Profile Summary
Michael L.
I am an accomplished professional with a PhD in Optoelectronics and Laser Systems, along with an Executive Certificate in Innovation Management...
William T.
Experienced Technical Writer and Laboratory Scientist adept at managing and executing multifaceted projects within stringent timelines. Profici...
Mohan M.
Over 35 years of broad experience as Engineering professional…Medical Device Product Regulatory Requirements, Product Design, Project Managemen...
Michael B.
30+ years experience in MedTech. NICE MedTech Early Technology Assessment (NICE MetaTOOL) facilitator. Proven record in getting great technolog...
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...
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Hana A.
Regulatory submission to Health Authority, GDPMD, QMS, ISO 13485, GDP, Post market surveillance and audits.
Pragatheeshwaran N.
Experienced in Medical device Post Market Surveillance (PMS) and process improvement. Familiarity with USFDA (21CFR Part 820, 806 and 803), QMS...
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. ...
Krishnakant S.
Regulatory Affairs and Toxicology Expertise: 1. Proficient in toxicological hazard assessment and human risk evaluation for product safety acro...
Ayoub B.
I am a trilingual Biomedical Engineer (French/English/Arabic) with dual academic training from UTC Compiègne (France) and ENSAM Rabat (Mor...
Dr. Somnath Swami V.
Researcher with expertise in solubility enhancement and formulation development of pharmaceutical compounds, focusing on the use of mesoporous ...
Devin M.
I help medtech companies design, assess, and improve quality systems to ensure regulatory compliance, streamline development, and prepare for a...
Dr. Mohsen M.
I’m a biomedical engineer (PhD) with over 15 years of cross-functional experience in medical device development, neurotechnology, and regulator...
Dr. Alexandra A.
With 16 years of industry and academic experience combined in the medical device and interventional oncology fields, I am passionate about alig...
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Kathleen D.
👩🏻💼 Who I Am: Seasoned QMS and Compliance consultant dedicated to helping organizations achieve operational excellence...
Wim V.
I am an experienced independent consultant specializing in clinical research management for medical devices, with a focus on EU MDR compliance,...
Dr. Karla R.
biomedical engineer and AI consultant with 10+ years of experience in research, development, and implementation of digital health solutions, me...
Kristen D.
Innovative executive in clinical operations and regulatory affairs with successful experience in start-ups, hospital & CROs, private equity...
Mohamed H.
I am a Clinical Research Professional with over 13 years of global experience in clinical trial management, medical writing, and regulatory sub...
Woodrow S.
I am a Certified Quality Engineer and ISO 13485-trained Lead Auditor with a background in biomedical engineering and hands-on experience leadin...
Dr. Diana K.
I’m a medical doctor (OB/GYN), bioinformatics & data science graduate, and experienced medical writer with 4+ years in clinical trial suppo...
Prafullakumar P.
I am medical devices regulatory affairs professional having expertise in following points - Author, Reviewer of Global Regulatory Technical Doc...
Dr. Sevgi Ç.
14+ Years academic experience, expert in scientific writing, paraphrasing and biomedical documentation. Published author in SCI journals and b...
Dr. Patricia D.
I am a Pharmacist with a PhD in Sciences Applied to Health Products (UFF) and a Master’s degree in Pharmaceutical Sciences (UFRJ), combining ov...
Dr. Amin H.
I’m a PhD-level Medical Writer and Biomedical Engineer with over 10 years of experience in clinical research, scientific writing, and regulator...
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EU MDR consulting services needed$550.00
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