André Dias

Global Regulatory Affairs – eCTD Submissions Lifecycle Management

André Dias is a Global Regulatory Affairs Strategist with over 10 years of experience in pharmaceuticals, clinical research, and medical devices regulated by ANVISA. Currently serving as a LATAM Regulatory Affairs Consultant & Business Executive at OLERAH Consulting since 2019, they also hold a role at Tata Consultancy Services focused on eCTD Submissions Lifecycle Management. André holds a Bachelor of Pharmacy and a postgraduate degree in Regulatory Affairs, along with ongoing studies in Technology and a Data Science Certificate from IBM. Recognized for their expertise, they actively contribute to regulatory working groups and industry associations, driving compliance excellence and market access.

Location

São Paulo, Brazil

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