Medical Guarantee Letter 1 Dear XX:
In order to strengthen the quality management of aseptic medical device products in the process of operation, ensure the quality in the process of circulation and ensure the safety of people's lives, we guarantee that:
1. We strictly implement the Regulations on the Supervision and Administration of Medical Devices, the Measures for the Supervision and Administration of Medical Device Business Enterprises, the Measures for the Supervision and Administration of Disposable Sterile Medical Devices and relevant laws and regulations promulgated by the state, and sell and operate according to law.
Two. I provide relevant certificates of legal operation, that is, business license and medical device business license, and affix the official seal of the enterprise.
We indicate the package, specification, model, production date and expiration date of the product on the sales delivery note.
Four. The internal and external packaging of medical device products supplied by our company should be firm and clearly marked, and meet the relevant provisions of product performance and quality requirements.
in this regard
Salute!
Medical Security 2 This week, the legal representatives of xx Tumor Hospital, Huanhu Hospital, Hexi Hospital and other 29 medical institutions of all levels and types in the area under the jurisdiction of xx District successively submitted the legal practice guarantee of medical institutions to the Health Bureau of XX District, in order to put an end to illegal medical practice and further promote the fight against illegal medical practice.
It is understood that there are currently 129 medical institutions in xx District, including 2 1 municipal medical institutions and 0/08 district medical institutions. In the future, the fight against illegal medical practice will be managed by the jurisdiction, and medical institutions at all levels must accept the supervision and management of the municipal and district health administrative departments. In order to crack down on illegal medical practice, xx District began to implement the responsibility of cracking down on illegal medical practice and the commitment system of good faith in practicing according to law for all kinds of medical institutions at all levels within its jurisdiction, requiring the legal representatives of medical institutions to earnestly assume management responsibilities, resolutely correct illegal acts, do a good job in practicing their own medical institutions according to law, and accept supervision and inspection by the health administrative department.
129 medical institutions and their legal representatives solemnly promise that in their future practice activities, they will resolutely put an end to illegal medical practices such as hiring non-health technicians to practice medicine, renting out departments, illegally engaging in STD diagnosis and treatment activities, illegally using B-ultrasound to identify the sex of the fetus, and selectively terminating pregnancy operations. In the future, all medical institutions with illegal medical practice will bear corresponding legal responsibilities according to law, and relevant personnel will also be held accountable.
Applicant (seal):
date month year
Medical Security 3 This week, the legal representatives of 29 medical institutions of all levels and types, including Tianjin Cancer Hospital, Huanhu Hospital and Hexi Hospital, within the jurisdiction of Hexi District successively submitted medical institutions' commitment letters to Hexi District Health Bureau to put an end to illegal medical practice and further promote the fight against illegal medical practice.
It is understood that there are currently 29 medical institutions providing medical services to the society in Hexi District, including 2 municipal medical institutions and 08 district medical institutions. In the future, the fight against illegal medical practice will be managed by the jurisdiction, and medical institutions at all levels must accept the supervision and management of the municipal and district health administrative departments. In order to crack down on illegal medical practice, Hexi District began to implement the responsibility of cracking down on illegal medical practice and the commitment system of good faith in practicing according to law for all kinds of medical institutions at all levels within its jurisdiction, requiring the legal representatives of medical institutions to earnestly assume management responsibilities, resolutely correct illegal acts, do a good job in practicing their own medical institutions according to law, and accept supervision and inspection by the health administrative department.
Twenty-nine medical institutions and their legal representatives solemnly promised to resolutely put an end to illegal medical practices such as hiring non-health technicians to practice medicine, renting contracted departments, illegally engaging in STD diagnosis and treatment activities, illegally using B-ultrasound to identify the sex of the fetus, and selectively terminating pregnancy operations. In the future, all medical institutions with illegal medical practice will bear corresponding legal responsibilities according to law, and relevant personnel will also be held accountable.
Medical Security 4 Dear XX:
In order to ensure the quality of medical devices, maintain business reputation and stabilize the normal circulation order of medical device products, our company guarantees that:
I. Our company guarantees the product quality, and if there is any economic responsibility for the product quality problems of our company; Our company will be responsible for everything.
2. Our company provides a legal and valid license, specifying the name, specifications, origin, batch number and sales date of the goods sold for future inspection.
Three. Our company abides by business reputation and professional ethics, and promises not to cheat.
in this regard
Salute!
Medical Security 5 Party A (supplier): Beijing Zhongxing Ye Ming Medical Equipment Co., Ltd.
Party B (Buyer): XXX Hospital.
It is the responsibility and obligation of both parties to strengthen quality management and provide users with safe and effective medical devices. In order to improve social and economic benefits and establish a good corporate image, the two parties signed this agreement in accordance with the Regulations on the Supervision and Administration of Medical Devices, the Measures for the Administration of Medical Device Business License and other laws and regulations and relevant industry regulations.
1. The quality standards of medical devices provided by Party A to Party B shall conform to national standards and industry standards.
2. The packaging, identification, labels and instructions of medical devices shall comply with the relevant provisions of the state and industry.
Three. When Party B purchases medical devices for the first time, Party A shall provide Party B with complete licensing and authorization procedures for Party B's sales and filing. Party A shall be legally responsible for the authenticity and legality of the information provided by it.
Four. As a commercial enterprise, when supplying goods to Party B, Party A shall provide inspection reports or other valid certificates to Party B in batches. ..
5. After the arrival of Party A's goods, Party B shall conduct acceptance inspection according to relevant standards.
6. Party B shall have the place, personnel and conditions for storing and keeping the medical devices provided by Party A. If the medical devices have quality problems due to improper storage and maintenance by Party B, Party B shall be responsible.
Seven, the two sides disputed the quality of medical devices, the inspection results of the statutory inspection department shall prevail.
Eight. Where Party B suffers economic losses due to the quality problems of Party A's products, Party A shall be responsible.
9. If Party A exaggerates the function and efficacy of the product, resulting in disputes between Party B and users and early economic losses, Party B has the right to recover from Party A. ..
X. Party A is responsible for the after-sales service of related products.
XI。 Matters not covered in this agreement shall be settled by both parties through consultation.
Twelve. This agreement is made in duplicate, one for each party.
Thirteen. This agreement shall come into force as of the date of signature and shall be valid for one year.
Party A (seal):
20XX x month XX day
Party B (seal):
20XX x month XX day
Medical Guarantee Letter 6: Hangzhou Health Service Development Center
Haihong medicine electronic trading center co., ltd
As an enterprise producing (product name), XXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXX
According to the Procurement Document of Centralized Procurement of Medical Consumables (Phase I) 20xx-20xx in Hangzhou Medical and Health Institutions (procurement documentNo.: HZHCCG-20xx- 1), once we win the bid and sign the supply agreement according to law, our company guarantees that the production standards of the above products meet the product implementation standards; During the procurement period, ensure the timely supply of sufficient goods to the enterprise. If there is any violation, bear the liability for breach of contract according to law.
I guarantee that the quality and supply guarantee issued by my unit is true and legal, and I am willing to bear all legal responsibilities.
The validity period of this letter of guarantee is: 20XX years, x months and x days until the end of this procurement cycle.
Name of production enterprise: XXXXXXXX
Handler (signature): XXXXXXX
Contact information of the manager: XXXXXXXX
Date: XX, XX, XX (with the official seal of the manufacturer)
Medical guarantee letter 7 1. Refuse to accept "red envelopes" and items presented by patients and relatives and friends. If it is difficult to refuse the money and goods offered by the patient at that time, it shall be handed over to the designated department of the unit for handling within 24 hours.
2. Refusing to accept kickbacks, commissions and other illegitimate interests from medical devices, disposable sanitary materials, medicines, reagents and other production and sales enterprises or sales agents in various names and forms. If the enterprise or salesman is found to have the above behavior, immediately notify the relevant departments.
3, introduce patients to other units for examination, treatment, purchase of drugs, or introduce others to buy medical equipment, medical devices, etc. Refuse to accept kickbacks or commissions.
4, prescription, instrument inspection, laboratory inspection and other medical examination, etc. , refused to charge commission for invoicing.
5, according to the patient's condition, standardize the prescription, reasonable inspection, don't open a big prescription, don't do unnecessary inspection.
6, polite reception, civilized service, enthusiastic service, kind attitude, don't shuffle, reprimand, make things difficult for patients.
7, the implementation of medical publicity, price and fee publicity system, respect for patients' right to choose, know and supervise.
8, the implementation of patient hospitalization "one-day list system", do not break down the fees, do not exceed the standard fees, do not charge for independent projects.
20XX x month XX day
Medical authorization 8 is to ensure the quality, safety and effectiveness of medical devices. In accordance with the Regulations on the Supervision and Administration of Medical Devices and relevant laws and regulations, strictly abide by all laws and regulations, ensure the effectiveness of product distribution operation procedures, and make the following commitments to you on the quality of medical devices sold:
1. The medical devices sold by our company include medical device business license and medical device product registration certificate;
2. The medical devices we provide meet the quality standards and are all qualified products;
3. All medical devices we provide provide standardized after-sales service;
4. Once the product quality problems are found, we will inform you in time and take corresponding measures such as recall to ensure the interests and safety of users.
This quality guarantee is valid for a long time.
Xxxxxxxx medical equipment co., ltd
Xx，xx，XX，XX
Medical Security 9 This week, the legal representatives of Tianjin Cancer Hospital, Huanhu Hospital, Hexi Hospital and other 129 medical institutions at all levels in Hexi District successively submitted medical institution commitment letters to Hexi District Health Bureau to prevent illegal medical practice and further promote the fight against illegal medical practice.
It is understood that there are currently 129 medical institutions in Hexi District, including 2 1 municipal medical institutions and 0/08 district medical institutions. In the future, the fight against illegal medical practice will be managed by the jurisdiction, and medical institutions at all levels must accept the supervision and management of the municipal and district health administrative departments. In order to crack down on illegal medical practice, Hexi District began to implement the responsibility of cracking down on illegal medical practice and the commitment system of good faith in practicing according to law for all kinds of medical institutions at all levels within its jurisdiction, requiring the legal representatives of medical institutions to earnestly assume management responsibilities, resolutely correct illegal acts, do a good job in practicing their own medical institutions according to law, and accept supervision and inspection by the health administrative department.
129 medical institutions and their legal representatives solemnly promise that in their future practice activities, they will resolutely put an end to illegal medical practices such as hiring non-health technicians to practice medicine, renting out departments, illegally engaging in STD diagnosis and treatment activities, illegally using B-ultrasound to identify the sex of the fetus, and selectively terminating pregnancy operations. In the future, all medical institutions with illegal medical practice will bear corresponding legal responsibilities according to law, and relevant personnel will also be held accountable.
Medical Guarantee 10 In order to strengthen the quality management of medical devices, ensure the quality of devices, safeguard the interests of both parties and safeguard the rights and interests of consumers, Party A and Party B sign the following quality guarantee agreement on the principle of equal cooperation:
1. Party A and Party B must be legal business enterprises with complete licenses, that is, they have the necessary licenses such as Pharmaceutical Device Business License, Business License and Medical Device Registration Certificate. Party A must provide the power of attorney of the legal person, the entrustment period and a copy of the ID card of the equipment purchase and sale personnel for Party B's record.
2. The supplier shall ensure that the quality of operating equipment meets the national equipment standard (is0 13485). The inner, outer packaging and instructions of commodities must comply with the relevant provisions of the state.
3. The product packaging provided by Party A to Party B must meet the quality requirements of medical devices, and the packaging must be firm and meet the requirements of storage and transportation. The storage and transportation conditions of Party B shall meet the requirements of medical devices. After the goods are delivered, Party B shall be responsible for the economic losses caused by improper storage and transportation.
4. After receiving the goods shipped by Party A, Party B shall timely check and accept them, and notify Party A to deal with them in time if the goods are found to be lost or damaged.
5. If the medical devices 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, evidence collection and after-treatment work.
Matters not covered in the above clauses of intransitive verbs shall be determined by both parties through consultation.
Seven. This agreement shall come into effect after being confirmed and sealed by both parties.
Eight. This agreement is made in duplicate, one for each party.
Nine. The validity of this agreement: xx, xx, xx, XX.
Party A (seal): xxx
Party B (seal): xxx
Xx，xx，XX，XX
Medical guarantee 1 1 name: XX gender: XX date of birth: XX year XX month home address: XX ID number:
This comrade handled the medical insurance relationship in XX company in XX. According to the provisions of the Measures for the Administration of Social Security Funds, a person can only have one social security relationship. Please "new rural cooperative medical care" management department to stop the "new rural cooperative medical care" relationship.
Hereby certify that
XX Company (with official seal)
XX year XX month XX day
Medical insurance 12 I am a college student. Through the publicity of the school, on the basis of a comprehensive understanding of college students' participation in urban residents' medical insurance and relevant policies of the school, I voluntarily refused to participate in the basic medical insurance for college students' urban residents in 2008, and all medical expenses incurred during the period were borne by me.
College (seal, signature) student (signature):
date month year
Note: This commitment letter must be signed by the students themselves and kept by the college for the record.
Medical insurance 13 in order to ensure the safety and effectiveness of man and machine, our unit hereby guarantees that:
First, make sure to firmly establish the concept that the enterprise is the first person responsible for the quality of medical devices, strictly abide by the "Regulations on the Supervision and Administration of Medical Devices" and other relevant regulations, and standardize and produce in good faith according to law.
Second, ensure that production and sales are organized in strict accordance with standards.
Three, to ensure that medical devices must pass the inspection before leaving the factory, without inspection or unqualified products will never leave the factory.
Four, to ensure that the instructions, labels and packaging labels of medical devices comply with the relevant provisions of the state.
Five, to ensure that in strict accordance with the approved scope of application of products, to carry out medical device advertising and promotion activities, do not make false advertisements, do not mislead consumers.
Six, to ensure that the products after listing are tracked, once there is a quality problem or adverse event, immediately report it in time according to the regulations and take recall measures.
Seven, to ensure that the initiative to accept the supervision of food and drug supervision departments, all sectors of society and consumers, and actively cooperate with the supervision and inspection of relevant departments. If you violate the above commitments, deliberately evade supervision and cheat, all the consequences and responsibilities arising therefrom will be borne by our unit.
Commitment unit: XXX seal XXX
Legal Representative of Commitment Unit: XXX Signature XXX
Year, month, year, two thousand xx