Clinical trials for Biotechs

Helping small to medium sized Biotechs optimise their clinical trials in the UK

Amplify your clinical trial capabilities with us

As your team and infrastructure scale up, and you strive to advance your novel therapy, you and your investors will be seeking increased assurance that your CRO partner will work collaboratively and effectively with you to expedite your clinical trial, laying the operational and clinical foundations for long term success in your commercial pathway.

Our experienced in-house team has experience across all key therapeutic areas and understands the different pressures faced by  growing companies including Start Ups and University Spin Outs. With our extensive UK networks, which include our Cancer Networks, Clinical Research Networks (CRFs) and our NHS sites, we can comprehensively deliver on all phases of research.​ We use existing intelligence gathered throughout our 15-year history to shape the success of your  trial delivery.

Our services & capabilities

  • Protocol Development
  • UK Regulatory Approvals
  • Site Set Up and Initiation
  • Monitoring & Site Management
  • Project Management
  • Safety Management & Reporting
  • Statistics & Data Management
  • ISO Accredited Quality Management System
  • ATMP & Rare Disease Studies
  • Medical Device Studies
  • Rescue Studies

6 reasons why Biotechs trust us

  • In-depth therapeutic & study expertise
    We match the right experience and people to your trial bringing you valuable knowledge from similar studies.
  • Extensive UK regulatory knowledge
    Gain the MHRA compliance expertise (IMP/medical device) you need to ensure your trial meets regulatory standards for the UK.
  • Collaboration and transparency
    Working collaboratively as an extension of your team, we engage quickly to understand your requirements and identify the most efficient and effective delivery options for your study.
  • Agile & solution-focussed
    As a medium size CRO we can act fast without excessive bureaucracy and genuinely dedicate ourselves to the shared success of your study .
  • Quality Assurance
    GCP and ISO trained staff and our ISO accredited Quality Management System ensure quality and compliance at every step.
  • Flexible & transparent costings
    Our ‘pick and mix’ service model allows our Sponsors to benefit from a tailored service. Transparency is important to us, our detailed costing breakdown ensures expectations and deliverables on both sides are agreed from the start.

Our sponsors enjoy working with us, and we do too.

"The most collaborative CRO I've worked with. PHARMExcel bothered to know us as a client and understands our studies inside out, making it an efficient and friendly partnership."

Prof Mark Lowdell, CSO INmune Bio Inc

"PHARMExcel’s passion for their projects, the flexibility shown by the team, combined with direct access to the CEO, sets PHARMExcel apart from other CROs."

Daniel Green, CEO and Sponsor Yaqrit

We take shared ownership in your clinical trial

Learn more about our successful CRO-Biotech partnerships

We’re here to help you bring your novel therapy to patients.

Let’s start a conversation