FinnBrit Consulting provides assitance to guide you through your drug development program beginning with preformulation and subsequent process design, development and manufacturing to the eventual launch of the finished medicinal product. We also provide assistance with issues relating to intellectual property, i.e., review of draft patents and expert witness assistance. Finnbrit Consulting also provides assistance with reviews associated with in-licensing, mergers and acquisitions as follows: viability of CMC programs, intellectual property review of formulations and Suitability of formulations for potential commercial manufacture.