Pharmacy Commitment 1 Dear leaders and colleagues of various operating enterprises,
Drug safety is the most realistic, concerned and direct interest of the people. It is the social responsibility and obligation of every pharmaceutical enterprise to improve the construction of enterprise spiritual civilization, advocate the management consciousness and concept of civilization, law-abiding and honesty, effectively ensure the safe and effective use of drugs by the people, and strive to become a "hundred assured pharmacies" in Xiaoshan District. Food and drug quality and safety are 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 the drug supervision and administration department, our company has undergone great changes in management and the quality of its employees has been improved. Now, it is to establish a good image of pharmaceutical trading enterprises that are honest and trustworthy, fair trade, serve the masses and contribute to society. Hangzhou Xiaoshan Tongchuntang Pharmaceutical Retail Co., Ltd. and 43 pharmaceutical chain stores take "100 assured pharmacies" as the implementation standard to ensure that the medicines we provide will reassure and be safe for the people, and solemnly promise to leaders, enterprise colleagues and people in the whole region as follows:
First, study hard, fully implement the Drug Administration Law, the Regulations for the Implementation of the Drug Administration Law, and the Standards for the Quality Control of Drugs, and abide by the law and be strict with yourself. Buy drugs from legal channels, ensure the consistency of tickets and goods, and never deal in counterfeit and inferior drugs.
Second, firmly establish the quality awareness of drug quality first and being responsible for people's health, engage in drug business activities in strict accordance with the requirements of the "Drug Quality Management Standards" and provide safe and qualified drugs for the masses.
Third, consciously maintain the order of drug market operation, establish the marketing concept of fair competition, honesty and trustworthiness, and introduce the characteristics of drugs and safe drug use to consumers scientifically and realistically.
Knowledge, resolutely oppose unfair competition.
Four, pharmaceutical practitioners should consciously abide by professional ethics, love their jobs, strive for first-class service, create a good environment for drug purchase, serve consumers with sincerity and love, establish a corporate image, and create a "rest assured pharmacy".
Five, in strict accordance with the provisions of the national "Advertising Law" and "Drug Administration Law", do not make false advertisements, and do not mislead and deceive consumers in any form. Strictly implement the national drug price policy, clearly mark the price, and be childlike.
Six, the illegal activities in drug business activities should be brave enough to report, timely report the adverse reactions of drugs and medical devices found, maintain a good order of drug circulation, and ensure the safety and confidence of the people in drug use.
It is our responsibility to build the integrity and safety of drugs and reassure people, actively participate in the activities of "assured pharmacies", establish enterprises with integrity, promote development with integrity, create more value and return more to society. Let's join hands, start from me and start from now. At the same time, I hope to join hands with other pharmaceutical enterprises in the region to strengthen the publicity of corporate civilization and integrity, and make new contributions to building a harmonious and honest Xiaoshan! .
Hangzhou Xiaoshan tongchuntang medicine retail co., ltd
20xx.04.26
2××× Municipal US Food and Drug Administration:
I understand the relevant requirements of the Notice of the State Food and Drug Administration on Electronic Supervision of Essential Drugs (No.[20xx] 194 of the US Food and Drug Administration):
1. The bid-winning enterprises that produce basic drug varieties should join the drug electronic supervision network before March 3 1 20xx. Before the basic drug varieties leave the factory, the production enterprises must print (affix) the drug electronic supervision code with uniform identification on the listed products in accordance with the regulations, and collect and submit the data through the supervision network.
Two, 20xx April 1 day, the varieties listed in the list of essential drugs, not into the network and not unified identification of drug supervision code, shall not participate in the bidding and procurement of essential drugs.
I solemnly promise not to produce essential drugs for the time being (or not to participate in centralized bidding and purchasing of essential drugs). Before production (or before participating in centralized bidding and purchasing), complete all related work such as process verification and electronic supervision of essential drugs to ensure the quality of essential drugs production, and collect and submit data through the electronic supervision network of drugs. Voluntary acceptance of supervision and inspection by drug supervision and administration departments at all levels.
Commitment (signed by the legal representative of the enterprise):
(official seal)
date month year
This undertaking is made in triplicate. A copy to the provincial bureau, the city (prefecture) bureau and the commitment enterprise each hold a copy.
Pharmaceutical Commitment 3 I. General situation of enterprises
Established in March of 20xx, this enterprise is an individual drug retail enterprise. Enterprises take GSP as the criterion to compile and improve the enterprise quality management system.
At present, the company has 4 employees, including 2 pharmacists, pharmacists 1 person, and pharmaceutical professionals account for 100% of the total number. The allocation of pharmaceutical technicians can meet the requirements of quality management in pharmaceutical enterprises.
Second, the personnel organization of GSP organization
The enterprise shall set the person in charge, purchasing, maintenance and warehouse keeper as XX; The quality director is XXX；; The quality manager and inspector are XXX；; The examiner is XXXX and the salesperson is XXX and XXX, which defines the quality responsibilities of full-time quality personnel.
Three. Personnel and training
In order to continuously improve the professional and technical quality of all employees, a study and training plan has been formulated, and all employees are regularly organized to study drug management laws and regulations and professional and technical knowledge, and the assessment is conducted once every six months, and training files are established.
Four. Facilities and equipment
According to the requirements of the new GSP, the enterprise is equipped with computers and software for managing the purchase, sale and storage of drugs that meet the relevant management requirements, and is equipped with temperature and humidity detection equipment in the business place. Now it is equipped with a thermometer and an air conditioner. And equipped with rat-proof, insect-proof and fire-proof equipment. The business premises are clean and bright, and the business shelves and counters are complete.
Five, drug procurement, acceptance management
According to the requirements of the Drug Administration Law, the Quality Management Standard for Pharmaceutical Trading and other relevant laws and regulations, the quality and legal qualification of purchased drugs were reviewed, and the GSP certificate of drugs, the Pharmaceutical Trading License (Wholesale) and a copy of the business license stamped with the official seal of the enterprise were obtained. The power of attorney shall specify the scope and duration of authorization; A copy of the ID card of the drug salesman; To purchase imported drugs, ask the supplier for a copy of the registration certificate of imported drugs and the inspection report of imported drugs, and affix the original seal of the supplier's quality management agency; Imported drugs should have Chinese instructions. The audit system shall be implemented for enterprises that declare for the first time and drugs that declare for the first time. The enterprise has established a drug purchase ledger to record the drug purchase truly and completely, so that the tickets, accounts and goods are consistent, and then input them into the computer according to relevant procedures to do all the basic work well.
Acceptance management: The acceptance personnel shall, according to the original vouchers and tax receipts, check and accept the purchased drugs in batches in strict accordance with relevant regulations, and record them. Mainly check whether the accepted drugs meet the corresponding appearance quality standards. (1) Whether the outer packaging is firm and dry; Whether the seal and seal are damaged; Does the outer package indicate the general name, specification, manufacturer, approval number, registered trademark, batch number and expiration date? Whether the specific storage and transportation marks meet the requirements of drug packaging. (2) Whether there is a product certificate for each inner package, whether the container is reasonable, whether there is any damage, whether the seal is tight, whether the packaging handwriting is clear, and the product name, specification and batch number shall not be omitted; Bottle labels should be affixed securely. (3) The generic name, ingredients, specifications, manufacturer's name, approval number, production batch number, production date and expiration date of the drug are clearly printed on the drug label instructions. Labels or instructions should also include indications or functional indications, usage and dosage, contraindications, adverse reactions, precautions and storage conditions. (4) The name, main components and registration number are indicated on the label of the imported drugs, and there is a Chinese manual, with the registration certificate of the imported drugs, the approval number of the imported medicinal materials and the inspection report of the imported drugs, and a copy of the red seal of the supplier's quality management institution is affixed. Collect adverse drug reactions in time and report them to the drug supervision department immediately.
Six, drug storage, maintenance and display (retail) management.
At the beginning of our enterprise's establishment, we created a storage and exhibition environment in strict accordance with GSP requirements, and decorated the business area according to the latest standards of the Municipal Bureau to make the business place spacious and bright. Shopping is convenient and the signs are eye-catching. According to the business situation and GSP requirements, drugs are classified. According to the performance and nature of drugs, the warehouse is divided into areas to be inspected (yellow), mixed areas (green), unqualified areas (red) and returned areas (yellow), so that drugs and non-drugs, external drugs and internal drugs can be stored separately, which is convenient for operation and prevents errors and pollution incidents. Shelves, greenhouse thermometers, light-proof facilities (curtains) and rat-proof facilities (door seals) have been added to meet the requirements of "seven precautions" (dustproof, insect-proof, bird-proof, rat-proof, moisture-proof, mildew-proof and pollution-proof). Install lighting equipment that meets the lighting requirements. Air conditioners are installed in commercial areas to ensure proper air humidity and temperature. Manage according to the Management System of Drug Storage, Maintenance and Display of our store. For example, drugs and non-drugs are displayed separately, over-the-counter drugs and prescription drugs are displayed separately, and internal drugs and external drugs are displayed separately. Special preparations, including ephedra preparations, are displayed at the counter, and warning slogans are marked. The counter in the disassembly area is equipped with corresponding disassembly tools. In addition, measure the temperature and humidity of the business area and warehouse every morning and afternoon, and take timely measures to adjust if it does not meet the requirements; Check the maintenance of drugs in stock and display regularly every month, and record as required. These measures can ensure the storage quality of drugs.
Seven, sales and after-sales service
In order to provide consumers with reliable drugs and high-quality services, enterprises conduct business training and assessment for salespersons engaged in drug retail. Drug sales, for the drugs purchased by customers, after verification, the drugs will be handed over to customers, and sales vouchers will be issued, and at the same time, the medication methods and taboos will be explained to customers in detail; Express the service convention in the business place, announce the supervision telephone number, and set up a customer suggestion book. Solve customers' comments and complaints in time, take seriously the drug quality problems reflected by customers, record them in detail and deal with them in time.
Eight, computer software system
Computer system is a famous big company in China. Relevant modules meet the application requirements of the new GSP, automatically remind the inventory every day, and urge the sales of products near the shelf life every month. Expired enterprises and expired drugs can automatically restrict related procurement, acceptance and sales activities, and hemp-containing preparations can automatically restrict sales with their registered names and ID cards.
Nine. self-check
Our pharmacy has set up a self-inspection team headed by XXX, with the quality director as the core, to conduct self-inspection and rectification on the implementation of GSP management in our store:
First, scientifically summarize and sort out relevant archival records; The second is to fill in the sales label instructions on the shelves; The third is to clean the storefront again; The fourth is to further check and standardize classified management. Through self-examination and self-correction activities, the management level of GSP has been further improved.
Through GSP self-inspection, we believe that the standard requirements have been initially met, and now we apply for certification. Welcome the leaders to check and guide.
In order to effectively strengthen the quality management of pharmaceutical retail (chain) enterprises, promote law-abiding, standardized, honest and civilized operation, and promote the creation of a national civilized city, we hereby make the following commitments:
1. Strictly abide by the Code for Pharmaceutical Trading Enterprises to Establish a National Civilized City formulated by the US Food and Drug Administration, implement thirteen requirements in four aspects: beautiful environment, excellent management, quality and safety, and excellent service, abide by the "12 noes" commitment, carry out the campaign of "all stores in the province are free of counterfeit drugs" in depth, solidly promote the creation of a national civilized city, and ensure that the national evaluation team does not lose points in inspection.
Two, in strict accordance with the requirements of the national "Regulations on the Administration of Drug Classification of the US Food and Drug Administration", prescription drugs are sold by prescription. When selling prescription drugs, they must be examined and signed by licensed pharmacists or other qualified pharmaceutical technicians before they can be sold.
Third, strictly implement the relevant regulations of the state on the management of compound preparations of special drugs (including compound preparations containing ephedrine, compound oral solutions containing codeine, compound diphenoxylate tablets and compound licorice tablets), and each sale shall not exceed two minimum packages. When they find abnormal purchases, they should immediately report to the US Food and Drug Administration to prevent abuse.
Fourth, strictly implement the responsibility of "the first responsible person of the enterprise", strengthen the implementation of the "Quality Management Standard for Pharmaceutical Trading", strengthen the training, education and management of enterprise employees, ensure that the person in charge of pharmaceutical quality is on the job, and consciously create and maintain a good pharmaceutical trading order.
Enterprise name: Linzhi Hengkang Fair-price Pharmacy
Commitment:
Month, Day, 2 15
US Food and Drug Administration in Xiaoshan District, Hangzhou:
I hereby entrust Pei Feifei to apply for administrative license on behalf of me (unit).
Authorization: submit all materials related to this administrative license and sign for it.
Various certificates and licenses in the process of administrative licensing.
The power of attorney is valid from 20xx 10 year 10 month/0 day to the license documents and certificates.
According to the receipt.
Customer (unit):
Legal representative (person in charge): (signature)
date month year
Pharmacy Commitment Article 5 The relevant materials of the application for signing the basic medical insurance for provincial designated retail pharmacies submitted by this unit are true, legal and effective. If it is untrue, I am willing to bear all responsibilities and consequences.
Applicant Wang Wenbin (signature), 20xx65438+February 2.
Applicant: Minhou No.1 Branch of Le Kang Pharmacy, Taijiang District, Fuzhou.
(Signature) 20xx65438+February 2.
Pharmacy promises Article 6 to xxx pharmacy leaders:
In my nearly three years' work, I have no bad record of violating laws and regulations, violating regulations or canceling the contract because of personal application, and not defrauding the bid. During my work, no pharmacy was in the punishment stage of being ordered to close down, having its property taken over or frozen, or having its bidding activities suspended.
I hereby promise.
Commitment (signature):
Date: year month
7 The pharmacy of the US Food and Drug Administration in Xiaoshan District, Hangzhou promises that:
I hereby entrust Pei Feifei to apply for administrative license on behalf of me (unit).
Authorization: submit all materials related to this administrative license, and sign for all kinds of documents and licenses in the process of handling administrative license.
The power of attorney is valid from 20xx 10 to 0 1 year 10 months until the license document and license are signed.
Customer (unit):
Legal representative (person in charge): (signature)
date month year
8 The pharmacy of the US Food and Drug Administration in Xiaoshan District, Hangzhou promises:
I hereby entrust Pei Feifei to apply for administrative license on behalf of me (unit).
Authorization: submit all materials related to this administrative license, and sign for all kinds of documents and licenses in the process of handling administrative license.
The power of attorney is valid from 20xx 10 to 0 1 year 10 months until the license document and license are signed.
Customer (unit):
Legal representative (person in charge): (signature)
date month year
Note: If the client is an individual, the client should sign his name, date and fingerprint; If the client is an enterprise, the legal representative or responsible person shall sign the name and date and affix the official seal. Attach a copy of the customer's ID card.
According to the requirements of relevant laws, regulations and rules and regulations, such as the Drug Administration Law, the Quality Management Standard for Pharmaceutical Trading, etc., the pharmacy promises to ensure that the drugs handled by our store are' qualified in quality and safe to use' in Article 9, and conduct self-inspection on the relevant links of pharmaceutical trading in our store. The self-inspection is as follows:
I. Basic information of the enterprise
Person in charge of the enterprise: xxxx, graduated from xxxx Department, with the title of professional pharmacist. Business address: xxxxx, business scope: biochemical products, Chinese herbal medicines, Chinese herbal pieces, biological products (excluding preventive biological products), Chinese patent medicines, chemical preparations and antibiotic preparations. Economic nature: chain stores. The enterprise tenet of "survival by quality, development by honesty" follows the moral principles of mutual benefit, common development, honesty first and management according to law.
Second, the staffing situation:
According to the requirements of laws, regulations and rules related to drug management, our store has established xxx as the main person in charge; Person in charge of quality and person in charge of quality organization: quality leading group with xxx as the unit, and acceptance maintenance personnel: XXX; Medical shopping guide: xxx. Store * * * has xxx employees.
Three. Management personnel training and assessment system and regular physical examination system for each post.
1. The person in charge of store quality management shall make an annual training plan every year according to the training requirements of enterprise employees on laws and regulations related to drug management, train store employees on laws and regulations and professional knowledge as planned, and establish training files at the same time.
2. In order to ensure the quality and safety of the drugs handled by the store, the business personnel and the person in charge of quality who are in direct contact with the drugs shall have a health examination at least once a year. Only employees who pass the medical examination can continue to work, and employees who fail the medical examination must immediately stop working and be transferred from their posts. And establish health records. Four. Overview of quality management system documents
In order to implement the management of the new GSP certification, we have formulated the following quality management system documents:
1, store drug procurement and acceptance quality management system
2. Drug display management system in shopping malls
3, store drug sales and prescription deployment management system
4, the mall drug removal drug management system
5, shopping mall drug maintenance inspection management system
6, health and personnel health management system
7, store service quality management norms
8, adverse drug reaction reporting system
9, unqualified drug management system
10, quality management inspection and assessment system
1 1, the management system for storing Chinese herbal pieces
12, cold storage drug management system
13, computer management system
Verb (abbreviation for verb) Facilities and equipment:
1. According to the relevant regulations and requirements for dealing in drugs, the business area of the store is 1 10 square meters, and the store is strictly managed by districts with obvious signs.
2. The store is clean, tidy, dry and well ventilated, and there is no pollution source around. The store is equipped with facilities and equipment suitable for drug storage: air conditioners, shelves, containers, Chinese medicine cabinets, medicine disassembling cabinets, medicine disassembling tools, processing tools, computers, software, mousetraps, fire extinguishers, freezers, direct-reading hygrometers, scales and dark curtains.
Overview of intransitive verbs computer system
With the implementation of GSP certification, in order to better manage and sell, we upgraded the computer software, compiled a new record account and record form according to the new version of GSP certification software, re-compiled the quality management system documents according to the requirements of GSP, established a perfect quality management system and working procedures, and incorporated all the work into modern microcomputer management, effectively ensuring the standardized operation of store work.
Seven, drug procurement, acceptance, storage, maintenance, sales and other aspects of the management and operation procedures.
1, drug procurement
Drug procurement shall be carried out in strict accordance with the quality management system of pharmacies, strengthen the audit of supplier quality assurance system, require suppliers to provide copies of Drug Business License and Business License with official seals, establish supplier files, strengthen the qualification audit of supplier drug sales personnel, and sign quality assurance agreements with suppliers; When purchasing imported drugs, suppliers are required to provide a copy of the Registration Certificate of Imported Drugs or the Registration Certificate of Pharmaceutical Products and the Inspection Report of Imported Drugs stamped with the original seal of the supplier's quality management organization, so as to ensure good quality from the source.
2. Drug acceptance.
We check and accept the appearance, shape, packaging and label of drugs in strict accordance with the corresponding laws and regulations, quality terms and quality standards of the contract, and resolutely reject those that do not meet the requirements.
3, standardize the management of drug display
In accordance with the requirements of GSP, pharmacies standardize the management of drug display, so as to place drugs according to their purposes. At the same time, drugs are stored separately from non-drugs, drugs for internal use and external use, and drugs that are easy to smell, and prescription drugs and over-the-counter drugs are stored in separate cabinets, with obvious and clear labels. Check the drugs on display every month and record them truthfully.
4. Pay attention to the maintenance of drugs.
I store and display drugs reasonably according to the quality management system of pharmacies and the storage conditions of drugs. I record the temperature and humidity of the business premises on time every morning and afternoon, and take timely control measures when the temperature and humidity do not meet the requirements of drug storage. At the same time, the general drugs in stock are inspected quarterly, and the key maintenance varieties are inspected monthly. The maintenance files of key maintenance varieties have also been established, and the maintenance records are true, perfect and standardized.
5. Do a good job in drug sales.
In order to standardize the behavior of the drug trading industry and provide consumers with reliable drugs and quality services, prescription drugs are audited by prescription, and other drug salesmen can insist on asking questions to achieve "three questions", that is, asking about the condition, gender and age, that is, explaining the administration method, dosage and precautions, and handing over according to the name, specification, quantity and price of the drugs purchased by customers. And provide consulting services to guide customers to use drugs safely and reasonably.
6. Management of returned drugs
1. The returned drugs shall be kept by a special person, stored in a special area and recorded in a special account.
2, all returned drugs should be re acceptance, a clear conclusion, qualified rear can sell.
3. All unqualified drugs or drugs with problems should be contacted with suppliers in time and properly handled.
4. The returned drugs with problems should be stored in the return area or waiting area.
5. The return record is complete, accurate and standardized, with complete procedures and signatures, and kept as required.
7. Complaint handling
Pharmacies clearly state the service convention in the business hall, announce the supervision telephone number and set up a customer suggestion book; Seriously deal with customers' opinions and take effective improvement measures in time. Records of quality inquiries, complaints, drug returns and services provided are true and complete, and should be properly kept.
8, adverse drug reaction reporting system
1, with clear concept, clear responsibilities and standardized process.
2. Effectively collect information on adverse drug reactions.
3, found that adverse drug reactions reported in a timely manner.
4. Records are complete, accurate and standardized.
Eight, bill management system
1, strengthen the management of bills, put an end to the loss of bills, whoever takes the bill will be responsible, and the economic losses caused by the loss of bills will be compensated by the responsible person.
2. For the settlement of non-compliant bill materials, the Finance Department has the right to refuse to use informal bills for reimbursement. () After receiving your notice, Li San Pharmaceutical Company held a meeting in time to convey the layout work, and asked my subordinate enterprises to carry out self-examination and self-correction within their own departments, conduct strict self-examination in accordance with the laws of the US Food and Drug Administration and the regulations of GSP management, and write self-examination reports according to their respective conditions. As required, Lisan No.5 Pharmaceutical Company conducted a self-inspection, and now the results of the self-inspection are reported as follows:
After we received the notice, all the staff took action, and under the leadership of the head of our department, conducted a comprehensive inspection of the interior of the store, which took a day. Finally, we summarized the inspection results and found the following problems:
1, the store reminds and warns customers that the brand is aging and loses its aesthetic feeling. We made changes in time, and now we have replaced new warning signs.
2. The overall hygiene of pharmacy is OK, but some dead corners are not clean enough. For example, the bottom compartment of each counter is not thoroughly cleaned. On the spot, the salesman was criticized and educated and asked to correct it in the future.
3. Recently, drugs were not paid attention to in time, so that customers found the problem only after seeing it. We must check the monitor carefully 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 found some problems in our work. We must take this inspection as an opportunity, make serious rectification, work hard, do a better job in the operation of our store, satisfy customers, and let the people really use medicines that are at ease.
3. The receipt and cancellation of bills must go through the handover registration and receipt procedures according to regulations.
4. The bills are effectively controlled, classified and filed, and properly kept.
Nine, the main problems and corrective measures
In order to better implement GSP, our store conducted a comprehensive self-examination through reporting, field visits, consulting materials, investigation and inquiry. Through self-examination, we think that it has basically reached the requirements of "Quality Management Standards for Pharmaceutical Trading" and its implementation rules, but there are still gaps in some aspects: (for example, pharmacy staff are not aware of their business and the service quality is not standardized enough).
In view of the above problems, our store has carried out serious analysis and research, and formulated measures to require all post personnel to strengthen their awareness of business learning, strive to master various business knowledge in a short time, and strive to improve service quality. At the same time, we will take this GSP certification as an opportunity to further enhance the awareness of quality management, intensify quality management, constantly strengthen and improve the hardware construction and software management of stores, and strive to gradually modernize, standardize and institutionalize quality management to ensure the drug safety of the general public.
Pharmacy promises 10 first, implement quality responsibility. Conscientiously implement the Drug Administration Law, the Regulations for the Implementation of the Drug Administration Law and a series of national drug-related laws and regulations, earnestly fulfill the obligations of the first person responsible for drug safety, further establish and improve the drug quality and safety guarantee system, strengthen daily quality management with a responsible attitude towards public health, and ensure drug safety.
Second, strict self-discipline. Never sell unqualified medicinal capsules and other medicinal excipients; Drugs and medicinal hollow capsules sold must be inspected by drug inspection institutions before they can be sold.
Third, strengthen safety management. Further establish and improve the drug safety guarantee mechanism, fully implement the quality management norms of drug business, strive to improve the standardized management level, increase the intensity of adverse drug reaction detection reports, eliminate drug safety hazards, and prevent drug safety accidents.
Fourth, adhere to honesty and law-abiding. Based on honesty, firmly establish a sense of honesty, value contracts and keep promises, do not make false propaganda, and the advertisements for medical devices are reasonable, legal and compliant. Strengthen the concept of legal system, consciously operate according to law, and win the trust of the society.
Fifth, consciously accept supervision. Actively cooperate with the daily supervision, special inspection and risk monitoring emergency disposal of drug safety implemented by the food and drug supervision department according to law, and consciously accept the supervision of the news media and all sectors of society. Strive to improve the service level and make due contributions to the healthy development of Wuning Pharmaceutical.
Sixth, carry out extensive publicity. Actively participate in the publicity and lecture hall of drug safety science knowledge.
Activities, efforts 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", provide scientific consumption information, advocate rational drug use and healthy life behavior, and safeguard the legitimate rights and interests of drug dealers and consumers.
Commitment enterprise (seal):
Commitment (signature):
date month year