About me
Aysha Rana, PharmD, MS is a Regulatory Affairs professional with 7+ years of global experience spanning pharmaceuticals, biologics, and medical devices. A recent graduate of Northeastern University’s Master’s in Regulatory Affairs program, she has led regulatory strategy, eCTD submissions, and compliance initiatives aligned with USFDA, EMA, and EU MDR standards. Aysha has successfully supported product approvals across the U.S., EU, ASEAN, WHO and CIS markets. Passionate about innovation and patient safety, she continues to contribute to regulatory excellence through cross-functional collaboration and global regulatory intelligence.
