How to apply for a TCM name

1) If the application materials are complete and meet the statutory form requirements, the accepting agency shall accept it and issue an administrative license stamped with the State Food and Drug Administration to the registration applicant.

A special seal for acceptance and a dated "Notice of Acceptance".

2) The acceptance numbers of the application for the reissuance of domestic health food new products, renewal of registration, change of registration, transfer of technology, and certificate reissuance are: Guoshijianshen G+4-digit era number + 4-digit sequence number, Guoshijian Continuation G+4-digit era number + 4-digit sequence number, Guoshijian G+4-digit era number + 4-digit sequence number, Guoshijian transfer g+4-digit era number + 4-digit sequence number, Guoshijian supplement G+4-digit era number + 4-digit sequence number.

3) The acceptance numbers of the application for the re-issuance of new products of imported health food, renewal of registration, change of registration, transfer of technology, and certificate reissuance are: National Food Jian Shen J + 4 digit era number + 4 digit sequence number, National Food Jian Continuation Library J + 4 digit era number + 4 digit sequence number, National Food Jian Jian J + 4 digit era number + 4 digit sequence number, National Food Jian Supplement J + 4 digit era number + 4 digit sequence number.

1) After accepting the application materials, the receiving institution shall send the application materials to the Health Food Evaluation Center of the State Food and Drug Administration (hereinafter referred to as the Evaluation Center) within 3 working days.

2) The Evaluation Center shall verify and fill in the "Transfer Form of Application Materials for Health Food Registration" on the day of handover, and sign for the receipt of the application materials.

Functional expert review responsibilities of the health function review team.

2) Review the suitable population, unsuitable population, edible method and consumption amount of the sample draft of the label instructions;

3) If non-stereotyped samples are used in the animal test of health function, and different batches of samples are used in the population consumption evaluation test and the animal test and safety evaluation test of health function, suggestions are made for the on-site verification of the trial production of the sample.

Hello, how to apply for the quasi-brand number of traditional Chinese medicine formula: the application process of the quasi-brand number of the drug is still complicated, generally: sample trial production - sampling by the provincial food and drug supervision and administration department of the manufacturer - qualified filing inspection - registration application to the provincial food and drug administration of the manufacturer - preliminary review by the provincial bureau - acceptance - on-site verification and sampling - re-inspection - data submission for review - data correction - approval.

Of course, if you want to apply for a company that you don't know or want to apply as soon as possible, you can find a professional agency to apply. "National medicine quasi-word" is the drug production approval number obtained by the drug production unit before the production of new drugs, after strict approval by the State Food and Drug Administration, which is equivalent to a person's ID card. Its format is:

The quasi-word of Chinese medicine + 1 letter + 8 digits of the number is chaotic filial piety, of which the letter used in chemical medicine is "h", the letter used in traditional Chinese medicine is "z" and so on. The condition for applying for the national drug approval word is that the drug can pass the review of the Food and Drug Administration to obtain the "Good Manufacturing Practice" certification certificate, and the "Drug Production License" can be obtained before it can be produced, and the "Drug Business License" can be sold only if it is Shenque is required.

Summary. The process of applying for the quasi-brand number of traditional Chinese medicine formula: 1. Application form for product registration of the State Food and Drug Administration.

2. The production site audit opinions issued by the provincial health supervision department shall be submitted in the following order. 1. Production site audit form 2, application form for health related product manufacturer health condition audit 3, product formula, product instruction manual, label 4, production process brief description and diagram 5, production equipment list 6, manufacturer health license, GMP certification certificate 7, other information.

Hello dear Chinese medicine formulas need to prepare the product registration application form of the State Food and Drug Administration in order to apply for the quasi-trade number.

The process of applying for the quasi-brand number of the traditional Chinese medicine formula group tour: 1. The application form for product registration of the State Food and Drug Administration. 2. The production site audit opinions issued by the provincial health supervision department shall be submitted in the following order.

1. Production site audit form 2, application form for health related product production enterprises to audit health conditions 3, product formula, product instruction manual, label 4, production process description and diagram 5, production equipment list 6, production enterprise celery industry health license, GMP certification certificate 7, other information.

3. The inspection report and related information issued by the product identified by the inspection agency shall be submitted to the examination and approval department in the following order: 1. Inspection application form 2. Inspection acceptance notice 3. Product manual 4. Sampling list 5. Physical and chemical inspection report 6. Safety inspection report 7. Other inspection reports.

Fourth, the process of administrative licensing of the National Drug Pants Supervision Bureau. Approved to obtain the relevant procedures of the State Food and Drug Administration and the health department: 1. Product implementation standard number 2, product standard audit form 3, national authoritative test report 4, product packaging design 5, product packaging record 6, authorization agreement 7, SC quality certification 8, production enterprise health license slag certificate 9, and other relevant information.

5. The following basic materials need to be submitted for product approval: 1. Product description, process flow filial piety rough process, 600 grams of test samples 2, business license, organization certificate, tax registration certificate 3, legal person ID card, patent certificate, trademark certificate 4, production license, GMP factory certification certificate Qiaofeng Town 5, foundation digging to provide entrustment certificate.

Hello, how to apply for the quasi-brand number of traditional Chinese medicine formula The application process for the quasi-brand number of the drug is still complicated, generally: sample trial production - sampling of the provincial food and drug supervision department of the production enterprise - qualified for filing and inspection - application for registration to the provincial food and drug administration of the manufacturer - preliminary review of the provincial bureau - acceptance - on-site verification and sampling - re-inspection - data submission for review - data correction - approval. Of course, if the company wants to apply for it if it does not particularly understand or wants to apply as soon as possible, it can find a professional agency to apply.

"National drug quasi-word" is the drug production approval number obtained by the drug production unit after strict approval by the State Food and Drug Administration before the production of new drugs, which is equivalent to a person's ID card. Its format is: Chinese medicine standard word + 1 letter + 8 digits, of which the letter used in chemicals is "H", the letter used in traditional Chinese medicine is "Z" front socks and so on.

The condition for applying for the national drug approval word is that the drug can pass the review of the Food and Drug Administration to obtain the "Good Manufacturing Practice for Drugs" certification certificate, and the "Drug Production License" can be produced only if it is obtained, and the "Drug Business License" can be sold only after it can be obtained.

What are the Chinese patent medicines at the beginning of the name Jianzi: Jianji Soup, Jianlan Leaf Paste, Jianling Soup, Jianling Cream, Jianspleen Li Zhong Tang, Jianspleen Ginseng Pill, Jianspleen San, Jianspleen Soup, Jianspleen Pill, Jianjia Dan, Jianjia Powder, Jiangao Pill, Jianyuan Dingchuan Soup, Jianzhong Dan, Jianzhong Huangqi Soup, Jianzhong Jiaaconite Angelica Soup, Jianzhong Jiaminus Soup, Jianzhong Jiapapaya Bupleurum Soup, Jianzhong San, Jianzhong Soup, Jianzhong Tori Soup, Jianzhong Pill, etc.