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About

Barbara Alves is a Regulatory Affairs Specialist at BD Medical – Pharmaceutical Systems. She provides guidance on the regulatory requirements to be considered in the design input specifications of new products and manages regulatory documentation to support biopharmaceutical partners in their drug device combination registration process worldwide. Ms Alves holds an MSC and a university degree in regulatory affairs.
Prior to joining BD four years ago, she worked in regulatory affairs for pharmaceutical companies for 15 years.

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