The pathway to market is complex, but DLRC can simplify your journey. Operating from our UK, Germany, and US offices with over 1,000 years of combined experience, we collaborate with diverse clients, from top-five pharma companies to SMEs and start-ups. We develop and execute innovative phase-appropriate regulatory strategies to provide comprehensive support from very early in a product's lifecycle to post-licensing activities for medicinal products and medical devices.

Our team comprises consultant experts in non-clinical, CMC, clinical, and MedTech fields from pharmaceutical, medical device, and regulatory agency backgrounds. With a wealth of knowledge and experience, we have proudly served over 130 companies of all sizes and backgrounds in various regulatory jurisdictions.