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New Hires

 Our Services

We take care of your success

Contracts management


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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Site set up


Preparing the route map for selected sites

Planning study milestones

Working on SOPs

Training site staff

Collecting all necessary documents

Vendors management


Selecting Vendors

Evaluating the services

Negotiating the collaboration agreements

Representing the Sponsor in every day contacts with Vendors

Clinical monitoring


Our monitors conduct all types of visits onsite and remotely:

  • Site evaluation visits

  • Site initiations visits

  • Interim monitoring visits

  • Closeout visits


CRF design

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

Audits and QA/QC services


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

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