A track record you can trust with your trial.
In 14 years of operation, Obsidian has conducted over 100 clinical studies across 7 Western European countries, serving more than 50 sponsor companies in Europe and the US.
Ethics submissions handled with real fluency.
Gain peace of mind knowing Obsidian has extensive experience handling UK and Ireland ethics submissions for clinical trials — from NRES-compliant patient documentation to NIHR applications to the NHS Portfolio.
We understand the importance of feasibility studies in assessing site suitability, and we're on hand to present study materials at investigator and study-launch meetings.
Senior people, minimal overhead.
Feasibility studies
Thorough feasibility assessment to ensure successful clinical trial outcomes before you commit.
Investigator meetings
We assist at investigator meetings to streamline study launch and align every site from day one.
NHS Portfolio applications
All UK & Ireland ethics submissions and NIHR applications for your trial, managed end to end.
Routine site visits
Pre-study, initiation, interim monitoring and closeout visits, conducted with minimal management support.
Compliance assurance
Good site performance secured by reviewing informed-consent procedures and protocol compliance.
International reach
Studies delivered across Western Europe for sponsor companies in both Europe and the United States.
Breadth built over 100+ studies.
Vast therapeutic knowledge across the areas driving today's pipelines.
Interested in conducting successful clinical studies?
Put our experience to work on your next trial. Tell us what you're planning and we'll show you how we can help.
Contact us