In the usual study, work or life, many people have had the experience of writing letters, letters are no stranger to it, letters have a clear and specific purpose and acceptance of the object, and have a fixed or customary format. Then how to write a good letter? The following is my collection of pharmacy commitment letter 10, just for reference, I hope it can help you.
Pharmacy letter of commitment Part 1Dear leaders and colleagues in the business enterprises:
Drug safety is the most realistic, most concerned about the people, the most direct interests of the issue. Improve the spiritual civilization construction of enterprises, advocate civilization, law-abiding, honest enterprise management consciousness and concept, effectively maintain the people's medication safety and effective, and create Xiaoshan District, "one hundred assured drugstores" is the social responsibility and obligation of each of our drug business enterprises. 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, in the government and drug supervision and management departments to care and help, our company in the operation and management has made great progress, the quality of practitioners has been improved. Now in order to establish the drug business enterprises honest and trustworthy, fair trade, service to the public, dedication to the community's good image. To "100 assured drugstores" for the implementation of the guidelines to ensure that the drugs we provide the people safe, secure, I Hangzhou Xiaoshan Tongchuntang Medicine Retail Limited Liability Company and our 43 drug chain stores to the leaders, colleagues and the whole region to make the following solemn commitment:
First, seriously study, fully implement the "Drug Administration Law", "Drug Control Law", "Drug Control Law", "Drug Control Law", "Drug Control Law", "Drug Control Law", "Drug Control Law", "Drug Control Law", and so on. Fully implement the "Drug Administration Law", "Drug Administration Law Enforcement Regulations" and "Drug Quality Management Code" and other relevant laws and regulations, abide by the law, and be strict with themselves. Purchase drugs from legitimate channels, to achieve the ticket account goods in line, and never operate fake or shoddy drugs.
Second, firmly establish the quality of drugs first, the quality of people's health is responsible for the awareness, in strict accordance with the "Code of Practice for the Management of Pharmaceutical Quality," the requirements of the drug business activities, for the general public to provide assured that qualified drugs.
Third, consciously maintain the order of the drug market, establish fair competition, honest and trustworthy marketing concepts, scientific and factual information to consumers about the characteristics of drugs and safe use of medication
knowledge, and resolutely oppose unfair competition.
Fourth, drug practitioners should consciously abide by professional ethics, dedication, and strive to create first-class service, create a good environment for purchasing medicines, with sincerity, love for consumer services, tree corporate image, create a "safe pharmacy".
Fifth, strictly in accordance with the provisions of the State "Advertising Law" and "Drug Administration Law" to carry out drug publicity, do not make false advertisements, not in any form of misleading and deceiving consumers. Strictly implement the national drug pricing policy, clearly marked prices, and the child and the old man.
Sixth, the illegal behavior of drug business activities should be brave to report, the discovery of drugs, medical equipment adverse reactions should be reported in a timely manner, to maintain a good order of drug circulation, to ensure that the people's medication safety and peace of mind.
We have to create a drug integrity, safety, so that the people can rest assured that their own responsibility, and actively participate in the "assured that the drugstore" activities, in good faith to establish the enterprise, in good faith to promote the development of more value creation, more return to society. Let's join hands, start from me, start from now, and also hope that with the other drug business enterprises in the region, hand in hand to strengthen the enterprise civilization and honesty advocacy efforts to build a harmonious and honest Xiaoshan to make new contributions!
Hangzhou Xiaoshan Tongchuntang Medicine Retail Limited Liability Company
20xx.04.26
Pharmacy Commitment Part 2× × City Food and Drug Administration:
I am now aware of the State Food and Drug Administration's "notice on the work of all varieties of electronic monitoring of essential medicines" (SFDA [20xx] 194) the relevant requirements:
I am now aware of the State Food and Drug Administration "on essential medicines for all varieties of electronic monitoring work" (SFDA [20xx] 194)
Second, April 1, 20xx onwards, included in the directory of essential medicines, varieties, not into the network and did not use the unified logo of the drug regulatory code, are not allowed to participate in the bidding and procurement of essential medicines.
I solemnly promise not to produce essential drugs (or not to participate in the centralized bidding and procurement of essential drugs). Before the production (or to participate in the centralized bidding and procurement before) will complete the prescription process verification and electronic monitoring of essential medicines and other related all work to ensure that the quality of production of essential medicines and through the electronic monitoring of drugs network for data collection and reporting work. Voluntarily accept the supervision and inspection of drug supervision and management departments at all levels.
Commitment (signed by the legal representative of the enterprise):
(official seal)
Year Month
This commitment in triplicate. A copy of the provincial bureau, the city (prefecture) bureau and the commitment of the enterprise to take a copy.
Pharmacy commitment letter Part 3
First, the enterprise profile
The enterprise was established in March 20xx, is an individual drug retail enterprise. This enterprise takes GSP as a guideline to prepare and improve the enterprise quality management system.
At present, the enterprise has 4 employees, including 2 pharmacists, 1 pharmacist, pharmacy professional and technical personnel accounted for 100% of the total number of people. Pharmacy technicians can adapt to the requirements of quality management of drug business.
Second, the GSP organization and personnel structure
The enterprise set up the person in charge of the enterprise, purchasing, maintenance staff, warehouse managers for XX; the person in charge of the quality of XXX; quality control administrator, acceptance of XXX; reviewer XXXX, XXX; salesman XXX, XXX clearly defined the quality of quality personnel quality responsibility.
Third, personnel and training
In order to continuously improve the professional and technical qualities of all employees, the development of learning and training programs, regular organization of all employees to learn drug management laws and regulations and professional and technical knowledge, every six months for an assessment, and the establishment of training files.
Four, facilities and equipment
The enterprise in accordance with the new GSP requirements are equipped with computers and meet the relevant management requirements of the drug inventory management software, in the business premises configured to detect the temperature and humidity of the equipment, is now equipped with temperature and humidity meter, air conditioning. And equipped with rodent-proof, insect-proof, fire prevention equipment. The business place is clean, bright, business shelves, counters are available.
Five, drug purchase, acceptance management Management
In accordance with the "Drug Administration Law" and "Drug Administration Quality Management Standard" and other relevant laws and regulations, the purchase of drugs for quality and legal qualifications of the audit, and to obtain the official seal of the drug GSP certification, drug license (wholesale) and business license. Business license (wholesale) and a copy of the business license, the power of attorney should specify the scope of authorization and authorization period; copies of drug sales personnel's identity cards; the purchase of imported drugs, the supply unit to obtain the "imported drug registration certificate", "imported drug inspection report" copy, and stamped with the original seal of the supplier's quality management agencies; imported drugs should be marked with a Chinese language instruction manual. The first enterprise and the first drug to implement the audit system. Enterprises have established a drug purchase account, the account true and complete record of drug purchases, to achieve the ticket, account, things match, and then according to the relevant procedures to enter the computer to do the basic work.
Acceptance management: acceptance personnel on the purchase of drugs, according to the original documents and tax stamps, in strict accordance with the relevant provisions of the batch-by-batch inspection and acceptance and record. Mainly check whether the acceptance of the drugs in accordance with the corresponding appearance of quality standards. (1) Whether the outer package is firm and dry; whether the sealing label and seal are broken or not; whether the outer package indicates the generic name, specification, manufacturer, approval number, registered trademark, batch number and expiration date. For specific storage and transportation mark whether in line with the requirements of pharmaceutical packaging. (2) Whether there is a certificate of product conformity in each piece of inner packaging, whether the container is reasonable, whether there is any breakage, whether the sealing is qualified, the package should be clear handwriting, name, specification, batch number, etc. shall not be missing items; bottle labeling should be firmly affixed. (3) Drug labeling instructions clearly printed with the generic name of the drug, ingredients, specifications, the name of the manufacturer, approval number, production lot number, production date, expiration date, etc.. Labeling or instructions should also be indications or functions, dosage, contraindications, adverse reactions, precautions and storage conditions. (4) acceptance of imported drugs and their packaging labels in Chinese indicating the name, the main ingredients and registration number, with Chinese instructions, with "imported drug registration certificate", "imported medicinal materials batch" and "imported drug inspection report", and stamped with a copy of the supplier's quality management organization red seal. Timely collection of adverse drug reactions, the emergence of adverse reactions immediately reported to the drug regulatory authorities.
Six, drug storage, maintenance and display (retail) management.
I enterprise in the beginning of the construction of the strict requirements of the GSP, a high standard of storage and display environment, according to the city council of the latest standard decoration of the business area, to achieve a spacious and bright business premises. Convenient shopping, eye-catching signs, according to the business situation and the requirements of GSP, the drugs are categorized. And according to the drug performance and nature of the partition, classification, the implementation of the color-coded management, the warehouse is divided into pending inspection area (yellow), the drug area (green), unqualified drugs area (red) and return area (yellow), so that the drugs and non-drugs, drugs for external use and internal use of drugs stored in separate areas, so as to facilitate the operation, to prevent errors, contamination of the incident occurred. Shelves, greenhouse meters, light protection facilities (curtains), anti-rodent facilities (door seals) have been added to meet the requirements of the "seven defenses" (dust, insects, birds, rodents, moisture, mold, pollution). Lighting equipment that meets the lighting requirements has been installed. The business areas are equipped with air conditioners to ensure proper air humidity and temperature. In the work in accordance with the store's "drug storage, maintenance and display management system" for management, such as drugs and non-drugs are displayed separately, over-the-counter drugs are displayed separately from prescription drugs, drugs for internal use are displayed separately from drugs for external use, such as the "four separate principles" of categorization and display, including Special preparations containing ephedra preparations are displayed in special cabinets with warning slogans, and special cabinets in the zero-removal area are equipped with relevant zero-removal tools. In addition, the temperature and humidity of the business area and the warehouse are measured every day in the morning and afternoon, and timely measures are taken to regulate the temperature and humidity when it is not in accordance with the requirements; the maintenance and inspection of the stock and the display of drugs are carried out on a regular basis every month and recorded according to the requirements, etc. These measures can ensure the storage quality of the drugs. These measures can ensure the quality of the storage of drugs
seven, sales and after-sales service
In order to provide consumers with assured that the drugs and quality of service, the enterprise engaged in the retail sale of medicines sales staff, business training and assessment. The sales of drugs, for customers to request the purchase of drugs, after checking the drugs with the customer, and issue sales vouchers, while detailed to the customer to explain how to take the drugs and contraindications, etc.; in the business place to express the service convention, publish the supervision telephone and set up the customer opinion book. The customer's evaluation and complaints are resolved in a timely manner, and the quality of drugs reflected by the customer is taken seriously, recorded in detail and handled in a timely manner.
Eight, computer software systems
Computer systems for the domestic well-known large companies. Relevant modules in line with the new version of the GSP application requirements, every day on the stock of automatic reminders, monthly inventory of near-expiry products can be done to remind the sale of reminders, the expiration of the enterprise and the expiration of the drug automatically limit the relevant procurement acceptance of sales and other activities, the preparation of preparations containing cannabis can be automatically limited to the registration of the name and ID card sales, and so on.
Nine, self-examination
I set up a self-examination team in the pharmacy, led by XXX, the quality of the person in charge of the implementation of the GSP management of self-examination and rectification of the situation:
First, the relevant archives, records, scientifically summarized and collated; the second is to fill out the sales label specification on the shelves; the third is to the storefront Health re-cleaning; Fourth, the classification of the management of the situation for further inspection and standardization. Through the self-examination and self-correction activities GSP management level has been further improved.
Through the GSP self-check, we believe that we have initially met the standard requirements, and is now applying for certification, welcome to the leaders to come to inspect and guide.
Pharmacy Commitment Part 4
In order to effectively strengthen the quality management of pharmaceutical retail (chain) enterprises, to promote law-abiding, standardized, honest and civilized operation, and to promote the creation of a national civilized city, we have made the following commitments:
First, strictly abide by the City Food and Drug Administration formulated the "Drug Business Enterprises to create a national civilized city norms," the implementation of the environment is beautiful, excellent management, quality and safety, Service quality four aspects of the thirteen requirements, abide by the "twelve no" commitment to carry out in-depth "the province's 10,000 stores without fake drugs" to create activities, and solidly promote the creation of a national civilized city, to ensure that the national assessment team inspection does not lose points.
Second, in strict accordance with the requirements of the State Food and Drug Administration drug classification and management regulations, with prescription sales of prescription drugs. Sales of prescription drugs, must be certified by a licensed pharmacist or other accredited pharmacy technicians to verify the correctness and sign to confirm before sales.
Third, the strict implementation of the relevant provisions of the State on the management of special drugs compound preparations (including ephedrine-containing compound preparations, codeine-containing compound oral solution, compounded difenocoumarol tablets and compounded licorice tablets), the sale of a time shall not be more than the minimum of two packages. When the purchase of abnormalities and other circumstances are found, they should be immediately reported to the Municipal Food and Drug Administration to eliminate the occurrence of abuses.
Fourth, the strict implementation of the "enterprise the first responsible person" responsibility to increase the "Drug Business Quality Management Code" implementation efforts to strengthen the enterprise practitioners training, education and management, to ensure that the person in charge of the quality of drugs on duty, consciously create and maintain a good order of drug business.
Enterprise Name: Linzhi Hengkang Affordable Pharmacy
Committed by:
February 15, 2005
Hangzhou Xiaoshan District Food and Drug Administration:
I hereby entrust Pei Fei Fei to apply on behalf of me (the unit) to your office for administrative licensing matters related to the matter.
Entrusted authority: submit all materials related to this administrative license, sign for
administrative licensing process of all kinds of documents and licenses.
This power of attorney is valid from October 01, 20xx to the license documents and licenses
license signing and receipt of the end.
Client (unit):
Legal representative (person in charge): (Signature)
Month of the year
Pharmacy Commitment Part 5The unit is committed to the provincial level of the basic medical insurance fixed-point retail pharmacy signing the application of the relevant materials are true, legal and effective, if false, willing to bear all the responsibilities and consequences.
The legal person of the application unit Wang Wenbin (signature) December 2, 20xx
The application unit Fuzhou City, Taijiang District, Kangle Pharmacy Minhou first branch
(signature) December 2, 20xx
Pharmacy commitment letter Part 6To the leadership of the xxx Pharmacy:
I in the last three years of work, no violation of laws, violations of the adverse records , no violation or breach of contract termination due to the application of personal matters, no fraudulent winning bid. No pharmacy during my work is in the penalty phase of being ordered out of business, or property is taken over or frozen, or suspended from participating in bidding activities.
Hereby undertake.
Commitment (signature):
Date: January
Pharmacy Commitment 7Hangzhou Xiaoshan District Food and Drug Administration:
I hereby entrust Pei Fei Fei to apply to your office on behalf of me (unit) to deal with matters related to administrative licensing matters.
Entrusted authority: submit all materials related to this administrative license, sign and receive all kinds of documents and licenses in the process of administrative licensing.
This power of attorney is valid from October 01, 20xx to the permit documents and licenses signed and received.
Client (unit):
Legal representative (person in charge): (Signature)
Month of the year
Pharmacy Commitment 8Xiaoshan District, Hangzhou City, Food and Drug Administration:
I hereby entrust Pei Fei Fei to apply to your bureau on behalf of me (the unit) to handle the matters related to administrative licensing matters.
Entrusted authority: submit all the materials related to this administrative license, sign and receive all kinds of documents and licenses in the process of administrative licensing.
This power of attorney is valid from October 01, 20xx to the permit documents and licenses signed and received.
Client (unit):
Legal representative (person in charge): (signature)
Month of year
Note: If the client is an individual, the name and date signed by the client himself, and affixed with a hand seal; if the client is a business, the legal representative or person in charge of the name and date signed and affixed with an official seal. With a copy of the identity card of the delegate.
Pharmacy commitment 9
According to the "Drug Administration Law", "Drug Business Quality Star Management Code" and other relevant laws and regulations and rules, to ensure that my store operated by the drug 'quality qualified, the use of safe, my store drug operation of the relevant aspects of the self-examination, the self-examination of the situation is as follows:
A, the basic situation of the enterprise
The person in charge of the enterprise: xxxx, graduated from the Department of xxxx, title: professional pharmacist. Business address: xxxxx, business scope: biochemical products, Chinese herbal medicines, Chinese medicine tablets, biological products (excluding preventive biological products), proprietary Chinese medicines, chemical preparations, antibiotic preparations. Economic nature: chain stores. "Quality of survival, integrity and development" of the enterprise purpose, follow the mutual benefit, *** with the development, integrity first, according to the operation of the ethical norms.
Second, the staffing situation:
In accordance with the requirements of the relevant laws, regulations and rules for the operation of medicines, our store to establish the enterprise legal person xxx as the main responsible person; the person in charge of the quality, the quality of the organization responsible for the quality of: xxx mainly quality leadership group, acceptance, maintenance personnel: xxx; medicine shopping guide: xxx. Store **** has xxx employees.
Third, the positions of personnel training and assessment system and the management of regular medical examination system
1, according to the drug-related management laws and regulations on the training requirements for employees of the enterprise, the person in charge of quality management of the store each year to develop the annual training program, and according to the plan of the store staff training in laws, regulations and professional knowledge, and at the same time, the establishment of training The file.
2, in order to ensure the quality and safety of the drugs operated by the store, the annual direct contact with the drug sales staff and the quality of the person in charge of at least one health checkup, only qualified employees can continue to engage in their work, the physical examination of the employees failed to stop working immediately, transfer out of the post. And establish its health records. Fourth, the quality management system document overview
In order to implement the management of the new GSP certification, we develop the following quality management system documents:
1, store drug purchase and acceptance of quality management system
2, store drug display management system
3, store drug sales and prescription dispensing management system
4, stores Pharmaceuticals and drugs split drug management system
5, store drug maintenance and inspection management system
6, hygiene and personnel health management system
7, store service quality management standard
8, adverse drug reaction reporting system
9, substandard drug management system
10, quality management work inspection and assessment system
11, quality management work inspection and assessment system11, the store Chinese medicine tablets management system
12, refrigerated drug management system
13, computer management system
V. Facilities and equipment:
1, in accordance with the relevant provisions of the regulations and requirements of the operation of the drug, the store business area of 110 square meters, the store strictly implement the The management of the area, the sign is obvious.
2, the store is clean, dry, well-ventilated, no pollution sources around, the store is equipped with facilities and equipment suitable for the storage of medicines: air conditioning, shelves, cabinets, Chinese medicine cabinet, demolition of medicine cabinet, demolition of tools, clinical prescription concoctions tools, computers, software, rodent traps, fire extinguishers, cold cabinets, direct-reading thermo-hygrometer, weighing support, light curtains.
Six, computer system overview
With the implementation of the GSP certification, we in order to better management and sales, computer software upgrades, in accordance with the new version of the GSP certification software compiled a new record ledger, record forms, according to the provisions of the GSP requirements, to re-compile the quality management system documents, the establishment of a sound Quality management system, work procedures, and the work into the modernization of microcomputer management, effectively ensure the standard operation of the store work.
VII, drug purchasing, acceptance, storage, maintenance, sales and other aspects of the management and operational procedures
1, the purchase of drugs
The purchase of drugs is strictly in accordance with the implementation of the quality management system of the drugstore, to strengthen the quality of the supplier enterprise quality assurance system of the audit, require the supplier to provide a stamped, stamped, stamped, stamped, stamped, stamped, stamped, stamped, stamped, stamped, stamped, stamped and stamped. Audit, the supplier is required to provide stamped "drug license" and "business license" copy, the establishment of the supplier enterprise files, strengthen the qualification audit of the supplier's drug sales staff, and signed a quality assurance agreement with the supplier; purchase of imported drugs require the supplier to provide the supplier to cover the original seal of the quality management body of the supplier "Imported Drugs Certificate of Registration" or "Pharmaceutical Products Certificate of Registration", "Imported Drugs", "Inspection Report" copy. The company has also signed a quality assurance agreement.
2, the acceptance of drugs
We in accordance with the corresponding laws and regulations, the quality of the contract terms and quality standards, the appearance of the shape of the drugs, packaging and labeling strict acceptance, does not meet the requirements of the resolute to be rejected.
3, standardize drug display management
The pharmacy according to the GSP requirements, standardize the management of drug display, to do according to the use of classification of placement, and at the same time to do a good job of drugs and non-drugs, medicines and drugs for external use, easy to cascade of drugs are stored separately, prescription drugs and over-the-counter medicines in separate cabinets, as well as the demolition of drugs in special counters, and marked obvious, Clearly labeled. The monthly inspection of the display of drugs and truthful records.
4, pay attention to the maintenance of drugs
According to the quality management system of the pharmacy, I according to the conditions of the drug storage of drugs for a reasonable storage and display, daily morning and afternoon on time to record the temperature and humidity of the place of business, the temperature and humidity do not meet the requirements for the storage of medicines, and then promptly take measures to regulate. At the same time, the quarterly inventory of general drugs to carry out inspection, the key maintenance varieties of monthly inspection, the key maintenance varieties also set up maintenance files, maintenance records to achieve real, perfect, standardized.
5, do a good job in the sale of drugs
In order to standardize the behavior of the pharmaceutical industry, to provide consumers with assured that the drugs and quality service, prescription drugs dispensed by the prescription audit review, other drug sales staff can adhere to ask the disease, to do the "three questions", namely: ask the condition, ask the sex, ask the drug sales staff to do the "three questions", namely: ask the disease, ask the sex, ask the drug sales staff to do the "three questions". Ask the condition, ask the gender, ask the age of the "three account", that is, account for service, account for the dosage, account for precautions, according to the name of the drugs purchased by the customer, specifications, quantities, prices, after checking, the drugs will be handed over to the customer, to ensure that the people safe and effective medication. And provide consulting services to guide customers to safe and rational use of drugs.
6, the return of drug management
1, the return of drugs in the custody of a person, special area storage, special account records.
2, all returned medicines should be re-examined, a clear conclusion, qualified before re-sale.
3, all unqualified drugs or problematic drugs should be promptly contacted with the supplier, properly handled.
4. Problematic returned medicines should be stored in the return area or pending disposal area.
5, the return record is complete, accurate, standardized, complete procedures, signatures, and kept in accordance with regulations.
7, complaint handling
Pharmacies in the business store hall express service conventions, publish supervision telephone and set up the customer opinion book; serious treatment to deal with the customer's views, and take timely and effective improvement measures. Quality inquiries, complaints, drug returns and the provision of service programs and other records are true and complete, and properly stored.
8, adverse drug reaction reporting system
1, the concept is clear, clear responsibilities, standardized procedures.
2, effective collection of adverse drug reaction information.
3, the discovery of adverse drug reactions reported in a timely manner.
4, complete, accurate and standardized records.
Eight, bill management system
1, strengthen the management of bills, to eliminate the loss of documents, who receives who is responsible for the economic losses caused by the loss of bills by the responsible person to compensate.
2, compliance bill material for settlement, finance has the right to refuse to hold informal bills for reimbursement. () Receiving the notice of your office, the city Sanli Pharmaceutical Company timely meeting to convey the layout of the work, requiring our subordinate business enterprises to grasp within the department to carry out self-examination and self-correction work, in contrast to the provisions of the State Food and Drug Administration Law and the GSP management, strict self-examination, and according to their respective situations to write a self-examination report. We, Sanli Pharmaceuticals Department V, in accordance with the requirements, seriously carried out self-inspection, and now report the results of the self-inspection as follows:
After we received the notice, all the staff acted under the leadership of the person in charge of our department, and carried out a comprehensive inspection inside the store, and the inspection took one day, and finally we summarized the results of the inspection and found that there are the following problems:
1, the store prompts, warns the customers of the The sign is aging and losing its beauty. We made timely changes, and now have replaced the new warning signs.
2, the overall health of the drugstore can be, but some of the dead ends of the health cleaning is not clean enough. For example, the counter of the bottom of the grid, inside the health cleaning is not complete. The salesman was criticized and educated on the spot, and asked him to make sure to correct it in the future.
3, near-expiry drugs did not pay attention to timely, so that customers see the problem only found. In the future, we will be sure to check the display carefully.
4, temperature and humidity record writing is not standardized, some of the font scribbles can not see.
In short, through this inspection, we found that there are such and such problems in our work. We must take this inspection as an opportunity to seriously rectify and work hard to do a better job of my store's operation, so that customers are satisfied, so that the masses can really use the assured drug.
3, the receipt and cancellation of bills must be in accordance with the provisions of the handover registration and signing procedures.
4, effective control of bills, categorized files, properly stored.
Nine, the main problems and corrective measures
In order to better implement the GSP, I store through the report, look at the scene, check the information, investigate the inquiry and other ways to carry out a comprehensive self-examination. Through self-examination, we believe that has basically met the "Drug Administration Quality Management Standard" and its "Implementation Rules" requirements, but there are still some gaps in certain aspects: (eg: First, the pharmacy staff lack of self-consciousness about the business, the second is the quality of service is not standardized).
On the above problems, I store to do a serious analysis of the study, the development of measures to require all positions to strengthen the business learning conscientiousness, and strive to familiarize themselves with the mastery of the business knowledge in a relatively short period of time, and strive to improve the quality of service, and at the same time, we will be the GSP certification as an opportunity to further enhance the awareness of quality management, and increase the quality of the work of the management of the hardware and software construction of the whole store to strengthen and improve management. Management continue to strengthen and improve, and strive to make my store quality management work gradually towards modernization, standardization and institutionalization, in order to ensure that the general public with safe and effective medication to make its due contribution.
The pharmacy commitment 10
First, the implementation of quality responsibility. Conscientiously implement the "Drug Administration Law", "Drug Administration Law Enforcement Regulations" and a series of national laws and regulations on drugs, and effectively fulfill the obligations of the first person responsible for drug safety, and further establish and improve the quality and safety assurance system of medicines, to the public health responsible attitude, strengthen the daily quality management, to ensure the safety of medicines.
Second, strict behavior self-discipline. Never sell unqualified pharmaceutical capsules and other pharmaceutical excipients; sold drugs and pharmaceutical hollow capsules must be qualified by the drug testing organizations before selling.
Third, strengthen the safety management. Further establish and improve the drug safety guarantee mechanism, the full implementation of the drug quality management standard, and strive to improve the standardized level of operation, increase the adverse drug reaction detection report, eliminate drug safety hazards, to eliminate drug safety accidents.
Fourth, adhere to the integrity and law-abiding. Integrity as the fundamental, firmly establish the sense of integrity, contract, trustworthy, do not do false propaganda, pharmaceutical advertising is reasonable, legal and compliant. Enhance the concept of legal system, consciously operate in accordance with the law, to gain the trust of the community.
Fifth, consciously accept the supervision. Actively cooperate with the food and drug regulatory authorities in accordance with the implementation of the daily supervision of drug safety, special inspections, risk monitoring and emergency response, consciously accept the news media, the community's supervision. Efforts to improve the level of service for the healthy development of the pharmaceutical industry in Wuning to make due contributions.
Six, extensive publicity. Actively participate in the publicity of drug safety knowledge and lecture hall
activities, and strive to improve the quality and safety awareness of all staff, and seriously implement the "sold qualified products honor, sold shoddy products is shameful" concept, to provide scientific consumer information, advocate the rational use of medicines and healthy lifestyle behavior, and safeguard the legitimate rights and interests of drug operators and consumers.
Commitment of the enterprise (seal):
Commitment of the person (signature):
Year Month