Beijing JHYB Pharmaceutical Technology Co., Ltd
Declare& Manufacture Data

We own an R&D team consists of searches professional literature, rganic synthesize and develop new product, which can offer you all data and samples of Declare& manufacture API.

    Charge Standard:

Sort Illuminate Price (10,000)
I
have not came into the market in China or foreign countries:  
1）Manufacturing API and its pharmaceutics by synthesizing or 　semisynthesis; ≥200
2）Extracting from nature substance or extract active monomer 　and its pharmaceutics by fermentation; ≥180
3）Optical isomer and its pharmaceutics of known medicament 　making by splitting and synthesize. ≥180
4）Making multicomponent medicament has been come into the 　market into small component medicament. ≥160
5）New compound pharmaceutics. ≥150
II
 Change the manufacturing ways of the pharmaceutics have not come into the market in China or has been come into the market in foreign countries. ≥120
III
has been come into the market in foreign countries and has not came into the market in China.  
1）API and its pharmaceutics ≥100
2）Compound pharmaceutics ≥100
3）Pharmaceutics has changed the manufacturing ways ≥100
IV
 Change acid radical and base (or tantalum) of saline medicament has been come into the market, but don’t change the API and pharmaceutics of its pharmacological action. ≥80
V
 Change the dosage form of the medicament that has been come into the market in China, but do not change the manufacturing ways. ≥30
VI
 API and pharmaceutics that have the China Physic Standard. ≥20
     
     

Items are included in the hereinbefore:
1、Medicament name.
2、Evincive document.
3、Purpose and gist of setting up topic.
4、Summarize and opinion of the main researching result.
5、Medicament illuminate sample draft, draft out illuminate and the newest referenced 　literature.
6、Design sample of packing and label.
7、Summarize of data of pharmic research.
8、Research data and illuminate of the research of API manufacture technics; research 　data of recipe and technics of the pharmaceutics and illuminate.
9、Corroboration chemistry structure experimentation data and illuminate of the 　component.
10、Experimentation data and illuminate of the quality research.
11、Medicament standard draft and draft illustration, and provide the standard 　product and contrast product.
12、Inspection proces-verbal of the sample.
13、Origin and quality standard of the assistant material.
14、Examination data and literature of the stability research of the medicament.
15、Wrapper of the direct touch medicament and the select thereunder and the quality 　standard of the container.

Notice: It should pay other fee, if you need the data of pharmacological and toxicological the research and the data of the clinic research.

　　Reference: State Drug Administration <<Drug Registration and Administration >>2002

    There are two ways to get our service.
    A: Call us: +86-010-88593845, the professional will service for you.
 
    B: Please fill in the below form, we will contact you and provide you the solvent in three working 　　　　　days according to you information.
  Product name：
  Chemistry name：
  CAS NO：
  Molecular formula：
  Structure：
  New drug sort
Sort Illuminate choose
I
have not came into the market in China or foreign countries:  
1）Manufacturing API and its pharmaceutics by synthesizing or 　semisynthesis;
2）Extracting from nature substance or extract active monomer 　and its pharmaceutics by fermentation;
3）Optical isomer and its pharmaceutics of known medicament 　making by splitting and synthesize.
4）Making multicomponent medicament has been come into the 　market into small component medicament.
5）New compound pharmaceutics.
II
 Change the manufacturing ways of the pharmaceutics have not come into the market in China or has been come into the market in foreign countries.
III
has been come into the market in foreign countries and has not came into the market in China.  
1）API and its pharmaceutics
2）Compound pharmaceutics
3）Pharmaceutics has changed the manufacturing ways
IV
 Change acid radical and base (or tantalum) of saline medicament has been come into the market, but don’t change the API and pharmaceutics of its pharmacological action.
V
 Change the dosage form of the medicament that has been come into the market in China, but do not change the manufacturing ways.
VI
 API and pharmaceutics that have the China Physic Standard.
  Existent and knew synthesize course：
  Scheming manufacture scale：
  Scheming date of coming into the market：
  Introduce of manufacture equipment in existence：
  Intending cost of manufacture the medicament：
  Prospective sell price of the medicament：
  Requirement：
  Declare& manufacture fee：
  Your company name：
  If have GMP YES NO
   
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Beijing JHYB Pharmaceutical Technology Co., Ltd 2007
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