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