Model quality assurance agreement

Model Quality Assurance Agreement Party A: _ _ _ _ _ _ _ _ _ _ _ Party B: _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ Party A shall abide by the national laws and regulations on drug administration, provide Party B with a legal and valid business license and a copy of the License for Pharmaceutical Trading Enterprises, and affix the official seal of Party A. Party A's business personnel shall issue a power of attorney with the official seal of the enterprise and the seal or signature of the legal representative of the enterprise, specify the scope and validity period of authorization, and provide a copy of ID card to carry out business activities within the scope limited by the power of attorney. 2. The drugs provided by Party A are qualified drugs that meet the national drug quality standards and relevant quality requirements; The drug is accompanied by a product certificate; Drug packaging meets relevant regulations and cargo transportation requirements; When Party A provides imported drugs, it shall also provide the Registration Certificate of Imported Drugs or the Registration Certificate of Pharmaceutical Products stamped with Party A's official seal, the inspection report of imported drugs or the customs clearance form of imported drugs with the same batch number. 3. If the drugs provided by Party A are patented goods, the patent certificate stamped with Party A's official seal and the latest payment certificate shall be provided. 4. The quality responsibility of the drugs provided by Party A during delivery shall be controlled according to the relevant requirements of the National Measures for the Administration of Purchase and Sale Contracts of Pharmaceutical Commodities and the Division of Transportation Responsibilities. Party A shall be responsible for the quality problems within the validity period of drugs. 5. When Party A provides medicines, the production date shall not exceed _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ 6. Party A shall reply within _ _ _ _ _ hours after receiving the letter (telegram) from Party B requesting quality inquiry. If the time limit is exceeded, Party A shall be responsible for the consequences arising therefrom. 7. The drugs provided by Party A to Party B can be returned to Party A because there is no market. If Party B can't sell because the batch number is expired, Party A must replace the original batch number and provide the same quantity of drugs with new batch number. 8. The biological products provided by Party A belong to the varieties specified in the Measures for the Administration of Batch Issuance of Biological Products (Trial), and a copy of the batch issuance certificate of biological products stamped with Party A's official seal shall be provided. 9. If any goods provided by Party A are suspected of counterfeiting patents, Party B has the right to take measures such as withdrawing cabinets and temporarily detaining the goods suspected of counterfeiting patents. 10. Party A shall bear all legal responsibilities for patent infringement disputes arising from the goods provided by Party A. Party B's responsibility 1. As a unit dealing in drugs according to law, Party B shall provide Party A with a legal and valid copy of the enterprise qualification certificate, and affix the official seal of Party B. 2. If Party B finds shortages, damages, errors, packaging pollution and appearance quality problems, and the imported drugs do not have the Registration Certificate for Imported Drugs or the Registration Certificate for Pharmaceutical Products and the Inspection Report for Imported Drugs affixed with the official seal of Party A or the customs clearance form for imported drugs of the same batch number, Within a certain date after receiving the medicine (subject to the arrival date) (this city is _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _. Party B shall contact Party A in time in case of any doubt when handling or using the drugs provided by Party A.. If there are differences between the two parties, the drug quality inspection report issued by the competent department shall prevail. Party B shall notify Party A within _ _ _ _ _ days after receiving the drug test report, and submit the report to Party A for handling. Party B shall be responsible for the consequences caused by overdue. 4. If the drugs provided by Party A have quality problems during operation or use, Party B shall provide detailed and clear quality information and actively cooperate with Party A's investigation and evidence collection and after-treatment work. 5. Party B promises to provide the drugs supplied by Party A with storage conditions that meet the national regulations, and Party B shall be responsible for the losses caused by improper storage. 6. Party B promises that Party B will be responsible for the quality problems beyond the responsibility period of Party A in accordance with the National Measures for the Administration of Purchase and Sale Contracts of Pharmaceutical Commodities and the principle of division of transportation responsibilities; Seasonal control of antifreeze and heat-resistant varieties shall be implemented in accordance with state regulations. 7. Party B promises that it will be responsible for the expenses and losses caused by non-quality problems and unreasonable return confirmed by Party A. 8. If Party B finds that the stored drugs are about to expire, it must notify Party A in advance within _ _ _ _ months before the expiration of the drugs. Three. Both parties * * * jointly undertake the responsibilities and agreed terms of 1. Party A and Party B cooperate with each other to do a good job in market research, development and quality management. 2. Party A and Party B safeguard each other's interests. If one party breaches the contract, the other party reserves the right to appeal or seek civil compensation. 3. Other clauses _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ Other terms: This Agreement shall be valid until _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _