Pedro Ferreira

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ValGenesis, Inc.
Pedro Ferreira currently leads the Consulting’s Quality Risk Management division at ValGenesis. In this role, he is responsible for delivering world-class validation, quality, risk, and knowledge management consultancy services spanning all phases of drug development and commercialization. Pedro has over 10 years of experience in the pharmaceutical and chemical industries. Over the course of his career, he has held positions ranging from quality control and assurance of pharmaceutical products to the quality management of computerized systems and continuous improvement projects under the GMP scope. Pedro holds a licentiate degree in pharmacy from the Polytechnic Institute of Lisbon and a master’s degree in biotechnology from the NOVA University of Lisbon. He has been an ISPE member since 2021.

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Pharmaceutical continuous manufacturing (CM) is recognized as a key process intensification technology, with investment expected to rise in the coming years and the focus shifting toward biologics. This article provides a review on the current state of CM implementation, offers insights into life cycle management and regulatory aspects, and explains how a data- and knowledge-centric approach...