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On October 28, the Department of Medical Device Supervision of the State Food and Drug Administration held a video report meeting on the special rectification of colored contact lenses to further unify requirements, grasp the progress of special rectification, exchange experience of special rectification, and ensure the in-depth advancement
of special rectification.
of special rectification.
At the meeting, the drug regulatory departments of ten provinces, cities and counties (districts) that are the key points of the special rectification work of color contact lenses made exchange speeches and reported the experience and practices and results of
the special rectification work.
the special rectification work.
The Jiangsu Provincial Food and Drug Administration and the Provincial Market Supervision Bureau jointly issued the "Jiangsu Province Decorative Color Contact Lens Special Rectification Work Plan" in combination with the actual situation, proposing seven work priorities
.
.
The Xinjiang Uygur Autonomous Region Food and Drug Administration has included the special rectification work in the annual drug safety assessment projects of all prefectures, compacted the responsibilities of regulatory departments at all levels, and promoted the implementation of the
work.
work.
The Market Supervision Bureau of Shenyang City, Liaoning Province highlights targeted supervision, builds a grid-based intelligent supervision mechanism for medical devices, and assigns "one enterprise, one code" identity coding to realize interactive services
such as accurate information push, online query, real-time evaluation, complaint reporting and information feedback.
such as accurate information push, online query, real-time evaluation, complaint reporting and information feedback.
The Market Supervision Bureau of Jinhua City, Zhejiang Province, carried out "experiential" unannounced visits, "meticulous" planning, and "accurate" attacks, and carried out "three-style law enforcement" to severely crack down on violations of
laws and regulations related to color contact lenses.
laws and regulations related to color contact lenses.
The Market Supervision Bureau of Hefei City, Anhui Province, relies on the "National Medical Device Network Sales Monitoring Platform" and "Hefei Network Transaction Supervision Service Platform" to increase network monitoring efforts and order rectification of enterprises that find problems
.
.
The Guangzhou Municipal Market Supervision Bureau of Guangdong Province conducts responsibility interviews with third-party platforms for relevant medical device online transaction services, urges them to implement corporate responsibilities, and monitors
the sales behavior and information of colored contact lenses on the platform.
the sales behavior and information of colored contact lenses on the platform.
The Market Supervision Bureau of Deyang City, Sichuan Province, adopts front-end guidance, mid-end supervision, and end-end disposal to jointly promote the supervision and governance of color contact lenses, unblock the channels for complaints and reports, and accept and deal with them
in a timely manner.
in a timely manner.
The Shanghai Qingpu District Market Supervision Bureau relies on Internet big data and combines historical regulatory data to investigate and deal with business enterprises
engaged in online sales in accordance with the law.
engaged in online sales in accordance with the law.
The Market Supervision Bureau of Laoshan District, Qingdao City, Shandong Province, implements "no greeting, random selection, and surprise inspection" for enterprises, and shoots and publishes small videos of common sense for supervision and purchase on multiple platforms, so as to enhance the public's ability to identify fake and distinguish fake and their awareness of
rights protection.
rights protection.
The Market Supervision Bureau of Xinhua County, Loudi City, Hunan Province, has created a strong social atmosphere
through the "five advances" activity of publicizing the knowledge of colored contact lenses in enterprises, training into classrooms, popularizing science at the grassroots level, caring for schools, and broadcasting into rural areas.
through the "five advances" activity of publicizing the knowledge of colored contact lenses in enterprises, training into classrooms, popularizing science at the grassroots level, caring for schools, and broadcasting into rural areas.
The meeting pointed out that the investigation and handling of cases is a key task
in the current special rectification work.
Drug regulatory departments at all levels should continue to increase the intensity of investigation and handling of illegal production and operation of colored contact lenses, accelerate the verification of network monitoring leads and the investigation and handling of complaints and reports, carry out case investigation and handling work strictly, seriously and quickly, and strictly implement regulatory responsibilities
.
in the current special rectification work.
Drug regulatory departments at all levels should continue to increase the intensity of investigation and handling of illegal production and operation of colored contact lenses, accelerate the verification of network monitoring leads and the investigation and handling of complaints and reports, carry out case investigation and handling work strictly, seriously and quickly, and strictly implement regulatory responsibilities
.
The meeting emphasized that the investigation and governance of medical device quality and safety risks is the key work
of medical device supervision this year.
In the special rectification of colored contact lenses, drug regulatory departments at all levels should urge enterprises to seriously conduct self-inspection, implement the main responsibility, and strictly regulate production, operation and online sales
.
It is necessary to sort out and investigate potential risks in a timely manner, organize risk consultations, study risk prevention and control measures, establish risk lists and implement sales number management, and effectively eliminate potential risks
.
At the same time, set up examples, play a leading role in demonstration, and promote the standardized development of
color contact lens production and management enterprises.
of medical device supervision this year.
In the special rectification of colored contact lenses, drug regulatory departments at all levels should urge enterprises to seriously conduct self-inspection, implement the main responsibility, and strictly regulate production, operation and online sales
.
It is necessary to sort out and investigate potential risks in a timely manner, organize risk consultations, study risk prevention and control measures, establish risk lists and implement sales number management, and effectively eliminate potential risks
.
At the same time, set up examples, play a leading role in demonstration, and promote the standardized development of
color contact lens production and management enterprises.
The meeting required that drug regulatory departments at all levels should work together to carry out in-depth special rectification of colored contact lenses; Strengthen regulatory coordination and linkage to ensure the formation of regulatory synergies; Unblock channels for complaints and reports, and strengthen social co-governance; Popularize the knowledge of color contact lenses and strengthen publicity and guidance
.
.
Relevant responsible persons and relevant personnel of the Device Supervision Department of the State Food and Drug Administration, the Verification Center, the Acceptance and Reporting Center attended the meeting
at the main venue.
The responsible persons and relevant personnel of the Drug Administration of all provinces, autonomous regions, municipalities directly under the Central Government and the Xinjiang Production and Construction Corps, the relevant responsible persons and relevant personnel of the Southern Institute of the State Food and Drug Administration, and the relevant responsible persons and relevant personnel of the market supervision bureaus of some cities, districts and counties attended the meeting
at the branch venues.
at the main venue.
The responsible persons and relevant personnel of the Drug Administration of all provinces, autonomous regions, municipalities directly under the Central Government and the Xinjiang Production and Construction Corps, the relevant responsible persons and relevant personnel of the Southern Institute of the State Food and Drug Administration, and the relevant responsible persons and relevant personnel of the market supervision bureaus of some cities, districts and counties attended the meeting
at the branch venues.
