For example, you want to do a "cybercafe", there are cultural departments, business sector, and fire, health, and so on the approval of the department, which is the most difficult to get the approval of the cultural sector.
How to get, this is the "Eight Immortals across the sea, each show their skills", but according to the formal channels to get the approval is harder than ever, and delayed time will be very long. Or find a gutsy middleman, pay a little money, take the wrong way to get an approval easier.
Question 2: What industry is the need for approval? 1. medical device sales, production (except for a class of medical devices) (District Drug Administration), drugs (District Drug Administration, Health Bureau) 2. books and newspapers, newspaper publications retail, printing (District Cultural Management, City Press and Publication Bureau) 3. audio-visual products sales (District Cultural Management) 4. liquor wholesale (District Liquor Monopoly Bureau) 5. food (District Health Bureau) 6. medical structure set up (District Culture and Student Affairs Bureau) 7. cigarettes Sales (Tobacco Monopoly Bureau) 8. Catering (District Environmental Protection Bureau, District Culture and Health Bureau, District Fire Department) 9. hotels, guest rooms (District Public Security Bureau, District Fire Department, District Health Bureau) 10. Plastic products, water-based paint production and processing (District Environmental Protection Bureau) 11. road transport, surface transport (Traffic Bureau) 12. automobile, motorcycle repair (Municipal Transportation Commission Maintenance Management Office) top 3. talent agency (District Personnel Bureau) 14. labor Labor service (District Labor Bureau) 15. scrap metal purchase (District Public Security Bureau, District Environmental Protection Bureau) 16. finished oil business, storage (Municipal Economic Commission, Public Security Bureau) 17. processing, sales, recycling of gold and silver (Municipal People's Bank of the Financial Services Division) 18. cultural relics (Cultural Relics Management Committee) 19. operating ballroom (Municipal Bureau of Culture, Cultural and Student Affairs Bureau, the Public Security Bureau, the Fire Services Department) 20. Chinese calligraphy (Municipal Bureau of Culture) 21. cafes, pubs (Health Department, Public Security Bureau) The city's liquor monopoly (health department, public security department, the city liquor monopoly) 22. Customs clearance business (General Administration of Customs) 23. Cement production (Municipal Construction Committee) 24. Air transportation sales agency business (Civil Aviation Administration of the Central and Southern China) 25. Cosmetic production (Municipal Health Bureau) 26. Engineering contracting (Municipal Construction Committee)
Specific questions you can ask me Oh, q 9 2 9 7 3 9 7 9 3 I am to do
Question 3: What is the company's approval number Approval number refers to the production of new drugs or drugs that have national standards, subject to the approval of the State Council drug supervision and management departments, and the approval of the document on the provisions of the drug's proprietary number. Drug production can only be done after the company has obtained the approval number for the drug. It is usually the company that produces the drug that applies for it.
Question 4: What is the approval number The production of new drugs or drugs that have national standards, subject to the approval of the State Council Drug Administration, and the approval of the document on the provisions of the drug's proprietary number, this number is called the drug approval number. Drug manufacturers can only produce the drug after obtaining the approval number.
Drug approval number format: State Drug Permit + 1 letter + 8 digits, trial production drug approval number format: State Drug Test + 1 letter + 8 digits.
Chemical drugs using the letter "H", Chinese medicine using the letter "Z", through the State Drug Administration to rectify the use of health care drugs using the letter "B", biological products using the letter "S". Biological products using the letter "S", in vitro chemical diagnostic reagents using the letter "T", the use of pharmaceutical excipients using the letter "F", the use of imported sub-packaged drugs using the letter "J". The first two digits of the original approval number for the source code, of which "10" on behalf of the original Ministry of Health-approved drugs, "20" 19 "," on behalf of January 1, 2002 Prior to the State Food and Drug Administration approved drugs, other provinces using the first two administrative code, the original provincial health administrative departments approved drugs. The third and fourth for the exchange of the approval number of the year of the year number of the last two digits of the A.D., but from the Ministry of Health and the State Drug Administration of the approval number is still the use of the original number of the last two digits of the number of the year number. Figures 5 to 8 for the order of the number.
Question 5: What is the role of the approval number? Approval number: the production of new drugs or national standards for drugs, subject to the approval of the State Council drug supervision and management department, and the approval of the document on the provisions of the drug's proprietary number, this number is called the drug approval number. Drug manufacturers can only produce the drug after obtaining the drug approval number.
Drug approval number format: State Drug Permit + 1 letter + 8 digits, trial production drug approval number format: State Drug Test + 1 letter + 8 digits.
Just like the human identity card, according to the approval number can accurately find the drug!
Question 6: What is the approval number of health care products production of new drugs or drugs that have national standards, subject to the approval of the State Council Drug Administration, and the approval of the document on the provisions of the drug's proprietary number, this number is called the drug approval number. Drug manufacturers can only produce the drug after obtaining the approval number.
At present, there are two types of health food approval number:
1, "health food and health word" to the Ministry of Health website query, query the authenticity of the health care products specific method is as follows: open the official website of the Ministry of Health, click on the right side of the website "data query "column in the" health-related products query "in the pop-up page click" health food approval bulletin catalog "and then according to the product's approval of the number of years to choose the query can be.
2, "State Food and Health" to the State Food and Drug Administration website query, query the authenticity of the health care products specific methods are as follows: open the official website of the State Food and Drug Administration, click on the right side of the website "basic data query" column in the "health food", in the pop-up page click on "health food", and then enter the product information can be queried (it is best to enter the name of the product).
Question 7: Batch number and approval number Batch number is to indicate that the product is out of the warehouse to determine the batch, like a person's birthday, January 1, 09 born in the product out of the warehouse to see, for example, January 1, 09 out of the warehouse, and so on
Approval number is to indicate that the relevant state authority agreed to the approval of the relevant acts of an enterprise, like a stamp
The "Drug Registration Approval", "Health Food" pop-up page, click on the "Health Food", and then enter the relevant information about the product to query (it is best to enter the name of the product). Question 8: What is the difference between "Drug Registration Approval" and "New Drug Certificate and Production Approval"? Drug Registration Approval" is the State Drug Administration approved a drug manufacturer to produce the species, issued "approval number" of the statutory documents, in layman's terms, that is, the drug's "birth certificate", that is, usually said to be "production approval". "Production authorization". The same drug, if the policy permits, there may be more than one pharmaceutical company to apply for registration, after the state review qualified, will be approved to a number of pharmaceutical companies to produce, so the pharmaceutical companies will have the drug "Drug Registration Approval" just "approval number" is not the same. New Drug Certificate" is a legal ownership document issued by the State Drug Administration to the applicant of a new drug (the organization that submits the application for drug registration, assumes the corresponding legal responsibility, and holds the document of drug approval after the approval of the application) through a comprehensive review of the information declared for the registration of the new drug, and also the legal ownership document of the applicant, and also the legal ownership document of the applicant, after the approval of the application. The legal ownership documents of the new drug are also issued to the new drug's "Drug Registration Approval Certificate". The enterprise that holds the Certificate of New Drug and can produce the drug is the only one in the country within the time period stipulated in the Measures for the Administration of Drug Registration. The form of approval document such as the New Drug Certificate and Production Approval has not been seen yet. According to regulations, the "new drug certificate" is transferable, and "production approval" is not transferable.
Question 9: How do I get the approval for API production? This procedure is very troublesome, first of all, you have to study, research the synthesis of raw materials, testing, detailed research after the composition of the declaration of information to the State Drug Administration to declare the State Drug Administration, the State Drug Administration Evaluation Center that your research in line with the provisions of the production of raw materials, safe, effective, stable, will be issued to you after a production approval. Conditions nail must be declared by the manufacturer holding a GMP certificate of authentication. There are many relevant situations, you can check the relevant provisions of the Drug Administration Law, or you can contact me. I am now doing drug research and development. [email protected]