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Gus Kobrin has over 30 years of experience in the
medical device manufacturing industry. Regulatory Affairs and
Regulatory Compliance experience built upon a foundation of
engineering testing. Mr. Kobrin has diverse, hands-on experience
with international and domestic product registrations of all medical
device classifications; regulatory inspections; quality system
development; auditing, and project management. Gus Kobrin is a
Notified Body Auditor, Certified Quality Auditor (CQA) and Certified
Regulatory Affairs professional (RAC). Gus Kobrin is bi-lingual,
Spanish-English.
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