Validant
Andrea Corti is a seasoned pharmaceutical technology and compliance consultant with extensive expertise in FDA and EU current Good Manufacturing Practices (cGMPs). Engaged with Corti Consulting since June 2017, Andrea advises the pharmaceutical and biotechnology sectors on regulatory compliance, remediation strategies, and preparation for FDA/EMEA inspections. Additional roles include Associate Consultant at NSF International and Senior Quality Assurance Consultant at Validant, focusing on regulatory inspection readiness and remediation plans. With a robust background at GSK, Novartis Vaccines, and Chiron Corporation, among others, Andrea has managed quality assurance operations, new platform introductions, and compliance with industry standards throughout a career spanning over four decades. Andrea holds a degree in Pharmacy from the Università di Siena and is a graduate of Industrial Chemistry from the Industrial High School T. Sarrocchi of Siena.
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Validant
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Validant is a full-service life science consulting firm serving developers and manufacturers of pharmaceuticals, biologics, medical devices, and diagnostics worldwide. We partner with these companies to ensure safe and reliable access to life-saving healthcare products, facilitating their efficient, compliant progression from preclinical and clinical phases through to manufacturing and distribution—and optimizing quality at each step. Our platform brings together leading specialists in each facet of the product lifecycle, and we have curated an extensive and diverse global network of consultants to help execute strategies worldwide. Because of this, Validant is able to deliver our breadth of consulting, execution, and support services in the right place, at the right level, and in the right combination to meet your exact need. We've empowered hundreds of clients – from start-ups to the largest global leaders – to efficiently navigate regulatory, compliance, and quality complexities. How can we help you?