I lead global regulatory and clinical development strategy through from idea, into First in Human clinical trials, through clinical development, then marketing application and launch.
With more than 20 years development experience I have partnered with clients to develop their scientific storyline for regulatory authorities, to derisk their development programs, and ensure smooth market entry.
Wherever you are on your drug development journey; as a biotech – whether you’re still forming your team or seeking funding – or putting together your first marketing authorization submissions – I can jump into your project and apply my deep industry and regulatory expertise to optimize your development opportunity.