
Naveed A
Level 2
Medical Device Regulatory and QMS Consultant
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Medical Device Regulatory and QMS Consultant
Consultants • Freelance
Nov 2022 - Present • 4 yrs
Provide medical device regulatory and QMS consulting services to medical device and IVD companies, supporting regulatory compliance, quality systems, and technical documentation. Experienced in FDA registration and listing, 510(k), EU MDR, UKCA, ISO 13485, ISO 14971, technical documentation, risk management, CER, IFU, SOPs, validation, CAPA, SCAR, audits, and regulatory submissions. Deliver practical, accurate, and audit-ready documentation tailored to client and product requirements.
95 Reviews
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chesterlp

Portugal
Naveed gave a clear and well-referenced EU MDR review of our Class I device and the companion app. He was responsive, open to revisions, and answered all our follow-up questions. Recommended for MDR guidance.
jas_rav1985

Verenigde Staten
Second time working with Naveed and again he went above and beyond to help. Very professional and knowledgeable. Highly recommend
Reactie van de freelancer
jas_rav1985

Verenigde Staten
Really great guy. Knowledgeable and willing to go the extra mile to help out. Will be hiring him again
Reactie van de freelancer
dolivierp

Argentinië

ilanohayon443

Verenigde Staten



