Where can I know the information of the original drug?

The original research drug generally refers to the original patented new drug, which requires preclinical research (target screening-target confirmation-compound development-active compound screening-pharmacological efficacy evaluation-process development-preparation development), application for clinical and clinical research (clinical phase I-clinical phase II-clinical phase III), application for production approval, production and sales, where thousands of compounds need to be screened and strictly controlled. Most new drugs in China are innovative drugs, and there are very few real original researches. At present, only large multinational pharmaceutical companies have the ability to develop.

The drug information of the original drug can be found in various national pharmaceutical product administrations.

For example, FDA inquires about the information of original drugs, EMA European Drug Administration, French American Food and Drug Administration, German Federal Institute of Vaccine and Biomedicine (PEI), Italian American Food and Drug Administration and so on. In these official food and drug administrations, you can find the information of original drugs in various countries. It is troublesome to inquire about the original drugs in various national pharmaceutical product administrations, and it is more troublesome to integrate them. Need to query multiple websites, the efficiency is not guaranteed, except the information of original drugs in various countries.

Inquire about the original drug information of each country in the database.

It is convenient, fast and efficient to query the information of the original drug in the database. You can query the data of the original drug through the listed drug database.

Drugs approved by FDA in the United States can be screened by keywords according to drug name, active ingredients, reporting enterprise, application number, dosage form and route of administration, and then the information of the original drug can be inquired by selecting "New Drug Application" in the application type of conditional screening.

Original drug information

There is also a centralized drug database approved by the European Union, where you can query the detailed information, public abstracts, instructions and other related documents of the original drugs and 1000+ drugs listed in the European Union through centralized procedures. Drug approval number, specification, dosage form, route of administration, packaging and other information. Extracting PDF files from authorized product information helps users to obtain basic information of drugs conveniently. Users can query the date of drug approval, market conditions, indications, public abstracts, instructions, approval history documents and so on through the drug name, active ingredients, ATC code and company.

Original drug information

Of course, the original drugs of all countries can be queried in the global drug database, which contains nearly 2 million drugs from more than 40 countries around the world, and the original drugs and generic drugs can be queried.

Information of original drugs in various countries

The above is the inquiry method of the original drug, and it may be troublesome to inquire in the major food and drug administrations. It is more convenient to query the original drugs by using the database, which can effectively improve the query efficiency of the original drugs and facilitate the query. You don't need to open multiple websites at the same time, and you don't have to worry about translation. Support one-stop search for easy query. In addition to the drugs that have been listed, we can also learn about the data of new drug research and development, drug evaluation, drug sales, drug quality and so on.