Ivanna Velilla
Ivanna Velilla is an MBA with more than six years of experience in operations, strategy, and regulatory environments, with a strong focus on medical device regulatory documentation and process optimization.
About Ivanna Velilla
She specializes in regulatory documentation management, workflow standardization, and compliance with INVIMA requirements, as well as international registration frameworks. Velilla has led regulatory operations and business strategy initiatives, designing and implementing systems to automate and standardize regulatory processes, maintain high-precision documentation for INVIMA and UDI-DI registrations, and coordinate activities between manufacturers, distributors, and regulatory authorities. In her role at Pure Global, she supports regulatory submission projects in Colombia, coordinating timelines, overseeing deliverables, and ensuring that documentation meets applicable regulatory standards.
Her background also includes senior leadership roles in marketplace management and large-scale project execution. She holds an MBA from Universidad de los Andes and a degree in Economics from Pontificia Universidad Javeriana.