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PRUDENTAS is a contract research organization registered in March 2007 and headquartered in Moscow, Russia. The company appeared in response to the growing interest of pharmaceutical and biotech companies in conducting clinical trials in Russia and Ukraine.

PRUDENTAS employs a committed team with sufficient experience and expertise to conduct proof-of-concept studies.

PRUDENTAS offers the following services for Phase I – IV trials in Russia and Ukraine:

  • Study documents preparation
  • Study Start-Up
  • Regulatory support of the study
  • Project Management
  • Clinical trial monitoring
  • GCP training for investigators
  • Safety Monitoring
  • Site Management
  • Clinical Trial Logistics
  • GCP Auditing, preparation for regulatory inspection, audits support
  • Management (Subcontracting) of Russian Central Lab, Warehouse
  • Subcontracting Data management and Biostatistics providers

PRUDENTAS has a large experience in preparation / translation / adaptation of clinical trial documents fulfilling the GCP guidelines.

PRUDENTAS specialists have extensive experience in conducting Phases I-IV clinical trials for different groups of patients (adults, children) in various therapeutic areas:

  • Blood disorders
  • Neurology
  • Oncology
  • Cardiology
  • Psychiatry
  • Pulmonology
  • Gastroenterology
  • Rheumatology
  • Dermatology
  • Autoimmune Disorders
  • Nephrology
  • Urology
  • Infection diseases
  • Endocrinology
  • Ophtalmology

Contact details:
Address: 12, Building 1, Krivokolennyi per., Moscow, 101000, Russia
Phone: +7 (495) 6283802
Fax: +7 (495) 6283633
E-mail: contact@prudentas.com
Website: http://www.prudentas.com/

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