Patrick is our industry expert having spent over a decade in regulated industries such as pharmaceuticals, radio-pharmaceuticals, pharmacopoeia, and medical devices. He is a Credentialed / Certified Lead Auditor in EN ISO 19011:2011 - Quality Management Systems, ISO 13485:2016, EN ISO 13485:2016, and FDA QSR; 21 CFR, Part 820. He is also an industry veteran, keynote speaker of 25 years in Global Sourcing, Procurement and Supply Chain Management. 

He is pivotal in ensuring the compliance and quality standards of our research materials and supply chain ensuring our customers have access to the highest purity and quality items.