For example, to run an "Internet cafe", it needs the approval of the cultural department, the industrial and commercial department, the fire department and the health department. Among them, the most difficult thing is the approval of the cultural department.
How can I get it? This is "eight immortals crossing the sea, each showing his magical powers", but it is difficult to get approval according to formal channels and it takes a long time. It is easier to find a courageous middleman, pay some money and get approval by improper means.
Question 2: Which industries need approval? 1. Sales and production of medical devices (except Class I medical devices) (FDA District) and drugs (FDA District and Health Bureau) 2. Books, newspapers and periodicals retail and printing (District Cultural Management Office, Municipal Press and Publication Bureau) 3. Sales of audio-visual products (District Cultural Management Office) 4. Liquor Wholesale (District Liquor Monopoly Bureau) 5. Food (District Health Bureau) 6. Establishment of medical institutions (District Culture and Health Bureau) 7. Tobacco Sales (Tobacco Monopoly Bureau) 8. Catering (District Environmental Protection Bureau, District Cultural and Health Bureau, District Fire Bureau) 9. Production and processing of water-based paints in hotel rooms (District Public Security Bureau and District Fire Bureau) 1 1. Road transportation, surface transportation (Transportation Bureau) 12. Automobile and motorcycle maintenance (Municipal Communications Commission Maintenance Management Office) 3. Talent Agency (District Personnel Bureau) 14. Labor Service (District Labor Bureau) 15. Warehousing (Municipal Economic Commission, Public Security Bureau) 17. Gold and silver processing, sales and recycling (Financial Office of the People's Bank of China) 18. Cultural Relics Management (Cultural Relics Management Committee) 19. There are 20 business dance halls (Municipal Bureau of Culture, Wen Sheng Bureau, Public Security Bureau and Fire Bureau). China Traditional Calligraphy and Painting (Municipal Bureau of Culture) and Municipal Liquor Monopoly Bureau) 22. Customs declaration business (General Administration of Customs) 23. Cement Production (Municipal Construction Committee) 24. Air transport sales agency business (Central South Administration of Civil Aviation) 25. Cosmetic production (Municipal Health Bureau) 26. Project contracting (Municipal Construction Committee)
You can ask me specific questions. Q 9 2 9 7 3 9 7 9 3 I am an industrial and commercial agent.
Question 3: What is the approval number of the company? The approval number refers to the production of new drugs or drugs with national standards, which must be approved by the State Council Drug Administration, and the patent number of the drug must be stated in the approval document. A pharmaceutical production enterprise can produce the drug only after obtaining the drug approval number. Generally, companies that produce drugs will apply.
Question 4: What is the production approval number of new drugs or drugs with national standards? It must be approved by the drug supervision and administration department of the State Council, and the proprietary number of the drug is specified in the approval document, which is called the drug approval number. A pharmaceutical production enterprise can produce the drug only after obtaining the drug approval number.
The format of drug approval document number: National Medicine Zhunzi+1 digit letter +8 digits, and the format of trial production drug approval document number: National Medicine Shenzi+1 digit letter +8 digits.
The letter "H" stands for chemicals, the letter "Z" stands for traditional Chinese medicine, the letter "B" stands for health care drugs rectified by the State Administration of Pharmaceutical Products, the letter "S" stands for biological products, the letter "T" stands for in vitro chemical diagnostic reagents, the letter "F" stands for pharmaceutical excipients and the letter "J" stands for imported sub-packaged drugs. Numbers 1 and 2 are the source codes of the original approval number, where "10" represents the drugs approved by the former Ministry of Health, "20" 1 9 "and"1"represent the drugs approved by the US Food and Drug Administration before June 2002, and others use the first two digits of the provincial administrative division code. The third and fourth digits are the last two digits of the renewal year of the approval number, but the approval numbers from the Ministry of Health and the State Administration of Pharmaceutical Products still use the last two digits of the original number. Numbers 5 to 8 are serial numbers.
Question 5: What is the function of the approval number? Approval number: The production of new drugs or drugs with national standards must be approved by the drug supervision and administration department of the State Council. The approval number contains the proprietary number of the drug, which is called the drug approval number. A pharmaceutical production enterprise can produce the drug only after obtaining the drug approval number.
The format of drug approval document number: National Medicine Zhunzi+1 digit letter +8 digits, and the format of trial production drug approval document number: National Medicine Shenzi+1 digit letter +8 digits.
Just like a person's ID card, you can find the medicine accurately according to the approval number!
Question 6: The approval number of health care products refers to the production of new drugs or drugs with national standards, which must be approved by the drug supervision and administration department of the State Council, and the exclusive number of the drug is specified in the approval document, which is called the drug approval number. A pharmaceutical production enterprise can produce the drug only after obtaining the drug approval number.
At present, there are two approval numbers for health food:
1, "Wei Shi Jian Zi" went to the website of the Ministry of Health to check the authenticity of this health care product. The specific method is as follows: Open the official website of the Ministry of Health, click "Health-related Product Inquiry" in the column of "Data Inquiry" on the right side of the website, click "Catalogue of Health Food Approval Announcement" in the pop-up page, and then select the inquiry according to the product approval years.
2. Search the word "National Food and Drug Administration" on the website of the US Food and Drug Administration. The specific method to query the authenticity of this health care product is as follows: Open the official website of the US Food and Drug Administration, click "Health Food" in the column of "Basic Information Query" on the right side of the website, click "Health Food" in the pop-up page, and then enter the relevant information of the product to query (it is best to enter the product name).
Question 7: The batch number and approval number indicate the batch number determined after the product leaves the warehouse, just like a person's birthday. Born on June 65438+1 October 1 day in 2009, the products were delivered from the warehouse on June 65438+1October/day in 2009, and so on.
The approval number means that the relevant national authorities agree to approve the relevant behavior of the enterprise, just like stamping.
Question 8: What is the difference between drug registration approval and new drug certificate and production approval? The drug registration approval number is a legal document with the approval number issued by the State Pharmaceutical Product Supervision and Administration to pharmaceutical production enterprises. Generally speaking, it is the "birth certificate" of this drug, which is also commonly known as the "production approval number". For the same drug, if the policy allows, many pharmaceutical companies may apply for registration. After passing the national examination, many pharmaceutical companies will approve the production, so each pharmaceutical company will have the drug registration approval number of the drug, but the approval number is different. The "new drug certificate" refers to the institution issued by the State Pharmaceutical Products Supervision and Administration to the qualified new drug applicants through a comprehensive review of the application materials for new drug registration (refers to the institution that submits an application for drug registration, bears corresponding legal responsibilities, and holds a drug approval certificate after the application is approved. ) legal ownership documents, but also the new drug "drug registration approval". Only one enterprise in China holds a new drug certificate and can produce the drug within the time specified in the Measures for the Administration of Drug Registration. "New drug certificate, production approval" and other forms of approval have never been seen. According to the regulations, the "new drug certificate" is transferable, but the "production approval" is not transferable.
Question 9: How to handle the approval of API production? This program is very troublesome. First of all, you have to study the synthesis and inspection of raw materials. After detailed research, you will form application materials and report them to the State Administration of Medical Supplies. The evaluation center of the State Administration of Pharmaceutical Products will send you a production approval after considering that your research meets the requirements and the raw materials produced are safe, effective and stable. Conditional nails must be declared by the manufacturer holding GMP certification certificate. There are many related situations. You can check the relevant provisions in the Drug Administration Law or contact me. I am now engaged in drug research and development. [E-mail protected]