Tanya Rackstraw

Tanya has more than 20 years of experience in the pharmaceutical industry, both in regulatory affairs and medical writing. 

She has developed extensive expertise in pharmaceutical regulation, licensing, and documentation across a wide range of therapeutic areas and medicinal product types. Tanya’s particular strengths lie in regulatory strategy, European Union orphan drug designations, centralised procedure marketing authorisation applications, and UK regulatory procedures. During her career, Tanya has worked across a variety of organisations, including a national regulatory agency, a pharmaceutical company, regulatory affairs consultancies, and a medical writing consultancy. This breadth of experience has given her a well-rounded perspective on regulatory processes across the industry. 

Tanya holds a Master’s Degree in Applied Biology from Birkbeck College, University of London and a Bachelor of Science in Biology from the University of Sussex.