Clinical Trial Site Activation Support
From submission to approval. Driving site readiness for clinical trial participation.
We streamline site-level clinical trial start-up by managing clinical trial agreements, budget negotiations, regulatory submissions, ethics approvals, and institutional documentation.
Our team ensures sites are compliant, prepared, and ready to initiate trials efficiently, helping investigators and sponsors reduce start-up timelines while maintaining the highest standards of quality and research integrity.
Areas of Focus
Budget negotiations
We will support your budget negotiations with the Sponsor.
Clinical trial agreement liaison
We will work with the Contracts Office to facilitate and execute the clinical trial agreement.
Ethics and impact submissions
We will prepare and submit the trial for ethics and impact approvals.
Site-level regulatory documents
We will navigate the collection, review, and submission of the required site essential documents.
Training and readiness
We will coordinate the delegation and training requirements and confirm your site’s readiness for site initiation.