Quality assurance agreement 1
Party A (supplier):
Party B (Buyer):
It is the obligation and responsibility of both parties to strengthen drug quality management and ensure the safety and effectiveness of drugs. In accordance with the requirements of laws and regulations such as the Drug Administration Law of People's Republic of China (PRC), the Quality Management Standard for Pharmaceutical Trading (new GSP), and on the principle of equality and cooperation, Party A and Party B sign this agreement:
1. Party A and Party B must be domestic legal pharmaceutical trading or manufacturing enterprises, and provide each other with legal, authentic and valid copies of licenses and related materials, and affix the original seals of the enterprises. If Party B's drug license and information are incomplete or invalid, the other party shall bear all economic losses and legal responsibilities of the other party. At the same time, Party A shall also provide the original Power of Attorney for Pharmaceutical Sales Personnel signed or sealed by the enterprise legal person (the name of the authorized person, ID number, authorized sales variety, region and time limit shall be stated) and a copy of the ID card, and Party B shall be responsible for the losses caused by the sales personnel conducting business without the authorization of the company.
2. Party A guarantees that the drugs provided to Party B are drugs with complete qualification information and meet the national drug production (or business) quality standards, and each batch of drugs shall be accompanied by the manufacturer's inspection report and certificate of conformity (domestic drugs) of the same batch number. When Party B purchases imported drugs from Party A, Party A shall provide copies of the Registration Certificate of Imported Drugs and the Inspection Report of Imported Drugs within the validity period of the drugs and affix the fresh seal of the enterprise.
Three. The drug packaging provided by Party A shall meet the drug quality requirements, and the packaging, labels and instructions shall conform to the regulations. Party A shall transport the drugs in strict accordance with the packaging labels, and shall meet the requirements of the drugs transported by the state when they arrive at Party B to ensure the quality of the drugs. After receiving the goods, Party B shall immediately carry out acceptance according to relevant standards. In case of shortage or damage, Party A shall be informed in time, and both parties shall actively cooperate to solve related problems in time. After Party B's acceptance and warehousing, Party B shall be responsible for the drug quality problems caused by unqualified storage conditions.
Four. If Party B finds that the varieties, specifications and quality are not in conformity with the provisions of the contract when accepting the quality of drugs, Party A shall be responsible for returning them.
5. Party A shall issue an invoice to Party B according to national regulations. If it cannot be fully listed on the invoice, a list of goods sold or taxable services provided shall be attached, stamped with the original seal of the special invoice seal of Party A, and the tax invoice number shall be indicated.
6. If consumers complain about drug quality problems, Party A shall actively cooperate with them to solve them properly. The award of drug quality problems shall be based on the appraisal report issued by the drug inspection institute at or above the provincial level, and the economic and legal responsibilities caused by the drug quality problems provided by Party A (with the provincial appraisal certificate) are true; Party A shall bear all responsibilities. If the drugs are damaged or poorly kept due to Party A's responsibility, Party B shall bear all the responsibilities.
7. When dealing with drugs provided by Party A, Party B shall contact Party A in time if it involves drug quality problems, and Party A shall provide detailed information that meets the quality standards. If both parties disagree, the inspection report of the local provincial drug inspection institute shall prevail.
Eight, the state requires the management department to adjust the relevant drug policies, involving drugs supplied by Party A, and Party A is responsible for changing (returning) drugs.
Nine. This agreement is made in duplicate, each party holds one copy, which has the same legal effect. Matters not covered herein shall be implemented in accordance with the provisions of the Drug Administration Law and the Standard for Drug Quality Management (new GSP). It shall be settled by both parties through consultation.
The validity period of this agreement: from the date of the month to the date of the month.
Party A (seal): Party B (seal):
Representative (signature) Representative (signature):
Date of signature: year month date of signature: year month day.
Quality assurance agreement 2
1, use:
In order to clarify the quality requirements of the company (hereinafter referred to as Party A) for suppliers, and serve as the basis for the supplier (hereinafter referred to as Party B) to handle and claim for compensation when the products are unqualified.
2, quality requirements:
2. 1. The performance of products provided by Party B for Party A must meet Party A's technical standards for raw materials or internal control standards for outsourced parts.
2.2. Every time Party B delivers the goods, it must provide materials such as certificate of conformity or self-inspection report to prove that the goods are qualified.
2.3. Party B's product packaging must meet the requirements of Party A; The date of production, batch number, expiration date, weight, etc. must be indicated on the package.
2.4 When Party A's customers need to go to Party B for verification, Party B shall make arrangements and cooperate with the verification.
2.5. Party B must guarantee the timely delivery capacity of 100%.
3, unqualified processing:
3. 1. If Party A verifies that raw materials or purchased parts do not meet the technical standards of raw materials or internal control standards of purchased parts, Party B must return them, and Party B shall bear Party A's transportation expenses and testing expenses. (transportation fee per100kg; 10 yuan/10 km, and the inspection fee is 30 yuan/100 kg).
3.2. If Party B's materials are found to be unqualified, Party B shall make timely rectification according to the information provided by Party A, and submit a report on rectification measures to Party A within 15 days, and the goods can be delivered again after being confirmed by Party A. ..
Remarks: (Although our company conducts performance tests or inspections on key materials, important materials and general materials, Party B cannot shirk its responsibilities and bear all losses if there are quality problems during use).
Signature (Seal) of the person in charge of Party B: Signature (Seal) of the Quality Assurance Department:
Quality Assurance Agreement 3
Party A: (supplier)
Legal representative:
Domicile:
Party B: (Buyer) Shenzhen Yitong Pharmaceutical Co., Ltd.
Legal Representative: Shi
Address: Consistent Pharmaceutical Building, No.0/5, Bagua 4th Road, Futian District, Shenzhen.
In order to ensure the quality of drugs and maintain the corporate image, Party A and Party B signed the following drug quality assurance agreement through consultation based on the principles of reasonable, fair and just purchase and sale, and in accordance with laws and regulations such as the Drug Administration Law of China and the Product Quality Law of China:
1. Party A is responsible for providing Party B with copies of its legal (pharmaceutical production (business) license) and business license and gsp(gmp) certificate, and affixing the original seal.
2. If Party A supplies Party B for the first time or the sales staff of Party A changes, Party A shall provide Party B with the original Power of Attorney and a copy of the ID card of the pharmaceutical sales staff, which shall be signed by the legal representative of the company.
3. Party A shall provide Party B with qualified drugs that meet the quality standards. The packaging, labels and instructions of drugs should comply with the relevant provisions of the state and industry, and packaging can ensure the quality of goods and the requirements of commodity transportation. And in the process of transportation, it is carried out in strict accordance with the packaging label to ensure the quality of drugs.
Four. All drugs supplied by Party A must be accompanied by drug certificates.
5. When supplying drugs, Party A shall provide corresponding production approval documents, quality standards and ex-factory inspection reports. When Party A supplies imported drugs, it shall provide a copy of the (imported drug registration certificate) and the same batch number (imported drug inspection report). Imported blood products should provide a copy (biological products import approval) and the same batch number (imported drug inspection report). For drugs produced by enterprises in Hongkong, Macau and Taiwan Province Province, China, a copy of (pharmaceutical product registration certificate) and the same batch number (imported drug inspection report) shall be provided. The above approval documents shall be stamped with the original seal of Party A's quality management organization.
The Chinese herbal medicines provided by intransitive verb A to Party B shall be marked with the name, place of origin, supplier and factory date, the Chinese herbal pieces shall be marked with the name, manufacturer and production date, and the varieties of Chinese herbal medicines and Chinese herbal pieces subject to the approval number management shall also be marked with the approval number.
7. Party A shall be responsible for all losses caused to Party B by quality problems (including packaging quality) of drugs provided by Party A. In case of any dispute between the two parties on the quality of drugs, the inspection report of the statutory inspection department shall prevail.
Eight. If Party B finds any quality problems when dealing in the drugs provided by Party A, it shall promptly notify Party A and provide detailed and clear quality information. Cooperate with Party A in investigation and evidence collection and after-treatment work.
9. When Party B purchases drugs from Party A, it shall provide Party A with a legal and effective enterprise qualification certificate (a copy of the license, with the original seal of Party B).
X. In the process of sales, if the batch number of drugs is outdated or unsalable due to market reasons, Party A promises to return it. During the execution of the valid agreement, the validity period of unsold drugs of Party B is within three months (including three months). At the urging of Party B (Party B notifies Party A by ems express mail and sends it to Party A's residence address), Party A has the obligation to dispose of the surplus stock, and the losses caused thereby shall be borne by Party A. If the validity period of the drug is less than one month (including one month) and Party A fails to dispose of it, Party B shall handle it by itself, and all losses shall be borne by Party A..
XI。 Party A shall deliver the goods by railway or entrusted transportation company; Party A shall be responsible for all losses or damages caused by drugs during transportation.
12. The terms involved in this agreement shall be discussed by both parties on the premise of not violating the mandatory provisions of laws and regulations.
Thirteen. The place of performance of this Agreement is Shenzhen, Guangdong; If there is any dispute in this agreement, bring a lawsuit to the court where the agreement is performed.
Fourteen The above terms are confirmed by both parties. Matters not covered in this agreement shall be settled by both parties through consultation.
15. This agreement is made in duplicate, with each party holding one copy, which shall take effect from the date of signing and be valid for one year.
Party a: party b: Shenzhen uni-president pharmaceutical co., ltd.
(Seal) (Seal)
Representative: representative:
Date of signature: year month date of signature: year month day.
Quality Assurance Agreement 4
Party A: _ _ _ _ _ _ _
Party B: _ _ _ _ _ _
In order to implement the good manufacturing practice, define the quality responsibility and ensure the safety and effectiveness of drugs, Party A and Party B have reached the following quality assurance agreement through consultation.
(I) Obligations of Party A:
1. Party A shall provide Party B with copies of the Pharmaceutical Production (Trading) License and Business License, and affix the official seal (red seal) of Party A. ..
2. The drugs sold by Party A must meet the following requirements:
1, which meets the legal quality standards;
2, should have a legal approval number and production batch number; (Exceptions stipulated by the State)
3, packaging identification in accordance with the relevant provisions and storage requirements;
4, generally should be issued within three months of drugs, and attach a certificate, the first business varieties must be attached to the factory inspection report;
5. The batch number of each batch of the same variety shall not exceed 10, and shall not exceed 2 batch numbers within 1 00;
6, Chinese herbal medicines should indicate the origin.
Three. When Party A provides imported drugs, it must affix the red seal of Party A's quality management organization to the inspection report and the copy of the Import Drug Registration Certificate of the port drug inspection office of this batch number, and the copies should be legible.
4. Party A shall take full responsibility for the drugs provided. If the drug quality is unqualified, it shall bear all expenses such as inspection fees, confiscation of fines and disposal.
(II) Obligations of Party B:
1. Party B shall also provide Party A with copies of the Pharmaceutical Trading Enterprise License and Business License, and affix the official seal (red seal) of Party B. ..
(3) Description of the agreement:
1. This agreement is applicable to written purchase contracts and purchase contracts that are not established in written form.
2. This Agreement is made in duplicate, with each party holding one copy.
Three. This agreement shall be valid for three years from the date of signing by both parties.
Four. Matters not covered in this agreement shall be settled by both parties through consultation.
Party A (seal): _ _ _ _ Party B (seal): _ _ _ _ _ _
Representative (signature): _ _ _ _ Representative (signature): _ _ _ _ _ _
_ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _
Quality assurance agreement 5
Party A: (hereinafter referred to as Party A) Party B: (hereinafter referred to as Party B)
1, use
Ensure the effective operation of Party A's quality and system; In order to ensure the stability of Party B's supply quality, meet the final product demand of Party A's users and prevent the occurrence of unqualified products, this agreement is specially signed.
2. Scope of adaptation
This agreement is applicable to Party B who provides Party A's products.
3. Contents involved in the contract between the two parties
3. 1 The contract order sent by Party A to Party B shall be accurately marked with: product name, model specification, delivery date, delivery method and quality guarantee period.
3.2 If Party A needs to change the contents of the contract (order) that has been issued but has not been executed, it must notify Party B in writing, and Party B shall confirm and correct the contents of the contract (order) to Party A's representative in time.
3.3 The contract order sent by Party A to Party B shall be accompanied by the quality and technical indicators and requirements of the processed and purchased products. If Party A can't clearly put forward the quality and technical indicators, it can adopt national standards or be put forward by Party B on its behalf, and a written record will be formed after both parties agree.
4. Description of quality standards
4. 1 Party A shall explain the product quality standards to Party B through drawings, standards or designated samples.
4.2 If there is any objection to the quality standard proposed by Party A, or Party B requests to change it, Party B shall apply to Party A for negotiation.
4.3 Qualified rate of products provided by Party B to Party A:
The product quality is not less than%, and the quality guarantee period is years.
The product quality is not less than%, and the quality guarantee period is years.
The product quality is not less than%, and the quality guarantee period is years.
The product quality is not less than%, and the quality guarantee period is years.
5. Quality inspection and confirmation
5. 1 Party B shall issue the factory inspection report of each batch of Party B's products according to the quality standards agreed by both parties. If necessary, Party B shall submit quality certification materials such as inspection benchmark and QC engineering list of Party B's products to Party A for confirmation.
5.2 Quality inspection is carried out at the initial stage of supply, and it is also carried out at ordinary times.
5.3 If Party A or Party B cannot complete the agreed project or national compulsory inspection, it must be carried out in the national inspection institution designated by the quality management department of Party A, and the inspection expenses shall be borne by Party B. ..
5.4 When Party A deems it necessary, Party A may inspect accessories or supervise Party B's quality assurance system at any time.
5.5 When Party B changes its production site or key processes and equipment, it must notify Party A and get Party A's approval.
6. Party B's liability for compensation
When the matching problem meets one of the following requirements, Party B shall bear the compensation liability agreed in the following 7. 1 A: The unused products of Party B do not meet the quality and technical requirements of Party A at all;
B: Party B's unilateral failure to deliver the goods on time affects the delivery time of Party A's products;
C: Problems arising from poor storage or maintenance of accessories or during transportation after inspection at the place where Party B supplies them (this clause applies to products stored and transported by Party B);
D: Sporadic unqualified products of products supplied by Party B inspected by Party A;
E: Party B's products have been accepted, and Party A found that more than 3% of Party B's products did not meet Party A's quality requirements during the production process; F: After-sales maintenance, return and transportation expenses of Party A's products caused by Party B's disqualification;
G: Other problems caused by Party A's failure to judge that Party B's ex-factory quality is qualified, but the actual quality does not meet the requirements; H: 1 percentage point when the qualified rate of batch products provided by Party B to Party A is less than 4.3 items;
J: When the qualified rate of batch products provided by Party B to Party A is less than 4.3 items and 2 percentage points;
K: Due to the needs of Party A's customers, after consultation with Party B, the batch pass rate is lower than the above J percentage points. ..
7. Requirements
7. 1 When Party B's products conform to the sub-items in Article 6 of this Agreement, Party B shall compensate according to the following liabilities corresponding to the sub-items in Article 6:
A: The problem is caused by product defects other than the accessories provided by Party A;
B: Problems caused by Party A changing the structure or style of accessories without consulting Party B;
C: After the products of Party A are delivered to the end users, the owners or users of the products use, keep or change the structure without authorization, resulting in problems;
D: Problems caused by defects in the technical drawings provided by Party A to Party B;
E: Problems caused by improper use and maintenance of Party A;
F: Problems caused by Party A's improper storage or maintenance.
8. Others
8. 1 This agreement is valid for one year.
8.2 This Agreement is made in duplicate, with each party holding one copy. Matters not covered herein shall be discussed separately by both parties.
(Party A) (Party B)
Signature/date of representative (seal): signature/date of representative (seal)
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