Clinical trials

Study feasibility
  • Availability of a target population of patients and research centers
  • Quantitative assessment of patient recruitment potential in centers and their location
  • Availability of the necessary facilities / equipment / lab tests / concomitant medications
  • Influence of ongoing or planned competing studies
  • Identification of other potential risks, challenges, and bottlenecks
Consultations on supply chain management of clinical trial materials
  • Consultation on obtaining an import license for an IP / Concomitant therapy and biological samples in the Ministry of Health of the Russian Federation
  • Consultations and selection of a vendor to ensure cold chain conditions for logistics and storage of biological samples
  • Cold chain temperature monitoring
  • Selection of vendors for the storage, shipment, and destruction of clinical trial materials according to the GxP
Consultations on the selection of vendors for organization clinical trials in Russia
  • Translation Agency
  • Warehouses and logistics
  • Central laboratory services
Organization services (Phase I – IV, bioequivalence)
  • Regulatory support
  • Project management
  • Clinical monitoring
  • Medical monitoring
  • Quality assurance and quality control

The Duopharm team will help you organize and conduct early-stage and bioequivalence clinical trials, as well as provide consulting support for late-stage clinical trials. By entrusting the Clinical Trials to DuoPharm professionals, you are guaranteed to get:

We will help you set up processes for organizing clinical trials in both large research centers and small institutions with complex logistics chains. In accordance to your request DuoPharm will evaluate the feasibility of conducting clinical trials in Russia before the start of the study. We’ll help you form a “third” opinion for making an informed and right decision in the beginning of your project.

Any questions left?

Call +7 812 967 88 87 or leave your enquiry in the form below

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