Ossie Milanov, B.A.
Quality & Regulatory Project Manager
Ossie Milanov is a regulatory and quality expert. She has worked with many start up medical device companies over the years. She has experience in establishing, implementing and maintaining a QMS; in particular effective and compliant Risk Management and Post Market Surveillance. Ossie has experience in preparing Regulatory Strategies and submissions for the FDA, EU and WHO. She has successfully participated in FDA, EU and WHO audits as the lead point of contact.