Clinical Research Organization in Lithuania

cro europe

Clinical trials in Latvia can be conducted by OCT, the leading CRO in Latvia.

Full service clinical research in Lithuania is better to be committed to OCT. Its’ qualified personnel counts 150 people. The company has completed over 200 clinical trials. OCT’s Pharmacovigilance team covers a range of clinical trial safety monitoring and safety reporting tasks and responsibilities for our clients’ studies.

OCT Pharmacovigilance services include:

  • Set up of PVG specific processes and procedures
  • Evaluation of safety data
  • Case receipt
  • Data entry
  • Adverse eventq triage
  • MedDRA coding
  • Narrative writing
  • Medical review
  • Quality control
  • CRF review
  • Reporting of SUSARs to regulatory authorities in all countries of OCT operation
  • Reporting of SUSARs to study sites
  • Preparation and submission of periodic reports to regulatory authorities in all countries of OCT operation
  • Preparation and submission of Annual Safety Report to study sites.

As a result, we bring together our PVG process expertise and the regulatory insights to deliver safety reports of high quality on time and in compliance with the sponsor’s budget.

Our office in the Baltic States

Riga

Udens iela 12, suite 52, Riga, LV-1007, Latvia
 +371 (676) 954 86  +371 (676) 954 87  
 baltic@oct-clinicaltrials.com

Meet us at upcoming events


loading map...