported products, and carry out relevant certification, recognition and consultation.

Consulting work, acting as an agent to declare the export certificate of medical device products;

8. Organize relevant laws and regulations, quality, technology and vocational training of medical device industry;

9. Organize the identification and promotion of scientific and technological achievements and products in the industry, and participate in intellectual property protection and assistance meetings.

Member enterprises apply for patents according to law, and strive for relevant scientific research support and project funds for member units;

10. Conduct industry statistics, establish publications, collect, analyze and publish industry information, and conduct industry consultation;

1 1. Participate in government procurement and medical device bidding at home and abroad, and maintain fair market ranking.

Order, to provide business opportunities for legally operated member enterprises;

12. Organize exhibitions and seminars at home and abroad, and carry out activities such as attracting investment and promoting products;

13. Actively participate in industry and social welfare undertakings.