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PHARMExcel

“Together we make it happen”

PHARMExcel is a full-service Contract Research Organisation (CRO) providing a flexible and innovative approach to clinical trial delivery.

The company offers in-depth knowledge and experience of the clinical research environment, particularly in the UK, and has a network of regulatory, and other industry associates, allowing us to provide a global reach.

Pragmatic approach to clinical trials

Partnerships

We pride ourselves in “doing the right thing” along with our pragmatic approach to trial set up, management and delivery. We like to see ourselves as an extension of your organisation and ensure we work alongside you for the duration of the study. Partnerships are hugely important to us. As our motto says “Together we make it happen!”

Dedicated to delivering results

Because we are a small CRO we really dedicate ourselves to our customers. We are able to engage quickly to understand your requirements (we really do listen!) and identify the most efficient and effective delivery options for your study. You will not be weighed down by internal bureaucracy and decisions are made quickly and promptly.  This results in quicker start-up times for you, whilst still ensuring high-quality outputs; hence most of our work comes through repeat business and recommendations.

Our services

Whatever the size and scope of your project, each receives the same level of attention to detail and commitment to ensure a high-quality service, delivered within budget and to the timelines agreed with you.

 

We allow you the option to simply choose those services that you require in order to support your trial. This may range from assistance with protocol development or clinical trial regulatory submissions, through to writing your end of study report. Or you may require our full service. The choice is yours.

Our Values

At PHARMExcel we are driven by our four core values;

  • Honesty and Integrity -We create partnerships whereby honesty, integrity and trust is reflected in all we do.
  • Team Work-We work together to create an environment whereby cooperation, respect and professionalism is at the forefront of what we do
  • Quality-We manage and deliver all our projects through experience, expertise and ensuring compliance
  • Passion-We empower our staff through accountability, engagement and continuous learning

Our Mission Statement is to:

  • Listen to your needs and tailor the service delivery to your requirements
  • Ensure we provide innovative and pragmatic approaches to clinical trial delivery, ensuring your expectations are appropriately managed
  • Deliver your study on time, on budget and in compliance with applicable guidelines and regulations
  • Provide transparent and honest communication throughout the duration of your project
  • Ensure flexibility and out of scope work is promptly managed
  • Ensure quality in all aspects of work
  • Learn from all our project deliverables to ensure we can enhance our performance and ensure continual process improvement.

Why choose PHARMExcel?

We believe our staff are our greatest asset and we work hard to ensure all staff feel valued. We believe valued staff provide the best outcomes for our clients. At PHARMExcel, our instilled values incorporate honesty, quality, passion and customer focus, which is the key to success when working with our clients.

Everything we do is based on teamwork. Over the past 10 years we have built a solid company culture centred around our core values, respectful interactions and partnerships. Our staff enthusiasm and professionalism spans the organisation, which is reflected in the way we develop our client relationships.

Our flexible and innovative approach to trial delivery means we have the capabilities to manage small, simple studies that require a tailored ‘pick’ of our services, through to large, multi-centred, multi-country projects utilising our full-service. We have the expertise and systems to manage all clinical operations on your behalf, from early protocol development through to regulatory and ethics submissions, site selection and set up, project management, risk adapted monitoring, clinical study pharmacovigilance, data management & biostatistics, trial master file management and study close-out.

We work with a variety of clients including large pharma, medtech, small biotechs start-ups and academic institutions. One of our core values is our commitment and approach to your trial.  All our clients are treated the same, regardless of size or scope of work.