TMC is a global clinical research organisation supporting small-to-medium biotech and biopharmaceutical companies through all clinical study stages — from Phase 0 exploratory trials to post-authorisation. 

As a full-service CRO, we understand the inherent challenges of the drug development process, particularly in the rare disease landscape, partnering with you to bring your treatments to patients rapidly and cost-effectively.  

Our in-house experts and network of highly skilled associates deliver a complete range of flexible, integrated and tailored services that span clinical development, consulting and functional execution for clinical studies and post-approval commercialisation to support market access and the long-term success of your product. 

Need strategic expertise to help you  

NAVIGATE THE EUROPEAN MARKET?

We can be your legal representative in the EU for clinical studies. 

Which drug development solution do you need? 

TMC Clinical 

Want to know how an orphan drug designation (ODD) can reduce your costs and extend your market exclusivity? Or get guidance on running decentralised versus hybrid trials?  

We support clinical development and delivery — across all stages of clinical studies — for rare diseases, providing strategic guidance to help you take advantage of incentive pathways and ensure your trial is conducted timely and cost-effectively. 

TMC Consulting  

If you want to quickly scale your clinical research operations, our consulting and functional service provider solutions integrate with your internal processes to give you specialised expertise where you need it most — without losing operational control. 

We offer strategic planning and functional execution across regulatory affairs, clinical development, medical services, pharmacovigilance and quality assurance. 

TMC Commercial  

Looking to successfully commercialise your products in the UK and EU — without a local legal entity or all the other complexities associated with entering new markets? 

By acting as your marketing authorisation holder (MAH), we ensure your product consistently meets the stringent safety, efficacy and quality standards required by regulatory authorities, reducing the time and cost of bringing it to market. 

TMC Clinical 

Want to know how an orphan drug designation (ODD) can reduce your costs and extend your market exclusivity? Or get guidance on running decentralised versus hybrid trials?  

We support clinical development and delivery — across all stages of clinical studies — for rare diseases, providing strategic guidance to help you take advantage of incentive pathways and ensure your trial is conducted timely and cost-effectively. 

TMC Consulting  

If you want to quickly scale your clinical research operations, our consulting and functional service provider solutions integrate with your internal processes to give you specialised expertise where you need it most — without losing operational control. 

We offer strategic planning and functional execution across regulatory affairs, clinical development, medical services, pharmacovigilance and quality assurance. 

TMC Commercial  

Looking to successfully commercialise your products in the UK and EU — without a local legal entity or all the other complexities associated with entering new markets? 

By acting as your marketing authorisation holder (MAH), we ensure your product consistently meets the stringent safety, efficacy and quality standards required by regulatory authorities, reducing the time and cost of bringing it to market. 

‘Thank you… and I must take a moment and specifically let you know how well-regarded you are here and how grateful we are to be working with you.’
Chief Operating Officer, global biotech client
‘I cannot even begin to thank you for all your hard work over the last few weeks driving toward database lock. Every time there seemed to be a light at the end of the tunnel, we added another hurdle! You handled absolutely everything we threw at you brilliantly!’
Head Clinical Project Manager, biotech client
‘Very happy to have you and the TMC team on our side as our partner! This is a really important project for us, and I can’t think of anyone else I would want in my corner — thank you!’
Chief Scientific Officer, global biopharma client
‘I would like to thank you and all the TMC team for a very successful collaboration. The quality of service received contributed to the project outcomes, with every step of the process delivered seamlessly and professionally.’
Research Project Manager, global pharmaceutical client
‘Your support and partnership are greatly appreciated and have been instrumental in delivering this milestone.’
CMO, global biotech client

If you want to maximise your product’s market potential and bring your treatment to patients faster and more cost-effectively, TMC is the CRO for you. Contact our team today to find out more about our drug development solutions and see how we support you through all phases of clinical research.