The Knowledge


Preparation of the pharmaceutical registraton applications requires working knwoledge of local laws and regulations.


With successful track record of preparation and filing pharmaceutical registration packages, Novoclinica will deliver on timely registration of your next product in Russia.



 Would you like to get expert guidance in the pharmaceutical registration process?

Novoclinica offers pharmaceutical registration services that enable our partners to gain timely market approval for new pharmaceutical products in Russia. By focusing on diligent preparation of the documentation package in compliance with local laws and regulations, planning and follow up with regulatory authorities we ensure efficient review and approval process.   

Our pharmaceutical registration services include:
  • Pharmaceutical registration planning
  • Preparation of the pharmaceutial registration package 
  • Filing the package with local regulatory authorities
  • Tracking review and approval process
  • Obtaining the registration certificate
Lean more about our clinical trial regulatory affair services »

Our vision 
for better medicine helps us communicate the value of bringing new pharmaceutical products to market. 

We believe that our passion for better medicine enables us to build efficient processes for gaining  regulatory approvals.

Regulatory Affairs
Would you like expert guidance in the clinical trial application process? 

Bioequivalence Services
Would you like to get approval for your generic product faster?  

Support Services
Are you looking for complete clinical trial solution?