In 2003, Sichuan Province established the earliest provincial centralized network procurement system for pharmaceuticals, and included all medicines purchased by public hospitals in the scope of bidding.
In 2013, Sichuan Province will focus on the use of the Sunshine procurement model for high-value medical consumables.
By 2014, Sichuan Province has formed a “three-in-one†centralized procurement work pattern for pharmaceuticals, high-value medical consumables and medical equipment.
This year, before the most eye-catching Shandong vaccine incident, Sichuan Province took the lead in launching the second category of vaccine net procurement in the country.
Then, Sichuan Province proposed to build a new “five-in-one†centralized procurement model in the country, and implement centralized procurement of sunlight, medicines, high-value medical consumables, medical equipment, in vitro diagnostic reagents, and second-class vaccines.
In the “five-in-one†procurement model of the province, the procurement of sunlight for in vitro diagnostic reagents was finalized.
At present, the provincial centralized network procurement of in vitro diagnostic reagents is still blank. As the second batch of medical reform pilot provinces joined this year, Sichuan will have great reference and replication significance in this new procurement model.
Then, how will the in vitro diagnostic reagents in Sichuan Province concentrate on the procurement of nets?
On October 24th, the Sichuan Provincial Health and Family Planning Commission announced the “Measures for the Administration of Sunshine Purchasing of In Vitro Diagnostic Reagents in the Medical and Health Institutions of Sichuan Province (Consultation Draft)â€, and publicly solicited opinions from the public. The publicity time is from October 24th to November 1st, 2016.
The following is the full text of the draft for comments:
Chapter I General Provisions
The first one is to strengthen the supervision and management of the centralized procurement of in vitro diagnostic reagents in the medical and health institutions of our province, in accordance with relevant national laws and regulations and the “Implementation Plan for Sunshine Procurement of In Vitro Diagnostic Reagents in Sichuan Medical and Health Institutions†(hereinafter referred to as “ These measures are formulated in accordance with regulations such as “implementation planâ€.
Article 2 The in vitro diagnostic reagents referred to in these Measures refer to reagents, kits, calibrators, reagents, calibration materials used for in vitro detection of human samples during the prediction, prevention, diagnosis, treatment monitoring, prognosis observation and health status evaluation of diseases. Quality control products and other products. It can be used alone or in combination with instruments, appliances, equipment or systems.
Article 3 The term “concentrated net sunlight procurement†as mentioned in these Measures refers to the in vitro diagnostic reagent trading system (hereinafter referred to as “trading systemâ€) of the medical equipment procurement and supervision platform (hereinafter referred to as “medical machinery platformâ€) of medical and health institutions according to the relevant provisions of the implementation plan. ) Open online procurement and accept supervision by relevant departments.
Article 4 The medical and health institutions referred to in these Measures refer to non-profit public medical and health institutions (including the central medical institutions in Sichuan) organized by the people's governments at various levels and state-owned enterprises (including state-owned holding enterprises).
Article 5: Participating in the medical and health institutions, in vitro diagnostic reagent production and management enterprises, and the Sichuan Pharmaceutical Machinery Centralized Purchasing Service Center (hereinafter referred to as the “Provincial Drugs Centralized Purchasing Service Organizationâ€) in the province's in vitro diagnostic reagents. The parties shall abide by these Measures.
Article 6 When the State has special provisions on the procurement methods and purchase prices of in vitro diagnostic reagents, it shall be implemented in accordance with relevant state regulations.
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