How to check the copy of the certificate provided by the bidder?

According to the nature of the information provided by the bidder, the qualification criteria are as follows: (1) Check whether the enterprise part 3 1, business license and license 1 are consistent with the bidder's name, and whether the production (operation) period is within the validity period of bidding and purchasing, and whether it is beyond the scope of production and operation; 1.2 business license: both original and duplicate are acceptable, and the validity period of the license shall be indicated (it can be judged by the annual inspection stamp or business term); 1.3 license: subject to the valid documents provided by the bidder. During the renewal period, the enterprise shall provide the old certificate and the renewal certificate issued by the regulatory authorities. 1.4 The bidder bids in the name of the group company, but the products it provides are produced by its subordinate production enterprises, and the "two certificates" of the products it provides must be the production enterprise rather than the group company; 1.5 If the personnel, name and address are changed or merged, relevant certification materials shall be provided; 1.6 The manufacturer must have a production license; Product management and distribution enterprises must have a business license; 1.7 If a production enterprise bids for products produced by other enterprises, it must provide a copy of its business license. 2. It is required to provide a tax return 2. 1 as a scoring element for evaluating the production (operation) scale of the enterprise, otherwise the score of this bid evaluation element will be lost; 2.2 A copy of the tax return submitted must be stamped with the seal of the tax department, otherwise it will be deemed invalid; 2.3 When converting the annual sales according to the tax bill, it must be accurate. If only a certain month's tax return is provided, the actual situation will prevail, and the annual sales will not be calculated separately. 2.4 If the bidder bids in the name of the group company, but the products provided are produced by its subordinate production enterprises, the enterprise "tax return" provided by the bidder must be the production enterprise rather than the group company; 3.GSP certification 3. 1 The GSP certificate issued by the Food and Drug Administration at or above the provincial level shall prevail. 3.2 When the product manufacturer directly distributes the winning varieties, it shall obtain the sales license issued by the Food and Drug Administration of X Province in our province. 4. Letter of Commitment for Distribution If a product management enterprise distributes or a product production enterprise directly bids for distribution by itself, it shall provide the original letter of commitment for distribution. (2) The product part 1, the power of attorney issued by the product manufacturer to the product operation enterprise (the power of attorney must be in strict accordance with the format of the bidding document, and the alteration is invalid) 1. 1, and the operation enterprise must provide the original power of attorney issued by the product manufacturer or product agent when bidding; 1.2 The entrustment period of the Power of Attorney for Product Agent must be within the validity period of bidding and procurement, and the scope of authorization and the date of issuance shall be indicated, and the red seal of the production enterprise or agency enterprise shall be affixed (if the number of entrusted products is large, the attachment can be filled in); 1.3 The drugs entrusted in the product proxy must be consistent with the actual bidding products; 2. Quality Category This product centralized bidding procurement divides the bidding products with the same generic name into four quality categories: 1) Invention 4 patented products; 2) Original development products; 3) Individual quality pricing products; 4) products. The China certificate (or copy) issued or issued by the relevant state departments shall prevail. 2. 1 Invention patent products include: products with invention patent certificates or products with China protection documents of foreign invention patents (patented products within the patent protection period). 2.2 Original developed products include: 1) Original developed products refer to products that have not obtained China's invention patent certificate, invention patent protection certificate or have passed the protection period of invention patent, as well as products with original development certificate confirmed by relevant competent authorities in China; 2) It is regarded as the original developed product. 2.3 Products with independent quality pricing include: 1) imitation products with independent pricing, national quality standard drafting units and drugs with independent quality standards, domestic first imitation, quality certification of FDA or EU; 2) Other patented products and protected products without invention patents. 2.4 Other products. 3. Production standards Products participating in the bidding must provide corresponding production standards (review whether the production standards to be adopted are national standards; If it is a probation standard, whether it is within the validity period, and whether there is a confirmation application acceptance form). 4, production approval 4. 1 each production approval corresponds to a bidding product; 4.2 The product manufacturer's name must be consistent with the manufacturer applied in the approval document, production inspection report, price document and manufacturer's manual. If there is any change, relevant valid certificates must be provided; 4.3 During the review, we should pay attention to whether the production approval is valid (whether there is a cancellation record). 5. Import product registration certificate, port inspection report and validity period 5. 1 All imported products must provide import product registration certificate or import product customs clearance form within the validity period, and affix the company seal; If the import registration certificate expires and the validity period of the port production inspection report product is within the procurement cycle of this bidding drug, it shall be deemed as valid; 5.2 All imported products must provide the port inspection report of the same batch of products after 2007, and affix the seal of the unit. 6. Product Description 6. 1 Check whether there is a product name, specifications, dosage forms, etc. Consistent with the bidding varieties; 6.2 Check whether the product characteristics in the instruction are consistent with those described in the production inspection report; 6.3 Whether the manufacturer and the entrusted processing enterprise are indicated in the review instruction. 7. Price Approval 5 7. 1 For government-priced products, the price certification materials of the National Development and Reform Commission or the X provincial price department shall be submitted; 7.2 For drugs with independent pricing (market-regulated prices) and drugs with government pricing, if the National Development and Reform Commission and the X Provincial Price Bureau have not published the product prices, they must provide the certification materials issued by the production enterprises and the "Product Price Information Release Sheet" issued by the X Provincial Price Department (refer to Wan Jia Jian Han (2008) No.74); 8. The production inspection report requires the enterprise to provide a copy of the product inspection report issued by the provincial or municipal production inspection agency after June 2006; Or the 2008 production inspection report issued by the enterprise itself, all in accordance with the national quality standards, and stamped with the seal of the unit. 9. Other materials conducive to winning the bid are mainly product patent certificates, patent certificates, separate pricing documents, production process patent certificates, special packaging certificates, etc. 10. The review of product quality and reliability is based on the sampling inspection results of product quality confirmed by the real estate supervision department within two years or published on the authoritative website of the state and provided by the real estate supervision department in accordance with the provisions of the Model Document on Centralized Bidding and Centralized Bargaining (Trial). Bidders who produce counterfeit products are disqualified from bidding, and the difference between bidders who produce inferior products is evaluated. 1 1. The reliability review of product quality management assurance is based on the sampling results of drug quality confirmed by the real estate supervision department or published by the national authoritative website within two years. Evaluate and compare the differences between enterprises that once handled counterfeit new products and inferior products. Four. Qualification examination subjects and methods 1. According to the requirements of work specifications and other documents, the bidding agency is responsible for reviewing the qualification documents submitted by bidders, and submitting the audit results to the office of the leading group for centralized bidding and purchasing of products in X province for audit and filing. 2. The bidder responding to the bidding procurement activities shall submit relevant qualification documents to the bidding agency before the deadline for submitting qualification documents stipulated in the bidding documents; 3. When reviewing the qualification documents specified in the tender documents, if the tenderer thinks that the information provided by the bidder is incomplete or insufficient to provide proof, it may require the bidder to clarify. After the review deadline, all submitted documents will be invalid.