Sponsor focused
Delivering more patients per site using a finely tuned site feasibility approach
Delivering more patients per site using a finely tuned site feasibility approach
Speed
- Enabling rapid site start-up with efficiencies gained by central process management including budgeting and contracting
Proof point: Typical timelines for EMEA – 2 weeks and US – 3 weeks
Sponsor Benefit
- Delivering more patients per site using a finely tuned site feasibility approach.
- A dedicated patient engagement team drive the identification and recruitment of suitable patients using EMR (in specific countries), an extensive database of pre-consented patients and targeted campaigns on digital channels.
- A healthcare partnership team connect with general practitioners to drive new patient referrals to our well established clinical research site network.
Proof point: XX patients per site in the last 6 months
Quality
- Ensuring quality and compliant services with the deployment of consistent processes, operating guidelines and tools across all sites.
- Proof point: 13 FDA Audits over 5 years with no findings, MHRA inspections in 2018 & 2019 with 1 major finding and no critical findings
