TRP's founders have a proven track record in all phases of regulatory documentation production and submission. Our substantial experience allows us to provide quality and efficient service in a timely manner. We are flexible and adapt to our clients' needs.
Irisha Johnson, RAC
With over 15 years of professional experience in regulatory environments, Irisha has been on the front lines of the ever changing regulatory landscape of Covance Inc, GlaxoSmithKline, and Gilead Sciences. Transitioning to a Regulatory Submissions Publisher at the onset of FDA's electronic initiative, Irisha is a subject matter expert in the field of electronic submissions. She has managed the publishing and successful submissions of various types of US and Canadian submissions, including NDA's, INDs, CTAs, sNDA's, and sNDS's with a specialization in Chemistry Manufacturing and Controls. She has helped to implement electronic processes within her organizations and transitioned over 100 applications from paper to electronic with regulatory authorities. Irisha holds Associates of Applied Science in Computer Information and her Bachelors of Science in Business Management. Please learn more about her experience via LinkedIn.