I specialize in regulatory medical writing, adeptly transforming intricate clinical data into clear, concise, compliant, and submission-ready documents tailored for sponsors, regulatory bodies, and health authorities. My expertise ensures that complex information is presented accurately and effectively, facilitating seamless communication and expediting the approval process.

With 5 years of extensive experience in medical communications for patients, primary care physicians, and a growing portfolio in regulatory writing, I develop and QC review regulatory documents that support drug development and approvals.

Previously, I’ve helped organizations in healthcare and life sciences communicate effectively with their target audiences through blog posts, white papers, journalistic reporting, conference coverage articles, case studies, e-books, research papers, web copies, and other marketing collaterals.  I’ve written 200+ deliverables for over 30 companies ranging from startups to well-established, including major brands and publications like Medscape, Healthline, Endocrinology Advisor, Cardiology Advisor, Medical News Today, WebMD, Health Union, Remedy Health Media, Everyday Health, MD Linx, and more. 

I’ve also developed content marketing assets in several therapeutic areas, including oncology, cardiology,  nephrology, endocrinology, gastroenterology, pediatrics, dermatology, infectious disease, ophthalmology, and psychiatry.

My expertise has given me the privilege to attend keynote events such as  the European Alliance for Personalized Medicine (EAPM) seminar in Belgium, Med-Tech awards in Malta, the BIO-Europe Spring Conference in Switzerland, the BIO-Europe Winter Conference in Germany, Global Health Awards UK, and the Reuters Pharma Conference in Philadelphia, USA. I’ve also attended several seminars and workshops both online and in person on regulatory affairs.

Fun facts: I combine left-brain analytical skills with right-brain creativity.

“Do you struggle with finding the right regulatory writer for your drug development process? I’m the regulatory medical writer you’ve been looking for.”