Our services
A complete approach
for inclusive clinical trials
Centrally managed sites with dual UK hubs, consistent
SOPs and extended access hours.
AI-driven patient identification, community outreach and dedicated retention teams.
Regulatory support, data monitoring, diversity plan writing, safety oversight and QA.
While we provide complete trial delivery, our model is designed first and foremost around optimising recruitment and ensuring first-class care for patients.
At Frontier, we cover this process
from start to finish.
Research Sites
Patient
Engagement &
Recruitment
Functional
Service
Provision
Privacy-Preserving AI
Research Sites
Run your trial through our centrally managed site network, optimised for accessibility, efficiency and global expansion.
This includes:
- Use of e-Technology (CTMS, eConsent, eCoA etc.)
- In-house monitoring and quality assurance
- Centralised management
- Project management
- Budget and CTA negotiations
- Invoicing and payments
- Monitoring and safety oversight.
Patient Engagement and Recruitment
Connect to patients faster with our unique, ongoing engagement in the community.
- Access to over five million live patient electronic medical records (EMR)
- Continuous community, disease association and advocacy group outreach by dedicated patient engagement team
- Provision of personalised patient support from screening to enrolment, boosting conversion and retention
- Growing database of trial volunteers
- AI-powered patient identification
- Focus groups and market research.
Functional Service Provision
Get expert support with a range of customised defined services at every stage of your trial.
- Regulatory and ethics submissions
- Medical monitoring
- Project management
- Medical writing
- Clinical trial monitoring
- Quality assurance
- Diversity plan writing.
Proprietary AI Model
Matching millions of patient electronic medical records to clinical trial protocol inclusion / exclusion criteria using state-of-the-art privacy preserving data pipelines.
- Rapid matching with the ability to identify patients from vast, highly varied data-sets
- Strong standards-based anonymisation
- Interoperable AI capable of being used across any PAS, EMR and other data-sources
- Built on principles laid out by the (UK / EU) GDPR and future AI regulations
- Continuous monitoring and testing for recall of sensitive information throughout development cycle
- No storage of queries, with strict consenting and re-consenting procedures in place.