Drugs & Cosmetic Act 1940 & Rules
The preindependance durgs and cosmetic act was amended in the year 1955 after Indian gained independance. Subsequently the act was amended a number of times as late as 2008. The acts come under the purview of Ministry of Health & Family Welfare.

The advisory body are :

The Drugs & Advisory Board
The Central Drugs Laboratory
The Drugs Consultative Comittee

The participation is at various level usually between the State and the Central Government. The Government depends upon these representative bodies for technical advise and recommendations.

In India Drugs and Cosmetics Act 1940 and Drugs and Cosmetic Rules 1945 regulates manufacture, import and distribution of bulk drug (API) and finished formulations. The drugs and the manufacturing facility have be registered before import. The New Drug (Rule 122 E of the Act) approval is pre-requisite for submission of application for Registration and or
import. This can be done by the Local Authorized Agent on behalf of the foreign manufacturer.


We also provide services for
  • Blood Bank and Blood Product Registration
  • NOC for Import of Half finished or Raw materials
  • Loan Licensing
  • Legalization of Export/Import documents
  • Neutral Code Licensing