The Expertise

The success of generic pharmaceutical program is often based on timely recruitment and robust protocol design for the bioequivalence study. 

With its expertise in clinical development process, Novoclinica will help your next generic product get to market faster.

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

Novoclinica provides a range of services for generics. We focus on bioequivalence studies to ensure rapid study start-up and execution in accordance with GCP guidelines.
 
Our bioequivalence services include:
  • Ensuring regulatory and ethics committee approval, learn more » 
  • Validation of assays for measuring the drug and its metabolites in biological samples
  • Timely subject recruitment
  • Executing the study protocol
  • Pharmakinetic and statistical data evaluation
  • Reporting of study results
  • Closing out the study and ensuring records transfer
« back to Clinical Operations

Our vision for better medicine puts clinical operations at the core of our business. We believe that by focusing on clinical operations we deliver exceptional value to our partners. 

We see Novoclinica as an extension of our partner's team working together towards a common goal of bringing better medicine to the patients.



Clinical Operations
Would you like to assure quality and consistency of your clinical data? 

Pharmaceutical Registration
Would you like to register your new product in Russia? 

Laboratory Services
Does your clinical trial protocol call for laboratory testing?