Our Services
We take care of your success
Negotiating contracts with Investigators
Managing the contract (amendments, appendixes)
Preparing and collecting up to date documents
Acting on behalf of the Sponsor
Organizing the venues
Inviting Investigators, Study Coordinators, CRAs and Vendors
Preparing training schedules
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Preparing the route map for selected sites
Planning study milestones
Working on SOPs
Training site staff
Collecting all necessary documents
Selecting Vendors
Evaluating the services
Negotiating the collaboration agreements
Representing the Sponsor in every day contacts with Vendors
Our monitors conduct all types of visits onsite and remotely:
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Site evaluation visits
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Site initiations visits
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Interim monitoring visits
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Closeout visits
Designing CRF
Working on a paper and electronic version of CRF
Preparing tailor made eCRF
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Evaluating and selecting sites
Assessing Investigators
Assessing the capacity to conduct clinical trials
Investigating enrollment and retention rate in similar studies
Clinical Trials Audits
Pharmacy audits
Inspection Readiness Visits
Assisting while MHRA Inspections
Being up to date with regulatory requirements
Preparing documents
Submitting country specific documents to EC