We provide regulatory and scientific expertise to deliver an effective and efficient framework for your regulatory submission process. This includes both pre and post-registration activities so that you maximise value throughout your product supply chain.
We understand that you will want to create the most efficient and cost effective plan for your regulatory submission. Our dedicated team of talented scientists, regulatory experts and motivated project managers will ultimately work with you to create a Common Technical Document (CTD) for submission against the Medicinal Products Directive.
Broughton Laboratories provides regulatory consultancy services to the following industries: