Optimum-cro – Optimum Contract Research Organization

Quality Management

OPTIMUM CRO has its self-check systems to provide improvement and control of quality in management of clinical studies. These systems consist of regular internal checks which are performed by separate QC unit

Study Protocol Design

In the protocol design procedure, overview of the study is discussed with sponsor and requested parameters are assessed. Trial protocol is finalized by a statistician and a medical advisor who is a specialist in the therapeutic area of the study. In this process, comments from sponsor and/or investigators are also taken into consideration

Laboratory Organization

OPTIMUM CRO takes part in organization of laboratories (both central and local) that will be included in the study to perform protocol-defined examinations.

OPTIMUM CRO was established in September 2000 as one of the first CROs in Turkey. Beginning from this date, many projects have been conducted, varying from international phase III and local phase II studies to post-marketing trials. More than 20 employees (including CRAs, PMs, QC and data management units) are located in the main office based in Ankara, the capital city of Turkey.

Feasibility Assessment for Site Selection

To decide on potential study sites by using detailed investigator database, Preperation of feasibility questionnaires based on study protocol,
Read More

Investigator Meeting Organization

OPTIMUM CRO organizes investigator meetings at the start of the study, during the study and/or at the end of the study.
Read More

CRF Design

This service includes design of study CRFs by project coordinators according to the study protocol and final review is performed by QC unit.
Read More

Quality Management

Study Protocol Design

Laboratory Organization

OPTİMUM is member of SAKDER