Profile Summary
Dr. Leon S.
With over 10 years of scientific and biotech experience across a range of fields, I can help you build your project’s theoretical foundation an...
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...
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...
Dr. Ark K.
I am a PhD-qualified molecular biologist with over 20 peer-reviewed publications and scientific books. For the past 8 years, I’ve worked in the...
Dr. Umadevi R.
A Seasoned Medical Writer and Regulatory Affairs professional with a Ph.D. and extensive expertise in authoring high-impact clinical and regula...
Deepa K.
I’m a passionate **Biochemistry postgraduate** with over **10 years of hands-on experience in Research & Development**, driven by a deep cu...
Anil I.
I am a Medical Device Quality, Regulatory, and Validation Specialist with 8+ years of experience at Philips, Johnson & Johnson, Medtronic, ...
Sohanur R.
Pharmaceutical quality and compliance specialist with over 15 years of experience in sterile manufacturing environments. Holds a Master’s degre...
Braden T.
I have 10 years of experience in research and evaluation. I co-own Final Test Health Research where we mostly support clients seeking FDA clear...
Henvi P.
I am a Bachelor of Pharmacy graduate and a QA Executive at a medical device company specializing in orthopedic products. With hands-on experien...
Dr. Alexandros P.
Biomedical Data and AI professional with 12+ years of experience in biostatistics, epidemiology, and real-world evidence. Ph.D. in Biostatistic...
Wim V.
I am an experienced independent consultant specializing in clinical research management for medical devices, with a focus on EU MDR compliance,...
Dr. Anand kumar P.
ISO 42001 ARTIFICIAL INTELLIGENCE SYSTEM IMPLEMENTATION | ISO 13485 FOR MEDICAL DEVICES | ISO27001 FOR MENTAL HEALTH PRODUCT | HIPAA GDPR COMPL...
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...
Deepak D.
Highly motivated Regulatory Affairs professional with strong expertise in U.S. FDA 510(k) submissions, Indian import licensing (CDSCO), ISO 134...
Sobhan M.
Solid 10+ years of Experience in AI/ML/Data-Driven Research and Development for Clinical Decision Support (CDS) and Software as Medical Device ...
Patrik S.
I currently work as a Clinical Research Lead in a Neurotech startup specializing in movement-based therapy and fNIRS. My role encompasses clini...
Setareh Z.
I am a Biomedical Sciences student with hands-on experience in hospital diagnostics, laboratory research, and clinical environments. I hold cer...
Yanka R.
I’m a biomedical innovation professional with a background in materials engineering, medical device development, and clinical translation. As a...
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...
Dr. Evrim Atılay T.
Throughout my career, I have led cross-functional teams in pharmaceutical development across leading companies in Turkey. I have successfully d...
Prafullakumar P.
I am medical devices regulatory affairs professional having expertise in following points - Author, Reviewer of Global Regulatory Technical Doc...
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EU MDR consulting services needed$550.00
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