How We Work
Our project management team works with you from the outset, so that every component of your study is properly planned for and carried out.
- 1
Enquiry and proposal
Tell us about your study. We review its requirements and send a proposal with timelines and costs.
- 2
Planning and approvals
We write the clinical study protocol and supporting documents, and prepare the study for regulatory and ethics approval.
- 3
Clinical conduct
Volunteers are screened, enrolled and cared for in our 30-bed clinical unit, under GCP and our SOPs.
- 4
Bioanalysis
Samples are analysed on LC-MS/MS in our own laboratory, using methods validated to global regulatory requirements.
- 5
Reporting
We prepare the clinical study report as per the related regulatory requirements.
Along with cooperating with the sponsor, the team promotes proactive and timely communication through regular teleconferences, and our independent QA team audits every stage.