DLRC is an award-winning consultancy team of over 80 highly qualified and experienced regulatory affairs professionals, operating from our strategically located offices in the UK, Germany, and the US. With a deep commitment to excellence, we are dedicated to helping our clients navigate the complex regulatory landscape of the life science industry.

At DLRC, we collaborate with a diverse range of clients, from Top 5 Pharma companies to SMEs. We develop and execute innovative phase-appropriate regulatory strategies to provide comprehensive support from very early in the lifecycle of a product right through to post-licensing activities, for both medicinal products and medical devices.

Our team comprises consultant experts in non-clinical, CMC, clinical and MedTech from pharmaceutical, medical device and regulatory agency backgrounds. With a collective wealth of knowledge and experience, we have proudly served over 130 companies of all sizes and backgrounds in various regulatory jurisdictions. Our partnership has enabled them to achieve success in both their strategic and operational development objectives.

DLRC's hallmark is our extensive expertise, agility and integrity. We are a global team motivated by solving complex challenges and that excels in interactions with both clients and regulators. Our flexible and efficient working approach means can deliver for our clients whether it be agile, standalone solutions or end-to-end regulatory outsourcing solutions for our clients.

Our unwavering commitment to excellence has earned us numerous accolades and industry recognition, solidifying our reputation as a trusted name in the life science industry.

DLRC is more than a regulatory consultancy group; we are your gateway to unmatched regulatory success.