ELIQUENT Life Sciences
Niquette Channer is a highly experienced professional in quality and regulatory compliance within the life sciences sector. Currently serving as Principal Consultant at ELIQUENT Life Sciences since September 2024, as well as at Channer McKenzie, Inc. since April 2023, Niquette specializes in consulting, training, and audit support to ensure compliance with US FDA and global regulations. Previous roles include Senior Director of Global Internal Audit at Siemens Healthineers, Associate Director of Global Supplier Quality at BDBD, and Senior Manager of Global Quality Projects at Medtronic, showcasing a strong background in business process improvement, complaint management, and supplier quality. Niquette holds a Master of Science in Industrial Engineering/Engineering Management and a Bachelor of Science in Chemical Engineering from Northeastern University.
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ELIQUENT Life Sciences
We are expert consultants delivering the answers and solutions that life sciences innovators need to gain and maintain market authorization for their products. Our unprecedented assembly of regulatory leaders, industry experts, and technical specialists collaborate seamlessly to unlock excellence throughout the product lifecycle. We are the convergence of regulatory expertise and technical capabilities across the therapeutic landscape. From thought to finish, concept to commerce, and strategy to execution— ELIQUENT Life Sciences is the singular regulatory resource that clients around the world trust. ELIQUENT Life Sciences is comprised of five global consultancies working as a collective, coordinated regulatory team. The ELIQUENT team includes: VALIDANT: A full-service life science consulting firm providing strategy, execution, and ongoing support for a range of regulatory, compliance, and quality needs. GREENLEAF HEALTH: A leading FDA regulatory consulting firm that provides strategic and technical guidance to pharmaceutical, biotechnology, and medical device companies. DATAREVIVE: A regulatory consultancy firm with expertise to deliver CMC, preclinical, clinical, and GxP expertise to innovators seeking product approvals in major global markets. ORIEL STAT-A-MATRIX: A global leader in training and consulting for business process improvement, regulatory compliance, and quality management systems. IDEC: A regionally specialized regulatory guidance and end-to-end product support for pharmaceutical innovators seeking approval in the Japanese market. Together, ELIQUENT redefines regulatory consulting with a full-service approach and comprehensive solutions that bridge the spectrum of regulatory challenges. Learn more at ELIQUENT.com