Clinical Research Delivery for Sponsors & CROs
Orizzonte delivers healthcare-integrated clinical research through Research-Enabled Visit Centres, with every study assessed for feasibility and fit.
Research delivery connected to healthcare
Orizzonte’s model enables appropriate clinical research to be delivered through Research-Enabled Visit Centres established within partner GP practices.
These Visit Centres provide dedicated local research capability within the primary-care environment, while Central Research Operations support coordination, operational planning and oversight across the network.
The delivery model is determined by the requirements of each study. Some studies may be suitable for Visit Centre delivery, while others may require specialist, hospital or combined pathways.
Explore Orizzonte’s Capabilities
Research Delivery
Therapeutic Areas & Capabilities
Visit Centres
Coordinated Research Infrastructure
Orizzonte brings together local research delivery and central operational oversight to support consistent study delivery across the network.
Research-Enabled Visit Centres
Dedicated research capability established within partner GP practices.
Central Research Operations
Central coordination supporting planning, start-up, Sponsor and CRO communication, operational delivery and oversight.
Protocol-Led Feasibility
Study opportunities assessed against protocol requirements, participant populations, available capability and operational feasibility.
Quality & Governance
Governance and quality systems supporting participant safety, regulatory compliance, data integrity and consistent research delivery.
Research-Enabled Visit Centre Network
Orizzonte’s current network includes Research-Enabled Visit Centres across London and Hertfordshire.
Have a Study to Discuss?
If you are considering Orizzonte for a clinical study, contact our team to begin an initial discussion about the study and its delivery requirements.
For an initial enquiry, useful high-level information may include:
- therapeutic area or indication;
- target participant population;
- anticipated UK timelines; and
- broad delivery or location requirements.
Detailed or confidential study information can be shared through an appropriate route once contact has been established.
Frequently Asked Questions
Every study opportunity is considered individually according to protocol requirements, participant safety, clinical capability and operational feasibility.
No. Some studies require specialist or hospital-based infrastructure, while others may be suitable for Visit Centre or combined delivery.
The appropriate model is determined through feasibility.
Where a study is suitable and the required capability is available, Orizzonte’s centrally coordinated model is designed to support delivery across multiple Visit Centres.
Orizzonte can be engaged during feasibility when sufficient study information is available to consider protocol requirements, participant populations, infrastructure capability and operational feasibility.
Discuss Your Study
Talk to Orizzonte about protocol requirements, feasibility and healthcare-integrated clinical research delivery through our Research-Enabled Visit Centre network.