Services

Provision of Contract CRAs in the UK and Europe

All CRAs are experienced to ICH-GCP and can perform:

Study management
Monitoring plan, timing and logistics
Monitors internal pre-study meeting
Investigator pre-study visit
Co-ordination of investigators' meeting
Study initiation site visit
Regular monitoring visits / telephone contacts
Adverse event reporting
CRF monitoring, collection, transport
Source data validation
Drug accountability check
Correction/query resolutions
Visits for study closure

Study Management

Klinikos can ease the burden on your medical dept. by providing management of the field based CRAs on your study. In this way, your company can focus on the whole trial yet maintain overall control of the project.

Investigator Site Research Nurses

To assist Investigator sites Klinikos has a bank of experienced study site co-ordinators in the UK. All are fully ICH-GCP qualified having worked on a range of clinical trials and all hold UKCC registrations.

Investigator Sites

Patient delivery is key to a successful trial. Klinikos has a database of pre-qualified Investigators in various therapy areas (GPs and hospitals throughout the UK) for Phase II -IV clinical trials.

ICH-GCP training of Investigator site personnel

Always a crucial issue to the smooth running of a trial, the increase in Phase IV studies and subsequent number of investigator sites, demands a greater need for site personnel training.

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