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:
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.