PHARMExcel
PHARMExcel is an ISO accredited Contract Research Organisation (CRO) providing Phase I-IV clinical research services across various therapeutic areas including Hepatology, Oncology, Infectious Diseases, Ophthalmology, and more. They focus on delivering high-quality, collaborative, and flexible clinical trial solutions, supporting academia, biopharma, medical devices, and biotech companies. Their mission emphasizes tailored, innovative approaches, quality, transparency, and building long-term partnerships. They are committed to supporting charities and community initiatives, including Dementia UK, Isabel Hospice, Alzheimer’s Research UK, and local foodbanks.
Industries
Nr. of Employees
small (1-50)
PHARMExcel
Stevenage, Herefordshire, United Kingdom, Europe
Services
Development of study protocols, patient information and consent documents, and clinical study reports to regulatory and publication standards.
Preparation and management of clinical trial applications, amendments and notifications for competent authorities including device regulatory support for UK & EU frameworks.
End-to-end study and project coordination including planning, timeline management, vendor oversight, and real-time reporting to keep projects on track and on budget.
Hybrid monitoring strategies combining remote, central and on-site monitoring tailored by study risk to ensure data quality and protocol adherence.
Statistical planning and analysis including SAP development, randomisation schedules, interim analyses, DSMB outputs and TLF generation.
Provision and management of EDC platforms with real-time edit checks, role-based access, query management and integration with kit-tracking systems.
Development of study protocols, patient information and consent documents, and clinical study reports to regulatory and publication standards.
Preparation and management of clinical trial applications, amendments and notifications for competent authorities including device regulatory support for UK & EU frameworks.
End-to-end study and project coordination including planning, timeline management, vendor oversight, and real-time reporting to keep projects on track and on budget.
Hybrid monitoring strategies combining remote, central and on-site monitoring tailored by study risk to ensure data quality and protocol adherence.
Statistical planning and analysis including SAP development, randomisation schedules, interim analyses, DSMB outputs and TLF generation.
Provision and management of EDC platforms with real-time edit checks, role-based access, query management and integration with kit-tracking systems.
Expertise Areas
- Clinical trial management (Phase I–IV)
- Regulatory compliance and device approvals (UK/EU/MHRA)
- ATMP / cell and gene therapy trial operations
- Medical device clinical investigations (Class I–III)
Key Technologies
- Electronic Data Capture (EDC) - 21 CFR Part 11 compliant
- Electronic Trial Master File (eTMF)
- Risk-based monitoring (central/remote/on-site hybrid)
- Adaptive trial design methodologies
News & Updates
PHARMExcel was recognized for its excellence in clinical trial services.
The company participated in important discussions at the symposium.
A pioneering trial in oncology involving ATMP.
Recognition for innovation in medical device research.
An article exploring challenges and opportunities in liver disease trials.
A study on probiotics' effectiveness in SCI patients.
PHARMExcel was recognized for its excellence in clinical trial services.
The company participated in important discussions at the symposium.
A pioneering trial in oncology involving ATMP.
Recognition for innovation in medical device research.
An article exploring challenges and opportunities in liver disease trials.
A study on probiotics' effectiveness in SCI patients.