OCT Clinical Trials

Leading CRO in Eastern Europe

Eastern Europe is accepted by the pharmaceutical industry as an ideal region for conducting clinical trials due to its high enrollment rates, convenient access to patient populations, skilled investigators and centralized healthcare systems.

OCT provides the full-scale range of services to pharmaceutical, biotechnology and medical device companies. Our turn-key clinical trial solutions include Consulting and Regulatory Support, Medical Writing and Translation, Quality Assurance and Pharmacovigilance, Project Management and Clinical Monitoring, Data Management and Biostatistics, and Drug registration in Eastern Europe.

OCT’s strategy is to generate FDA and EMA-acceptable data by including most of the subjects in our studies in the EEU region while having small number of sites in the US and Europe. Such approach ensures the most optimal combination of fast reliable enrollment and low costs of studies by OCT.

Visit our website for more information www.oct-clinicaltrials.com

Contact Information

Olga Ivanova
Business Development Manager
OCT Clinical Trials
5 Kovenskiy per
Saint Petersburg 191014
Russia
(8812)4498634
OIvanova@oct-clinicaltrials.com
www.oct-clinicaltrials.com
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Experience

OCT is an experienced full-service CRO successfully operating in Eastern Europe. Our staff accounts for 150 professionals located in all countries of our presence. At the moment OCT has over 80 long-term partners with international pharmaceutical leaders and local manufacturers among them. With more than 200 projects performed to date, we have solid experience within different clinical phases and indications.

OCT’s strategy is to generate FDA and EMA-acceptable data by including most of the subjects in our studies in the EEU region while having small number of sites in the US and Europe. Such approach ensures the most optimal combination of fast reliable enrollment and low costs of studies by OCT.

Services

  • Consulting and Regulatory Support
  • Medical Writing and Translation of Study Essential Documents
  • Quality Assurance and Pharmacovigilance
  • Project Management and Clinical Monitoring
  • Data Management and Biostatistics
  • Drug registration
  • Why OCT

  • 12 years on the market
  • 8 offices in Russia, Europe and the US
  • Strong expertise in 21 therapeutic areas
  • 1600 investigational sites
  • 200+ clinical studies conducted
  • 150+ employees
  • 80+ long-term partners
  • 50+ system audits by big pharma companies with no major findings
  • Contact Information

    Olga Ivanova
    Business Development Manager
    OCT Clinical Trials
    5 Kovenskiy per
    Saint Petersburg 191014
    Russia
    (8812)4498634
    OIvanova@oct-clinicaltrials.com
    www.oct-clinicaltrials.com
    View Map

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