Project Management and Clinical Trial Conduct
Project management and phase trials conducted in line with ICH GCP and local regulations.
DetailsOur Services
We support you at every stage, from planning through to reporting of the clinical trial.
Ethics Committee and Ministry of Health Applications
Ethics committee submission, approval and Ministry of Health authorisation at the capacity and speed sponsors expect.
DetailsStudy Coordinator
Study coordinator services delivered by ICH GCP-trained staff, matched to the trial design.
DetailsContract Personnel
Sourcing and employment of contract personnel according to company requirements.
DetailsClinical Trial Document Provision
Provision of trial documents in line with ICH GCP and local regulations.
DetailsData Entry / Management
Case report form design, electronic data capture software and data entry services.
DetailsPharmacy and Medical Device/Supply Provision
Provision and logistics of medicines, consumables and medical devices required for clinical trials.
DetailsClinical Trial Supply Management
End-to-end supply and logistics management of devices, consumables and equipment — including calibration, storage and return processes.
DetailsCustoms Services
Management of import, export and customs clearance processes for investigational products and biological samples.
DetailsConsultancy Agreement Preparation and Follow-up
Preparation, execution and follow-up of contracts between sponsors, investigators and institutions.
DetailsEarly Access Programme Applications and Management
TİTCK submissions and programme management for delivering unlicensed medicines to patients.
Details