Director, Regulatory and Clinical Development, Alira Health
Tabatha Bourgois is a regulatory and business development expert with over a decade of experience in the Pharmaceutical and MedTech industries. In her current position at Alira Health, she leads business development efforts in regulatory and clinical consulting, helping sponsors achieve successful market entry in the EU and US. She excels in building long-term client relationships, developing competitive strategies, and managing cross-functional teams for multi-practice & go-to-market projects. Tabatha specializes in development pathways for drug products, biologics, and medical devices, with expertise in EU MDR, IVDR, and FDA regulations
With a background in materials science from EEIGM Engineering School in France, she has contributed to innovative projects in drug delivery, medical devices, and biomaterials. She is also a co-author of several patents in the medical field, reflecting her dedication to healthcare innovation.
