Investigator Meeting Organization:


Klinar CRO organizes investigator meetings at the start of the study, during the study and/or at the end of the study. These meetings are conducted in order to provide study specific information to investigators, to increase patient recruitment, to evaluate the current state of the study and/or to inform investigators about the progress of study. Meeting agenda is prepared in cooperation with sponsor and meeting binders can be prepared by Klinar CRO if requested.


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.


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.


Training Organization:

  • Planning of training program according to needs of pharmaceutical companies
  • Design of training material
  • Organization and application of training program
  • Organization of ICH-GCP and/or project specific investigator trainings