Meet Robert Packard, a medical device quality and regulatory expert with over 20 years of industry experience and 10+ years in biotech manufacturing.
He’s led Quality and Regulatory Affairs at multiple startups, co-founded a laparoscopic imaging company, and served as a lead auditor and instructor for a major Notified Body. Today, he helps startups achieve 510(k) clearance, CE Marking, and global compliance—while building a fully remote consulting team.
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