Profile Summary
Manoj Krishnaa S.
I help clients to define the medical device documents and align with Regulatory aspects. Works with small business owners and entrepreneurs. T...see more
Michael B.
30+ years experience in MedTech. NICE MedTech Early Technology Assessment (NICE MetaTOOL) facilitator. Proven record in getting great technolog...see more
Eric D.
Over 25 years of experience in all facets of clinical research including with a focus on early phase medical devices and combination products. ...see more
Krishnakant S.
Regulatory Affairs and Toxicology Expertise: 1. Proficient in toxicological hazard assessment and human risk evaluation for product safety acro...see more
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Hana A.
Regulatory submission to Health Authority, GDPMD, QMS, ISO 13485, GDP, Post market surveillance and audits....see more
Pragatheeshwaran N.
Experienced in Medical device Post Market Surveillance (PMS) and process improvement. Familiarity with USFDA (21CFR Part 820, 806 and 803), QMS...see more
Haralabos P.
Working as a medical translator for the past 19 years (9 years full time), I have translated a wide range of biomedical documents including med...see more
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EU MDR consulting services needed$550.00
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