"We engaged Broughton to support our CMC activities for multiple investigational products. Their scientific expertise and structured regulatory approach aligned to our complex submissions. They operated as an extension of our internal team with their reliable and responsive and approach. It’s rare to find that level of client-focused partnership.’’

CMC Director, Mid-Sized Pharma Company

"Broughton’s ability to guide us through UK and EU regulatory pathways was invaluable. We needed high quality pharmaceutical development to support our regulatory submissions their team delivered with precision and pace. Their MHRA experience and attention to detail gave us the confidence we needed for critical submission milestones."

VP Regulatory Affairs, Global Pharmaceutical Company

"We needed a high-quality lab partner to handle release testing for multiple product lines across global markets. Broughton’s GMP compliance, streamlined onboarding, and LabHQ data platform helped us accelerate batch release timelines while maintaining quality. They’ve become a key part of our commercial operations."

CEO, US-based Pharma Company