TMC Pharma provide a core range of services to the international market

We support your journey through global regulatory pathways — navigating efficiently from initial drug discovery through development and avoiding unnecessary delays to gain rapid approvals for clinical trials and marketing authorisations.

We provide proactive pharmacovigilance solutions for the routine and ad hoc monitoring of the safety of your product, whilst ensuring your regulatory compliance — from the first moment it’s given to a patient and throughout the drug life cycle.

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.

We bridge the gap between clinical development, regulatory compliance and market access, supporting your journey throughout the drug life cycle by offering specialised medical services that ensure your product not only meets safety and efficacy standards but is also optimised for commercial success.