Urgently need all the information of pharmacy retail GSP on site acceptance, thank you

This is very simple, as long as it is done in accordance with the GSP requirements, the principle of five separations (separation of drugs and non-drugs, separation of oral and external use, separation of prescriptions and non-prescriptions, separation of easy flavors, separation of toxicity) safety (fireproof, waterproof and insect proof, drug display, etc.) pharmacy hanging documents (drug business licenses, etc. can not be remembered) employee files (retail pharmacy education at least high school or above, health certificate, copy of ID card, etc.) is mainly the management of those file bags (prescription registration, employee files, temperature and humidity records, Ephedrine-containing drug registration, Chinese medicine decoction piece purchase registration, quality inspection, Western medicine commodity column, quality inspection, etc.) retail pharmacy quality administrator on duty, pharmacist on duty, each employee is familiar with GSP knowledge, can answer questions, the most important thing is to see if your company gives the red envelope to the Food and Drug Administration! I haven't worked in a pharmaceutical company for many years, and I can't remember it clearly, I hope it can help you!

This is everywhere on the Internet, I posted it in a forum, I hope to help you with the information of the violent store, it is a pity not to accept (the way of business and GSP full set) I hope to help you.

six categories of retail files; Management responsibilities, personnel training, facilities and equipment, purchase acceptance, display maintenance, sales and service.

Depending on the store, the file production is different. The certification of the new store is different from the expiration certification of the old store, and the key is to standardize the operation. The preparation work is divided into hardware preparation, software preparation and business association preparation.

This is very troublesome, no one helps you, it is difficult to prepare by yourself, I also asked other experienced people to help me prepare, I have been preparing for 2 months.

You may ask something, but these are some of the things that are often asked:

1. The supervisor of the company gives a brief introduction to the company's situation;

2. The person in charge of quality management, the setting of the quality management organization, and the introduction;

3. The person in charge of the quality management department briefly asks about the basic knowledge of quality management;

4. How to carry out the acceptance of the acceptance personnel, the place is in the first place, the main project content of the acceptance drug, and the on-site demonstration;

5. How to carry out maintenance by maintenance personnel, the main content, how to determine the key maintenance varieties, the determination of the maintenance cycle, and on-site demonstration;

6. Acceptance and maintenance personnel operate and accept maintenance instruments and facilities and equipment on site, and the maintenance cycle of facilities and equipment;

7. Some basic regulations and operating procedures for drug storage of warehouse custodians;

8. Assessment of quality management system;

9. Purchaser, whether the formulation of the procurement plan requires the signature of the quality control personnel;

10. Whether the licensed pharmacist is on the job and inquire about the financial salary schedule;

11. Online verification, supplier qualification, online query of drug registration information, on-site operation;

12. Review the qualifications of the other party when selling;

13. Matters related to special management drugs;

14. Implementation of online supervision.

The main reason for this is the transition between the new revised GSP and the old GSP

According to the notice of the State Food and Drug Administration on the implementation of the newly revised "Good Practice for Drug Operation" (Food and Drug Administration Yaohua Jian 2013 No. 32), before December 31, 2015, all drug business enterprises must meet the requirements of the newly revised drug GSP, regardless of whether their "Drug Business License" and "Drug Business Quality Management Practice Certification Certificate" have expired. Since January 1, 2016, those who have not met the requirements of the newly revised drug GSP shall not continue to engage in drug business activities.

The pharmacy should expire around August 2014, but the certification of the newly revised GSP has not yet been comprehensive, and the local drug regulatory department has to renew the "Drug Business License" according to the original GSP certification standards and license renewal standards, but it cannot violate the national regulations on the implementation of the newly revised GSP. Therefore, only the validity period of the pharmacy license is marked until December 31, 2015 (the question should be a clerical error), which means that the pharmacy must also apply for and pass the newly revised GSP certification before December 31, 2015, and the local drug regulatory department will issue a "drug business license" valid for 5 years.