Conducting a robust feasibility study is a pre-requisite to initiating a clinical trial. Accurate data is of key importance when making a decision on whether to conduct a clinical trial in a particular country. RemediumOne consists of a dedicated start-up and regulatory team who are well experienced in carrying out topline and detailed feasibility assessments efficiently. RemediumOne works with investigators of international caliber, trained in various global centers of repute. The investigators from our investigator database are selected based on their experience in the respective therapeutic areas and professional reputation and standing.


Regulatory affairs


Safety reporting

Admin and logistics

Site space management

Project management

Quality management

Recruitment and retention


400+ Topline feasibility


100+ Detailed feasibility


3-4 working days average turnaround time