Consultation Services for Clinical Research Studies

We offer consultation services for sites participating in clinical research studies. Let us look after the paperwork so you can focus on what is important: your patients.

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We offer assistance with:

• Protocol and SOP development

• Feasibility assessments

• Informed Consent Form (ICF) creation

• Recruitment plans

• Ethics submissions through to REB approval

• Contract and budget negotiation

• Research team training

• Providing documents to the Sponsor

• Setup for source data collection tools

• Site Initiation Visit preparation

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