At Tricentric, we boast a huge range of services, allowing us to bring our clients comprehensive services to support their clinical endeavours. We’re proud to bring flexibility and attention to detail to our work, which is why we’re able to find unique solutions, be proactive and spot issues before they impact your project. This approach makes delivery as simple and efficient as possible ensuring you’re not wasting time or funds on poor administrative decisions.
We specialise in regulatory consulting, investigator contracting and budget negotiations for clinical research sites across the UK. This means you’re free to focus on the things you do well knowing that you’re getting your work done while meeting regulatory standards at the best possible price.
Thanks to our extensive experience, we’re able to service our clients’ unique needs. As a small to medium-sized CRO, medical device, pharmaceutical or biotech company, we understand that you often have stricter timelines and need to be able to work quickly. We’re a nimble team with the necessary background to provide the right kind of support.
We’re passionate about fostering open and honest communication with our clients so that we have a comprehensive understanding of what you need and how we can best provide it. This allows us to get into action right when we’re needed.
The experts at Tricentric are committed to developing and maintaining excellent working relationships to ensure we achieve successful and rewarding outcomes for our clients, the people they work with and the community at large.
We’re a friendly, approachable team with the background and specialised knowledge needed to support a range of sectors and therapeutic areas. From Phase 1 to Phase 1V, Post Launch (Real World Data) studies, either drug or medical devices and everything in between, think Tricentric, think Success.
If you would like to know more about us and our management services and how we can help your clinical trial, feel free to send us a message with your queries.