Ritika Sharma

Ritika Sharma is a Senior Regulatory Affairs Specialist at Abbott since August 2023, previously serving as a Regulatory Affairs Specialist at Formlabs from January 2021 to August 2023, where key contributions included authoring a 510(k) submission and supporting EU-MDR audits. Ritika's expertise encompasses building regulatory files, preparing global submissions, and supporting technical documentation for product registrations. Earlier experience includes leading ISO 13485 and 21 CFR 820 gap analyses at the University of Southern California, interning in quality and regulatory affairs at Philips, coordinating clinical research for the "All of Us" NIH program, and working as a Pharmacovigilance Specialist at PAREXEL. Ritika holds a Master of Science in Regulatory Science from the University of Southern California and a Bachelor of Dental Surgery from Panjab University.