Clinical Trial Delivery
Our core business is to deliver on complex clinical trials in partnership with our Sponsors and Contract Research Organisations (CRO) at our dedicated research site.
We work to provide accurate, reliable and consistent research data, while ensuring the safety and well-being of trial participants, across three areas of activity:Β Β
Study Feasibility and Setup
Feasibility information supplied within 48 hours of request
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Protocol assessment and trial design capacity
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Ethics and regulatory submissions packages
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Timely budgeting and contracting
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Comprehensive and accurate enrollment forecasts
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Experienced team to expedite study set-up
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Identification and set-up of local vendors
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Expertise in providing rescue site services
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Protocol assessment and trial design capacity
π
Ethics and regulatory submissions packages
π
Timely budgeting and contracting
π
Comprehensive and accurate enrollment forecasts
π
Experienced team to expedite study set-up
π
Identification and set-up of local vendors
π
Expertise in providing rescue site services
Clinical Trial Management
Each trial is managed by a dedicated project team
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Through robust governance our leadership team has oversight of all clinical operations
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National Chief Investigator (NCI) and Chief Investigator (CI) capabilities
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Experienced GMC licensed Principal and Sub-Investigators
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In-house quality assurance team works to ensure that trial data and processes are audit ready
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Close connection to participants' primary care and specialists
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Our Quality Management System has been built on accreditation for ISO 9001:2015 gained over eight years
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Through robust governance our leadership team has oversight of all clinical operations
π
National Chief Investigator (NCI) and Chief Investigator (CI) capabilities
π
Experienced GMC licensed Principal and Sub-Investigators
π
In-house quality assurance team works to ensure that trial data and processes are audit ready
π
Close connection to participants' primary care and specialists
π
Our Quality Management System has been built on accreditation for ISO 9001:2015 gained over eight years
Participant Engagement
Access to diverse populations and patients with rare and difficult to treat diseases
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In house specialist recruitment team devise targeted strategies using a mix of traditional and innovative approaches
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Advertising and participant facing materials for ethics submissions
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Patient and Public Involvement (PPI) projects for ethics submissions
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In house database holds over 24,000 individuals across a range of therapeutic areas and a broad demographic spectrum
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Thorough pre-screening process to ensure eligibility which allows us to maintain a high screening to randomisation ratio
π
In house specialist recruitment team devise targeted strategies using a mix of traditional and innovative approaches
π
Advertising and participant facing materials for ethics submissions
π
Patient and Public Involvement (PPI) projects for ethics submissions
π
In house database holds over 24,000 individuals across a range of therapeutic areas and a broad demographic spectrum
π
Thorough pre-screening process to ensure eligibility which allows us to maintain a high screening to randomisation ratio
General consultancy services
Through our world leading clinical and scientific specialists we offer strategic and practical advice to sponsors on their drug development programmes, especially in the fields of pain and cognition.
This includes Proof Of Concept study design and execution, as well as Protocol Development.Β