If your university team or Clinical Trials Unit (CTU) is at full capacity and you’re struggling to get your trial off the ground, we’re here to help. Our team has extensive experience working with NHS and University teams in phase I, phase II, phase III and Phase IV trials (IMP and Medical Devices) across a broad range of therapeutic areas.
Expedite your clinical trial using our specialist CRO team
We’re your partner, not just a CRO
We understand there is a lot to navigate when you’re approaching the clinical trial stage of your research journey. We’re here to help from the early stage, even before your funding has come through and at no extra cost. We can work alongside your Translational Research Office (TRO), if applicable, to provide guidance on grant applications, protocol development and resource requirements in order to achieve the best outcome for your trial. Our flexible service model means we can dovetail our services with your available resources making it an efficient and effective partnership.
Benefit from flexible ‘pick and mix’ services
- Free Advice & Guidance Pre-Funding
- Protocol Development
- UK Regulatory Approvals
- Site Set Up and Initiation
- GCP/ISO Trained CRA Monitoring
- EDC/Data Management
- Safety Management & Reporting
- Statistics & Data Management
- ISO Accredited Quality Management System
Shared success through collaboration and transparency
At PHARMExcel, we foster strong, collaborative relationships with our sponsors and sites ensuring proactive communication and a firm commitment to understanding your needs. As we are a smaller UK CRO, the team introduced during initial interactions remains consistent and accessible throughout your project, fostering stability and accountability for the trial.
"I have worked with Yvanne Enever and the PHARMExcel team for several years on a complex, multicentre Phase 1 vaccine study. I have found them be efficient, highly professional while being accommodating and very supportive. I have worked with other clinical trial research organisations on similar studies and PHARMExcel have been by far the most effective in achieving targets and the easiest to work with on a day to day basis. "
Dr Kim Orchard, Senior Lecturer and Consultant Haematologist, University Hospital Southampton NHSFT
"Yvanne and her team at PHARMExcel are the best team I’ve worked with in liver-related clinical trials. They are talented and committed individuals with great expertise in the regulatory landscape as well as delivery of clinical trials. Highly recommended!"
Dr Gautam Mehta, Hepatologist and Principal Investigator, University College London
"It has been a pleasure working with Yvanne and the team. PHARMExcel have been able to work with our clinical research teams to provide bespoke support for a number of trials, including phase 1 studies: the personal approach and attention to detail have given us confidence to ensure patient safety and manage the risks of the Trust acting as Sponsor in particular for the early phase trials."
Karen Underwood & Professor Saul Faust, Sponsor, University Hospital Southampton NHSFT
"PHARMExcel are very interactive and excellent in communicating with clinical teams. They have a thorough understanding of the regulatory requirements for managing GCP compliant clinical trials. I have no hesitation in recommending them as a CRO."
Dr Kim Orchard, Senior Lecturer and Consultant Haematologist University Hospital Southampton NHS FT
"PHARMExcel’s passion for their projects, the professionalism shown by the team, combined with direct access to the CEO sets PHARMExcel apart from other CROs."
Prof James Moore, Imperial College
"The support from PHARMExcel has been extremely high quality. This includes all aspects trial development, management and monitoring, that was also evidenced by a recent sponsor audit. We look forward to working with PHARMExcel going forwards."
Tom Fletcher, CST-6 Candidate Chief Investigator, Director Global Health Trials Unit,
Liverpool School of Tropical Medicine
Gain peace of mind from our quality & risk-based approach
- Patient-Centric Study Design
- Study Specific Risk & Safety Management Plans
- ISO Certified Quality Management System
- Rapid Development of Study-Specific Procedures
- Risk-Based Monitoring Methods
- Experienced CRAs
- Experienced Clinical Quality Auditors
We bring value-add to academic and IIS trials
Learn more about our successful CRO-Academic partnerships
