Clinical services for drug discovery and development

We support clinical study development and delivery — across all phases of clinical trials globally — for rare conditions and diseases. We provide expert scientific and operational guidance throughout the drug development process to help you successfully deliver your clinical projects and bring potentially life-saving treatments to patients as quickly as possible.

Many of our clients work with innovative drugs or in rare indications where conventional clinical study protocols and pathways don’t always apply. In these rare and complex therapeutic areas, navigating the various stages of drug development and designing appropriate clinical studies can be challenging.

At TMC, we will guide you, as your partner with multidisciplinary service offerings and experienced personnel, throughout the drug development process — using our knowledge of rare diseases and expertise in clinical governance to ensure the successful clinical development of your product, including clinical trial design.

At the heart of our clinical services is our mission — indeed our passion — to support drug development solutions that improve patients’ lives. By accelerating clinical development timelines and maintaining a rigorous focus on quality, we ensure your clinical study is conducted timely and effectively, allowing your novel therapies for rare disorders and diseases to reach the patients who need them most.

Developing clinical study protocols for rare diseases

As a specialist clinical research organisation for rare disorders and diseases, we have extensive experience with clinical development in this area — particularly across our key specialisms of oncology, neurological disorders, respiratory diseases, haematology, ophthalmological conditions, neonatology, hepatology and nephrology diseases.

In the field of rare diseases, where patient populations are often extremely small, clinical study protocols must be carefully designed and adapted to the needs of each patient. Our experience in developing decentralised and hybrid clinical studies will ensure your trial not only meets regulatory requirements but also prioritises the patient.

Our clinical services include all aspects of clinical development. We’re committed to supporting you through every stage of conducting a clinical study. From the development of the initial clinical trial design and robust clinical monitoring programme to creating clinical study reports (CSR), we ensure the highest quality with a focus on patient safety, data integrity and regulatory compliance. We’ll also handle clinical project management and governance, facilitating data safety monitoring board meetings and ensuring compliance with complex international standards.

The perfect FIT for clinical development

We help you accelerate the clinical development of your drug and bring treatments for rare disorders and diseases to patients swiftly through our flexible, integrated and tailored services.

Flexible model 

Clinical research requires flexibility — particularly in the case of rare diseases, where trials often require a specialised approach. We’ve developed a close bond with our global network of trusted and highly skilled associates, enabling us to mould our business model to ensure the swift and cost-effective deployment of resources. Our clinical services are adaptable across all phases of your clinical study.

Integrated approach

From pre-clinical planning to final clinical study report submission, clinical development requires collaboration to ensure seamless progression. That’s why our people are your people. We support you throughout the clinical trial and drug development process, working in tandem with our regulatory, pharmacovigilance and medical teams to achieve the best possible outcomes for you and your patients.

Tailored solutions 

No two drug discovery and development programmes are the same — just as no two patients are the same. Our extensive experience in clinical development for rare diseases allows us to navigate complex regulatory processes and explore creative and effective solutions for clinical study protocols. This approach helps us conduct quick and successful clinical trials, accelerating your journey to market.

Get In Touch

Whether it’s creating an effective clinical trial design or maintaining clinical governance, we’re here to support your clinical development from start to finish.

Email our team today to discuss your requirements or contact us below. Together, we can ensure novel, life-saving therapies reach the patients who need them — faster and more effectively.