Registration

«Grindeks» has a wide sales network and great experience in the market as well as all resources necessary to provide contract registration services to meet the clients demands:

1) Packaging development in compliance with the specific legislation of a particular country - we can produce the entire packaging set from the information on the packaging to readability testing of product information leaflet in the Europe and the CIS.

2) Readability testing of product information leaflets

3) Translation of the Drug Registration Documents and adaptation to the particular country market

4) Entire development of drug registration documents in CTD, eCTD in compliance with the EU requirements as well as development of drug registration documents in compliance with the CIS countries requirements

5) Drug registration process steering and co-ordination.