Brian Scogland joined Halloran Consulting Group in 2014. He has more than 10 years of experience in regulatory affairs and quality system development. he has experience in creating and implementing quality systems in the medical device industry that ensures compliance with FDA’s quality system regulations. He has also led organizations through FDA inspections with successful outcomes.
Prior to joining Halloran, Scogland was the regulatory affairs manager for lifeIMAGE, where he developed robust practices and procedures to ensure products comply with FDA regulatory requirements. While at lifeIMAGE, he managed documentation control, supplier controls, CAPA process, internal audit programs, complaints, and Medical Device Reporting (MDR). Prior to lifeIMAGE, he held various positions at Boston Scientific and Caliper Life Sciences.
Scogland earned a Master of Business Administration and Master of Science in Management from Babson College. He earned his Bachelor of Science in Management with a concentration in Management Information Systems from Rensselaer Polytechnic Institute. Brian also holds his Regulatory Affairs Certification (RAC).
Brian can be reached at [email protected].