Guangdong: Taking multiple measures simultaneously to carry out the publicity and implementation activities of the newly revised "Regulations on the Supervision and Administration of Medical Devices"

Medical Network, June 1st.
Recently, the Guangdong Provincial Drug Administration held a provincial system of medical device legal backbone training courses in Dongguan.
The purpose is to train the newly revised "Regulations on the Supervision and Administration of Medical Devices" (hereinafter referred to as the "Regulations") to publicize and implement teachers and The backbone of the law makes it the backbone of the promotion and implementation of the "Regulations" at all levels in the province.
The State Food and Drug Administration strongly supported this training course.
Deputy Director Zhang Hua of the Registration Department and Director Zhao Yan of the Evaluation Center personally came to the site to teach.

 

Organize training courses for key medical equipment legal professionals across the province

 

Integrate legal requirements with business supervision

 

The newly revised "Regulations on the Supervision and Administration of Medical Devices" were promulgated by the State Council on February 9, 2021, and will come into force on June 1, 2021.
This is another major move in the field of medical device supervision in my country.

 

This medical device legal backbone training class is one of the important contents of the publicity and implementation activities, reflecting three characteristics: First, scientific authority.
The training strictly follows the legislative intent of the Regulations, accurately interprets the legislative spirit and revised content of the Regulations, insists on uniformity, accuracy, and authority, with comprehensive content and prominent themes.
The second is various forms.
In addition to specific lectures, the training also arranges examinations, so that everyone can learn with questions, improve learning initiative and pertinence, and help enhance classroom interaction and sense of participation.
The third is to be close to reality.
The training closely combines legal regulations with business supervision, business learning and teaching skills, and is highly targeted and practical.

 

　　More than 170 medical device supervisors from the market supervision bureaus of various cities and some counties (districts), relevant departments of the provincial bureau, and directly affiliated units participated in the training.

 

　　Various forms of publicity activities are organized throughout the province

 

　　In order to conscientiously publicize and implement the "Regulations", the Guangdong Drug Administration attaches great importance to it, and takes multiple measures to carry out publicity and implementation activities.
The activities that have been carried out include: organizing an overall view of the new "Regulations" organized by the National Medical Products Administration Establishing the "Regulations" law popularization group, carrying out the "Regulations" publicity and implementation work through a variety of new media, editing and printing the "Regulations" leaflets, etc.
; upcoming activities include: organizing a party group central group to conduct "Regulations" law popularization lectures, respectively for local governments Carry out "Regulations" law promotion and implementation activities with enterprises across the province, produce "Regulations" animation promotional videos, publicity panels and promotional leaflets, carry out clean-up of regulatory documents, and hold seminars on hot issues after the implementation of "Regulations".

 

　　On March 25, at the "Guangdong Province 2020 Quality Credit Class A Medical Device Manufacturing Enterprise Press Conference" hosted by the Guangdong Provincial Drug Administration and undertaken by the Guangdong Medical Device Management Association, the authoritative interpretation of the new "Regulations" was carried out.
The prelude to a series of publicity activities was opened.
Yan Zhen, deputy director of Guangdong Provincial Drug Administration, comrade in charge of the Greater Bay Area Center for Medical Device Technical Evaluation and Inspection of the State Drug Administration , comrade in charge of relevant departments of the Provincial Drug Administration, Provincial Medical Device Quality Supervision and Inspection Institute, Provincial Drug Administration review and certification Center, Institute for Drug adverse reactions monitoring Center, related to market supervision Authority and medical equipment manufacturing enterprises , trade associations on behalf of more than 350 people attended the conference.

 

　　It is understood that various publicity and implementation activities have also been organized and carried out in various parts of Guangdong province.
The Guangzhou Municipal Market Supervision Bureau held a special lecture and training meeting in the form of video conference, and invited Zhang Feng, the director of the Medical Device Division of the Provincial Drug Administration to give lectures and guidance.
The conference set up a main venue and 18 sub-venues.
More than 800 people from the city's two-level market supervision departments and technical institutions attended the conference.
Shenzhen held a legal promotion and implementation training meeting, using offline training and online live broadcast.
Wang Lanming, Commissioner of the Medical Device Registration Management Department of the State Food and Drug Administration, and Wang Xin, Director of the Second Supervision Division of the Medical Device Supervision Department of the State Food and Drug Administration , Xu Liang, deputy director of the Dawan District Center for Medical Device Technology Review and Inspection of the State Food and Drug Administration, interpreted the new version of the "Regulations" in detail for the trainees.

 

　　The market supervision bureaus in Zhuhai, Foshan, Jiangmen, Heyuan, Zhaoqing and other places have also carried out various forms of new "Regulations" publicity and implementation training, setting off a new round of enthusiasm for learning the new "Regulations.
"

　　Medical Network, June 1st.
Recently, the Guangdong Provincial Drug Administration held a provincial system of medical device legal backbone training courses in Dongguan.
The purpose is to train the newly revised "Regulations on the Supervision and Administration of Medical Devices" (hereinafter referred to as the "Regulations") to publicize and implement teachers and The backbone of the law makes it the backbone of the promotion and implementation of the "Regulations" at all levels in the province.
The State Food and Drug Administration strongly supported this training course.
Deputy Director Zhang Hua of the Registration Department and Director Zhao Yan of the Evaluation Center personally came to the site to teach.

 

　　Organize training courses for key medical equipment legal professionals across the province

 

　　Integrate legal requirements with business supervision

 

　　The newly revised "Regulations on the Supervision and Administration of Medical Devices" were promulgated by the State Council on February 9, 2021, and will come into force on June 1, 2021.
This is another major move in the field of medical device supervision in my country.

 

　　This medical device legal backbone training class is one of the important contents of the publicity and implementation activities, reflecting three characteristics: First, scientific authority.
The training strictly follows the legislative intent of the Regulations, accurately interprets the legislative spirit and revised content of the Regulations, insists on uniformity, accuracy, and authority, with comprehensive content and prominent themes.
The second is various forms.
In addition to specific lectures, the training also arranges examinations, so that everyone can learn with questions, improve learning initiative and pertinence, and help enhance classroom interaction and sense of participation.
The third is to be close to reality.
The training closely combines legal regulations with business supervision, business learning and teaching skills, and is highly targeted and practical.

 

　　More than 170 medical device supervisors from the market supervision bureaus of various cities and some counties (districts), relevant departments of the provincial bureau, and directly affiliated units participated in the training.

 

　　Various forms of publicity activities are organized throughout the province

 

　　In order to conscientiously publicize and implement the "Regulations", the Guangdong Drug Administration attaches great importance to it, and takes multiple measures to carry out publicity and implementation activities.
The activities that have been carried out include: organizing an overall view of the new "Regulations" organized by the National Medical Products Administration Establishing the "Regulations" law popularization group, carrying out the "Regulations" publicity and implementation work through a variety of new media, editing and printing the "Regulations" leaflets, etc.
; upcoming activities include: organizing a party group central group to conduct "Regulations" law popularization lectures, respectively for local governments Carry out "Regulations" law promotion and implementation activities with enterprises across the province, produce "Regulations" animation promotional videos, publicity panels and promotional leaflets, carry out clean-up of regulatory documents, and hold seminars on hot issues after the implementation of "Regulations".

 

　　On March 25, at the "Guangdong Province 2020 Quality Credit Class A Medical Device Manufacturing Enterprise Press Conference" hosted by the Guangdong Provincial Drug Administration and undertaken by the Guangdong Medical Device Management Association, the authoritative interpretation of the new "Regulations" was carried out.
The prelude to a series of publicity activities was opened.
Yan Zhen, deputy director of Guangdong Provincial Drug Administration, comrade in charge of the Greater Bay Area Center for Medical Device Technical Evaluation and Inspection of the State Drug Administration , comrade in charge of relevant departments of the Provincial Drug Administration, Provincial Medical Device Quality Supervision and Inspection Institute, Provincial Drug Administration review and certification Center, Institute for Drug adverse reactions monitoring Center, related to market supervision Authority and medical equipment manufacturing enterprises , trade associations on behalf of more than 350 people attended the conference.

 

　　It is understood that various publicity and implementation activities have also been organized and carried out in various parts of Guangdong province.
The Guangzhou Municipal Market Supervision Bureau held a special lecture and training meeting in the form of video conference, and invited Zhang Feng, the director of the Medical Device Division of the Provincial Drug Administration to give lectures and guidance.
The conference set up a main venue and 18 sub-venues.
More than 800 people from the city's two-level market supervision departments and technical institutions attended the conference.
Shenzhen held a legal promotion and implementation training meeting, using offline training and online live broadcast.
Wang Lanming, Commissioner of the Medical Device Registration Management Department of the State Food and Drug Administration, and Wang Xin, Director of the Second Supervision Division of the Medical Device Supervision Department of the State Food and Drug Administration , Xu Liang, deputy director of the Dawan District Center for Medical Device Technology Review and Inspection of the State Food and Drug Administration, interpreted the new version of the "Regulations" in detail for the trainees.

 

　　The market supervision bureaus in Zhuhai, Foshan, Jiangmen, Heyuan, Zhaoqing and other places have also carried out various forms of new "Regulations" publicity and implementation training, setting off a new round of enthusiasm for learning the new "Regulations.
"