
With decades of global experience, our team maps a path to seemlessly help you navigate complex regulatory landscapes.
Our founder, Eryn Corriveau, MS, RAC (CDA/US/EU), had a vision - high quality expert advice affordably administered to guide those who need it most - entrepreneurs, passionate scientists, and academics with an idea and an asset! With 3 decades of global regulatory experience, advice comes readily to our network of seasoned experts meaning our knowledge is your knowledge without swallowing your seed funding. It is from the core belief that adding value and partnering with early stage companies to provide real solutions and usable strategy should not be cost prohibitive, but rather practical and empowering, that FrontieRA was born. One blended hourly rate for every expert regardless of title, flat rate strategic plans with no hidden costs or change orders, openly leveraging the power of AI, and offering unlimited email access to the experts working on your project without additional fees are ways we are doing things differently to help you reach new heights.
We understand how important early drug development strategies are to the longterm success of your assets and offer in depth analyses, affordably priced, for the customers we value -- small biotech and startups who need to bring big ideas to fruition as timely and cost-effectively as possible. To launch your business we offer economically priced global regulatory strategy plans, scientifically-based investor decks, as well as full nonclinical/clinical development plans and gap analyses of existing datasets and more.
Are you further down your development path, have some data, perhaps some feedback from the FDA or scientific advice from EMA but now are unsure how to proceed? When you are facing what feels like an insurmountable roadblock, we take a holistic view of your situation and seek out the right pathway for what you need to achieve. We pride ourselves on creative, innovative, contemporary, and most importantly, science-based regulatory solutions that will give you credibility with any major regulatory body and the investment community.
If you are tired of your regulatory consultants just quoting guidelines, underestimating recent regulator initiatives to streamline drug development that you are convinced apply to your product, or are stuck and just not sure where to start, let us help breathe new life into your program!
Your success is our success.
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We are a global team, time zone agnostic. Connect wih us at any time! We will return your message within 48 hours.
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