In daily study, work or life, many people have had the experience of writing letters, and they are all familiar with letters. Letters have clear and specific purposes and recipients, and have fixed or Idiomatic format. So how do you write a good letter? The following are 10 pharmacy commitment letters that I have collected for everyone. They are for reference only. I hope they can help you. Pharmacy Commitment Letter Part 1
Dear leaders and colleagues in operating enterprises:
Drug safety is the most realistic, most concerned, and most direct interest issue for the people. It is the social responsibility and obligation of each of our pharmaceutical operating companies to improve the construction of corporate spiritual civilization, advocate civilized, law-abiding, and honest corporate management awareness and concepts, effectively safeguard the safety and effectiveness of medicines used by the people, and strive to create "100 trustworthy pharmacies" in Xiaoshan District. The quality and safety of food and drugs is related to social stability, economic development and people's physical and mental health.
In recent years, with the care and help of the government and drug regulatory authorities, our company has made great improvements in operation and management, and the quality of our employees has been improved. Now it is to establish a good image of pharmaceutical business enterprises as honest and trustworthy, fair transactions, serving the people and contributing to society. Taking "100 trustworthy pharmacies" as the execution criterion to ensure that the medicines we provide make the people safe and secure, we, Hangzhou Xiaoshan Tongchuntang Pharmaceutical Retail Co., Ltd. and our 43 pharmaceutical chain stores would like to express our sincere gratitude to all leaders, colleagues and The people of the whole district make the following solemn commitments:
1. Study seriously and fully implement the "Drug Administration Law", "Drug Administration Law Implementation Regulations" and "Pharmaceutical Quality Management Practices" and other relevant laws and regulations, abide by Observe the law and be strict with yourself. Purchase medicines from legal channels, make sure the bill and bill are consistent, and never deal in fake or substandard medicines.
2. Firmly establish the quality awareness of drug quality first and be responsible for people's health, engage in drug business activities in strict accordance with the requirements of the "Drug Quality Management Practices", and provide the general public with reliable and qualified drugs.
3. Consciously maintain the order of drug market operations, establish the marketing concept of fair competition, honesty and trustworthiness, and introduce drug characteristics and safe medication knowledge to consumers scientifically and realistically
Resolutely oppose unfair competition.
4. Pharmaceutical practitioners must consciously abide by professional ethics, be dedicated to their work, strive for first-class services, create a good drug purchasing environment, serve consumers with sincerity and love, establish a corporate image, and create a "safe drugstore" ".
5. Carry out drug promotion in strict compliance with the provisions of the country’s Advertising Law and Drug Administration Law, and do not make false advertisements or mislead or deceive consumers in any form. Strictly implement the national drug pricing policy, clearly mark prices, and do not deceive anyone.
Sixth, we must be brave enough to report illegal activities in pharmaceutical business activities, promptly report discovered adverse reactions to drugs and medical devices, maintain good drug circulation order, and ensure the safety and peace of mind of the people when taking drugs.
We must take it as our responsibility to create drugs that are honest and safe, so that the people can rest assured, and actively participate in the "Safety Pharmacy" activities, establish enterprises with integrity, promote development with integrity, and create more value. Give more back to society. Let us join hands, starting from me, starting from now. At the same time, we also hope to work with other pharmaceutical operating companies in the region to strengthen the promotion of corporate civilization and integrity, and make new contributions to building a harmonious and honest Xiaoshan! .
Hangzhou Xiaoshan Tongchuntang Pharmaceutical Retail Co., Ltd.
20xx.04.26 Pharmacy Commitment Letter 2
×× Municipal Food and Drug Administration:
p>
I am now aware of the relevant requirements of the State Food and Drug Administration’s “Notice on the Electronic Supervision of All Types of Essential Drugs” (State Food and Drug Administration [20xx] No. 194):
1. All winning bidders that produce essential drug varieties should join the electronic drug supervision network before March 31, 20xx. Before the essential drug varieties leave the factory, the manufacturer must print (stick) uniformly labeled drugs on the marketed products in accordance with regulations. Electronic supervision code, and data collection and submission through the supervision network.
2. Starting from April 1, 20xx, any species listed in the essential medicine catalog that has not been included in the network and has not been uniformly identified by the drug supervision code will not be allowed to participate in the bidding and procurement of essential medicines.
I solemnly promise not to produce essential drugs (or participate in the centralized bidding and procurement of essential drugs) for the time being. Before production (or before participating in centralized bidding and procurement), all work related to prescription process verification and electronic supervision of essential drugs will be completed to ensure the production quality of essential drugs and data collection and submission will be carried out through the electronic drug supervision network. Voluntarily accept supervision and inspection by drug regulatory authorities at all levels.
Promisor (signature of corporate legal representative):
(Official seal)
Year, month, day
This letter of commitment is made in triplicate. One copy should be sent to the provincial bureau, and one copy should be sent to the municipal (prefecture) bureau and the committed enterprise. Pharmacy Commitment Letter Part 3
1. Company Profile
Our company was established in March 20xx as an individual pharmaceutical retail company. Based on GSP, our company compiles and improves its quality management system.
At present, the company has 4 employees, including 2 pharmacists and 1 pharmacist. Pharmacy professional and technical personnel account for 100% of the total number. The allocation of pharmaceutical technicians can meet the requirements of drug operation quality management.
2. GSP organization and personnel structure
The enterprise sets up the company responsible person, purchasing, maintenance personnel, and warehouse managers as XX; the quality manager is XXX; the quality manager and the acceptance officer are XXX; the reviewers are XXXX and XXX; the salespersons are XXX and XXX. Clearly define the quality responsibilities of full-time quality personnel.
3. Personnel and training
In order to continuously improve the professional and technical quality of all employees, we have formulated a learning and training plan, and regularly organize all employees to learn drug management laws and regulations and professional and technical knowledge. Conduct assessments every six months and establish training files.
IV. Facilities and Equipment
Our company is equipped with computers and drug purchase, sales and inventory management software that meet relevant management requirements in accordance with the requirements of the new version of GSP, and is equipped with temperature and humidity detection equipment in the business premises. Equipment, now equipped with thermohygrometer and air conditioner. It is also equipped with rodent-proof, insect-proof, and fire-proof equipment. The business premises is clean and bright, with complete business shelves and counters.
5. Drug purchase and acceptance management
In accordance with the requirements of relevant laws and regulations such as the "Drug Administration Law" and "Pharmaceutical Goods Management Practices", the quality and legal qualifications of purchased drugs are checked. Review, and request copies of the drug GSP certification, drug business license (wholesale) and business license stamped with the company's official seal. The power of attorney should clearly specify the scope and period of authorization; a copy of the ID card of the drug salesperson; purchase For imported drugs, obtain copies of the "Imported Drug Registration Certificate" and "Imported Drug Inspection Report" from the supplier, and stamp them with the original seal of the supplier's quality management agency; imported drugs should have Chinese-labeled instructions. Implement an audit system for first-run enterprises and first-run drugs. The enterprise has established a drug purchase ledger, which records the drug purchase truly and completely to ensure that the tickets, accounts, and items are consistent, and then enters the records into the computer according to relevant procedures to complete all basic work.
Acceptance management: Acceptance personnel inspect and record the purchased drugs batch by batch in strict accordance with the relevant regulations based on the original vouchers and tax stamps. It mainly checks whether the accepted drugs meet the corresponding appearance quality standards. (1) Whether the outer packaging is firm and dry; whether the seals and seals are damaged; whether the outer packaging is marked with the common name, specifications, manufacturer, approval number, registered trademark, batch number, and validity period. Whether specific storage and transportation markings comply with pharmaceutical packaging requirements. (2) Whether each piece of inner packaging has a product certificate, whether the container is reasonable, whether it is damaged, whether the sealing is tight and qualified, the packaging writing should be clear, and the product name, specification, batch number, etc. must not be missing; the bottle label must be firmly affixed. (3) The generic name, ingredients, specifications, manufacturer name, approval number, production batch number, production date, validity period, etc. of the drug are clearly printed on the drug label and instructions. The label or instructions should also include indications or main functions, usage and dosage, contraindications, adverse reactions, precautions, and storage conditions. (4) The labels on the packages of the imported drugs that are accepted shall indicate the name, main ingredients and registration number in Chinese, with instructions in Chinese, and be accompanied by the "Imported Drug Registration Certificate", "Imported Medicinal Material Approval Document" and "Imported Drug Inspection Report". And stamped with a copy of the red seal of the supplier's quality management organization. Collect adverse drug reactions in a timely manner and report to the drug regulatory department immediately if any adverse reactions occur.
6. Drug storage, maintenance and display (retail) management.
When our company was first established, we strictly followed GSP requirements, created a storage and display environment to high standards, and decorated the business area in accordance with the latest municipal bureau standards, making the business premises spacious and bright. Shopping is convenient, the signs are eye-catching, and drugs are classified according to business conditions and GSP requirements. According to the performance and nature of the drugs, the warehouse is divided into areas to be inspected (yellow), combined drugs (green), unqualified drugs (red) and returns (yellow). Drugs and non-drugs, external drugs and internal medicines are stored in separate areas to facilitate operation and prevent errors and contamination incidents. Shelves, greenhouse thermometers, light-shielding facilities (curtains), and rodent-proof facilities (door seam seals) have been added to meet the requirements of the "seven preventions" (dust-proof, insect-proof, bird-proof, rodent-proof, moisture-proof, mildew-proof, and pollution-proof) . Lighting equipment that meets lighting requirements is installed. All business areas are equipped with air conditioners to ensure appropriate air humidity and temperature. At work, management is carried out in accordance with the store's "drug storage, maintenance and display management system", such as the "four separation principles" of displaying drugs and non-drugs separately, non-prescription drugs and prescription drugs, internal medicines and external medicines, etc. Special counters for special preparations containing ephedra are displayed and marked with warning slogans. The counters in the dismantling area are equipped with relevant dismantling tools. In addition, the temperature and humidity of the business area and warehouse are measured every morning and afternoon, and timely measures are taken to control if the requirements are not met; maintenance and inspection of the inventory and display of medicines are carried out regularly every month, and records are recorded as required. These measures can ensure the storage quality of medicines
7. Sales and after-sales service
In order to provide consumers with reliable medicines and high-quality services, companies must provide sales staff who are engaged in pharmaceutical retail work. Conduct business training and assessment. When selling medicines, according to the customer's requirements for the medicines purchased, the medicines will be handed over to the customers after verification, and a sales voucher will be issued. At the same time, the instructions for taking the medicines and contraindications will be explained to the customers in detail; the service agreement will be clearly stated in the business premises, the supervision telephone number will be announced, and the customer will be set up. Opinion Book. Customer evaluations and complaints will be resolved in a timely manner, and drug quality issues reported by customers will be taken seriously, recorded in detail, and handled in a timely manner.
8. Computer software system
The computer system is a well-known large company in China. Relevant modules comply with the application requirements of the new version of GSP, with automatic reminders for inventory levels every day, reminders for sales of products with near-expiration dates every month, automatic restrictions on relevant procurement, acceptance, sales and other activities for expired companies and expired drugs, and can be used for hemp-containing preparations. Automatically carry out limited sales and register name and ID card sales, etc. < /p>
The first is to scientifically summarize and organize relevant files and records; the second is to fill in the sales labels on the shelves in a standardized manner; the third is to re-clean the store; the fourth is to further inspect and standardize the classified management. . Through self-examination and self-correction activities, GSP management level has been further improved.
Through the GSP self-inspection, we believe that we have initially met the standard requirements. We are now submitting an application for certification. We welcome all leaders to come for inspection and guidance. Pharmacy Commitment Part 4
In order to effectively strengthen the quality management of pharmaceutical retail (chain) enterprises, promote law-abiding, standardized, honest and civilized operations, and promote the creation of civilized cities across the country, the following commitments are made:
< p> 1. Strictly abide by the "Code for Pharmaceutical Business Enterprises to Create a National Civilized City" formulated by the Municipal Food and Drug Administration, implement thirteen requirements in four aspects: beautiful environment, good management, quality and safety, and high-quality service, and abide by the "Twelve Don'ts" "Commits to carry out in-depth activities to create "No Counterfeit Drugs in Ten Thousand Stores in the Province", solidly promote the creation of civilized cities across the country, and ensure that no points are lost during inspections by the national evaluation team.2. Strictly comply with the requirements of the State Food and Drug Administration’s drug classification management regulations and sell prescription drugs based on prescriptions. When selling prescription drugs, they must be verified and signed by a licensed pharmacist or other qualified pharmaceutical technician before they can be sold.
3. Strictly implement relevant national regulations on the management of special drug compound preparations (including ephedrine-containing compound preparations, codeine-containing compound oral solutions, compound diphenoxylate tablets and compound licorice tablets), No more than 2 minimum packages may be sold at one time.
When you discover any abnormalities in purchases, you should report it to the Municipal Food and Drug Administration immediately to prevent fraud.
4. Strictly implement the responsibility of the "first person responsible for the enterprise", increase the implementation of the "Pharmaceutical Goods Management Practice", strengthen the training, education and management of enterprise employees, and ensure that the person responsible for drug quality On the job, consciously create and maintain a good pharmaceutical business order.
Company name: Linzhi Hengkang Affordable Pharmacy
Pledger:
February 21, 2015
Hangzhou Xiaoshan District Food Food and Drug Administration:
I hereby entrust Pei Feifei to apply to your bureau for administrative licensing matters on behalf of me (unit).
Authorization: Submit all materials related to this administrative license and sign for receipt
Various documents and licenses in the administrative licensing process.
This power of attorney is valid from October 1, 20xx until the licensing documents and certificates
are signed and received.
Principal (unit):
Legal representative (person in charge): (Signature)
Date, month, and year pharmacy commitment letter 5
This unit promises that the relevant materials submitted for the provincial-level basic medical insurance designated retail pharmacy contract signing application are true, legal, and valid. If there are any untruths, we are willing to bear all responsibilities and consequences.
Applicant unit legal person Wang Wenbin (signature) December 2, 20xx
Applicant unit Minhou First Branch of Kangle Pharmacy, Taijiang District, Fuzhou City
(Signature) Pharmacy Commitment Letter 6 on December 2, 20xx
To the leadership of xxx pharmacy:
In the past three years of work, I have no illegal or illegal records. , did not violate regulations or breach of contract to terminate the contract due to personal matters, and did not win the bid by fraud. During my time there were no pharmacies that were in the penalty stage of being ordered to close down, have their property taken over or frozen, or be suspended from participating in bidding activities.
I hereby promise.
Commitment person (signature):
Date: Year and month Pharmacy commitment letter 7
Hangzhou Xiaoshan District Food and Drug Administration:
I hereby entrust Pei Feifei to apply to your bureau for administrative licensing matters on behalf of me (unit).
Authorization: Submit all materials related to this administrative license, sign and receive various documents and licenses in the process of administrative licensing.
This power of attorney is valid from October 1, 20xx until the licensing documents and licenses are signed and received.
Client (unit):
Legal representative (person in charge): (Signature)
Date, month, and year of pharmacy commitment letter 8
Hangzhou Xiaoshan District Food and Drug Administration:
I hereby entrust Pei Feifei to apply to your bureau for administrative licensing matters on behalf of me (unit).
Authorization: Submit all materials related to this administrative license, sign and receive various documents and licenses in the process of administrative licensing.
This power of attorney is valid from October 1, 20xx until the licensing documents and licenses are signed and received.
Principal (unit):
Legal representative (person in charge): (Signature)
Year, month and day
Note: If the client is an individual, the client shall sign the name and date, and stamp with his fingerprint; if the client is a company, the legal representative or person in charge shall sign the name, date, and stamp with the official seal. Attached is a copy of the trustee’s ID card. Pharmacy Commitment Chapter 9
In accordance with the requirements of the "Drug Administration Law", "Pharmaceutical Business Quality Management Standards" and other relevant laws, regulations and rules, we ensure that the drugs sold in our store are of qualified quality and safe to use. , we conducted a self-examination on the relevant aspects of our store’s drug operation. The self-inspection situation is as follows:
1. Basic situation of the enterprise
The person in charge of the enterprise: xxxx, graduated from the xxxx department, professional title: Professional pharmacist.
Business address: xxxxx, business scope: biochemical products, Chinese herbal medicines, Chinese herbal medicine pieces, biological products (excluding preventive biological products), Chinese patent medicines, chemical pharmaceutical preparations, and antibiotic preparations. Economic nature: chain stores. The corporate purpose of "survive by quality, develop by integrity" follows the ethics of mutual benefit, mutual development, integrity first, and operating in accordance with the law.
2. Staffing situation:
In accordance with the requirements of relevant laws, regulations and rules for operating drugs, our store has established a corporate legal person xxx as the main responsible person; the quality manager, quality manager Person in charge of the organization: the quality leadership group headed by xxx, acceptance and maintenance personnel: xxx; medical shopping guide: xxx. The store *** has xxx employees.
3. Management of the training and assessment system and regular physical examination system for personnel in each position
1. According to the training requirements for corporate employees according to drug-related laws and regulations, the person in charge of store quality management shall conduct annual Develop an annual training plan, conduct legal, regulatory and professional knowledge training for store employees as planned, and establish training files.
2. In order to ensure the quality and safety of the drugs sold in the store, sales personnel and quality managers who are in direct contact with drugs must undergo at least one health examination every year. Only employees who pass the physical examination can continue to engage in their work. Physical examination Unqualified employees must stop working immediately and be transferred from their posts. and create their health records. 4. Overview of quality management system documents
In order to implement the management of the new version of GSP certification, we have formulated the following quality management system documents:
1. Store drug purchase and acceptance quality management system
p>
2. Store drug display management system
3. Store drug sales and prescription dispensing management system
4. Store drug disassembly and drug management system
5. Store drug maintenance inspection and management system
6. Hygiene and personnel health management system
7. Store service quality management specifications
8. Adverse drug reactions Reporting system
9. Unqualified drug management system
10. Quality management inspection and assessment system
11. Store management system of traditional Chinese medicine pieces
< p> 12. Refrigerated drug management system13. Computer management system
5. Facilities and equipment:
1. In accordance with the relevant regulations and requirements for operating drugs , the store operating area is 110 square meters, the store strictly implements zoning management, and the signs are obvious.
2. The store is clean, dry, and well-ventilated, with no pollution sources around. The store is equipped with facilities and equipment suitable for drug storage: air conditioners, shelves, containers, traditional Chinese medicine cabinets, dismantling medicine cabinets, dismantling tools, and clinical equipment. Preparation tools, computers, software, mouse traps, fire extinguishers, freezers, direct-reading thermometers and hygrometers, scales, and light-proof curtains.
6. Computer System Overview
With the implementation of GSP certification, in order to better manage and sell, we have upgraded the computer software and compiled a new version according to the new version of GSP certification software. Record ledgers and recording forms were compiled according to GSP requirements, and quality management system documents were re-established, a sound quality management system and working procedures were established, and all work was incorporated into modern computer management, effectively ensuring the standardized operation of store work. .
7. Management and operational procedures for drug procurement, acceptance, storage, maintenance, and sales
1. Purchase of drugs
Purchase of drugs Strictly follow the quality management system of this pharmacy, strengthen the review of the quality assurance system of supplier companies, require suppliers to provide copies of the "Pharmaceutical Business License" and "Business License" with official seals, and establish files for supplier companies , strengthen the qualification review of the supplier's drug sales personnel, and sign a quality assurance agreement with the supplier; when purchasing imported drugs, the supplier is required to provide an "Imported Drug Registration Certificate" stamped with the original seal of the supplier's quality management agency or Copies of "Pharmaceutical Product Registration Certificate" and "Imported Drug Inspection Report": Check quality from the source.
2. Acceptance of drugs
In accordance with the corresponding laws and regulations, the quality terms and quality standards of the contract, we strictly inspect the appearance, shape, packaging and labeling of the drugs. The request will be firmly rejected.
3. Standardize drug display management
According to GSP requirements, pharmacies standardize drug display management, so that they can be classified according to their uses, and at the same time, they should do a good job in distinguishing drugs and non-drugs, internal medicines and External medicines and medicines that are prone to odor are stored separately, prescription medicines and non-prescription medicines are stored in separate cabinets, and disassembled medicines are stored in special counters, and the signs are obvious and clear. Inspect the displayed drugs every month and record them truthfully.
4. Pay attention to the maintenance of drugs
According to the quality management system of the pharmacy, I store and display drugs reasonably according to the storage conditions of the drugs, and record the business on time every morning and afternoon. The temperature and humidity of the place should be taken into account in a timely manner when the temperature and humidity do not meet the drug storage requirements. At the same time, regular inspections of general drugs in stock are carried out quarterly, and key maintenance varieties are inspected monthly. Maintenance files are also established for key maintenance varieties, and maintenance records must be true, complete, and standardized.
5. Do a good job in the sales of drugs
In order to standardize the behavior of the drug business and provide consumers with reliable drugs and quality services, the preparation of prescription drugs shall be reviewed and reviewed by the prescription. Other drugs Sales staff can insist on asking questions and do the "three questions", that is, asking about the condition, asking about gender, and asking about age, that is, explaining the dosage, dosage, and precautions. According to the name of the medicine purchased by the customer, , after the specifications, quantity, and price are verified, the medicines are handed over to customers to ensure that people use medicines safely and effectively. We also provide consulting services to guide customers on the safe and rational use of medications.
6. Management of returned drugs
1. Returned drugs are kept by dedicated personnel, stored in special areas, and recorded in special accounts.
2. All returned and exchanged drugs should be re-accepted, a clear conclusion should be made, and they can only be sold if they are qualified.
3. Any substandard drugs or problematic drugs should be contacted in time with the supplier and handled properly.
4. Problematic returned drugs should be stored in the return area or pending area.
5. The return records are complete, accurate, standardized, complete with procedures and signatures, and are kept in accordance with regulations.
7. Complaint handling
Pharmacies should clearly state the service agreement in the business store, publish the supervision telephone number and set up a customer opinion book; take customer opinions seriously and take effective improvement measures in a timely manner. Records of quality inquiries, complaints, drug returns and services provided are true, complete and properly kept.
8. Adverse drug reaction reporting system
1. Clear concepts, clear responsibilities, and standardized procedures.
2. Effectively collect adverse reaction information of drugs.
3. Report adverse drug reactions in a timely manner.
4. The records are complete, accurate and standardized.
8. Bill management system
1. Strengthen bill management and prevent the loss of documents. Whoever collects the bills is responsible. The economic losses caused by the loss of bills will be compensated by the responsible person.
2. Compliance bill materials are used for settlement, and the finance department has the right to refuse reimbursement for informal bills. () In response to the notice from your department, the Municipal Sanli Pharmaceutical Company held a timely meeting to communicate and arrange the work, and required our subordinate operating companies to promptly carry out self-examination and self-correction within the department, in accordance with the provisions of the National Food and Drug Supervision and Administration Law and GSP management. , conduct strict self-examination and write self-inspection reports based on their respective situations. Our fifth department of Sanli Pharmaceutical carefully conducted a self-examination in accordance with the requirements. We now report the results of the self-examination as follows:
After we received the notice, all employees took action, under the leadership of the person in charge of our department , conducted a comprehensive inspection of the interior of the store, which took one day. Finally, we summarized the inspection results and found the following problems:
1. The signs in the store that remind and warn customers are aging and losing their beauty. We made the changes promptly and now have new warning signs in place.
2. The overall hygiene of the pharmacy is okay, but some blind spots are not cleaned well enough. For example, the bottom compartment of each counter was not cleaned thoroughly. The salesperson was criticized and educated on the spot and asked to make corrections in the future.
3. There was no timely attention to the medicines near the expiration date, and the problem was only discovered when customers saw it. Be sure to carefully conduct display inspections in the future.
4. The writing of temperature and humidity records is not standardized enough, and some fonts are illegible.
In short, through this inspection, we discovered various problems in our work. We must take this inspection as an opportunity to make serious rectifications, work hard, and do a better job in operating our store to satisfy customers and allow the masses to truly use the medicine.
3. The receipt and cancellation of bills must be completed in accordance with the regulations for handover, registration and signature.
4. Invoices should be controlled effectively, classified and archived, and properly kept.
9. Main problems and corrective measures
In order to better implement GSP, our store conducted a comprehensive self-examination through reporting, site visits, information checking, investigation and inquiry. Through self-examination, we believe that we have basically complied with the requirements of the "Pharmaceutical Goods Management Practice" and its "Implementation Rules", but there are still certain gaps in some aspects: (for example: first, pharmacy staff lack consciousness of business; Second, the service quality is not standardized enough).
Regarding the above existing problems, our store has done careful analysis and research, formulated measures, and required personnel in each position to strengthen their business learning consciousness and strive to become familiar with various business knowledge in a short period of time. We will strive to improve service quality. At the same time, we will use this GSP certification as an opportunity to further enhance quality management awareness, increase quality management efforts, continuously strengthen and improve the hardware construction and software management of the entire store, and strive to gradually improve the quality management work of our store. Towards modernization, standardization and institutionalization, we will make due contributions to ensuring the safety and effectiveness of medication for the broad masses of the people. Pharmacy Commitment Letter Part 10
1. Implement quality responsibility. Conscientiously implement the "Drug Administration Law", "Drug Administration Law Implementation Regulations" and a series of national relevant drug laws and regulations, effectively fulfill the obligations of the first person responsible for drug safety, and further establish and improve the drug quality and safety assurance system to ensure public health. Responsible attitude, strengthen daily quality management, and ensure drug safety.
2. Strict behavioral self-discipline. Unqualified medicinal capsules and other medicinal excipients will never be sold; the medicines and medicinal hollow capsules sold must pass the inspection by the drug inspection agency before they can be sold.
3. Strengthen safety management. We will further establish and improve the drug safety guarantee mechanism, fully implement drug operation quality management standards, strive to improve the level of standardized operation, increase the intensity of adverse drug reaction detection and reporting, eliminate drug safety hazards, and put an end to drug safety accidents.
4. Adhere to integrity and law-abiding. Take integrity as the foundation, firmly establish a sense of integrity, abide by contracts and keep promises, do not make false propaganda, and make pharmaceutical and device advertising reasonable, legal and compliant. Strengthen the concept of legality, consciously operate in accordance with the law, and win the trust of society.
5. Consciously accept supervision. Actively cooperate with the daily drug safety supervision, special inspections, risk monitoring and emergency response implemented by the food and drug regulatory authorities in accordance with the law, and consciously accept supervision from the news media and all walks of life. Strive to improve service levels and make due contributions to the healthy development of Wuning’s pharmaceutical industry.
6. Carry out extensive publicity. Actively participate in the promotion and lectures of drug safety science knowledge
, strive to improve the quality and safety awareness of all employees, conscientiously implement the concept of "selling qualified products is glorious, selling fake and inferior products is shameful", and provide scientific consumption information , promote rational drug use and healthy living behaviors, and safeguard the legitimate rights and interests of drug operators and consumers.
Commitment company (seal):
Commitment person (signature):
Year, month, day