Profile Summary
Mohammed H.
I am a CER (Clinical Evaluation Report) specialist and technical writer with experience in developing clear, accurate, and evidence-based scien...
Rita H.
I am a Regulatory Affairs and Quality Assurance consultant with 15+ years of experience in the medical device and pharmaceutical industries, an...
Jeroen W.
Since 2011, I have been working in the cardiovascular medical device field, with experience as both a Clinical Project Manager and a Medical Wr...
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PANAGIOTA A.
Highly accomplished Physicist, Academic Expert, and Senior Scientific Researcher with over 20 years of experience in higher education, scientif...
Gabriela S.
Regulatory Affairs professional with ~7 years of experience across medical devices, IVD, and chemical compliance, specialising in EU MDR/IVDR, ...
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Kay G.
Industry consultant/contractor with extensive hands-on experience assisting offshore and domestic clients in bringing molecules to market. Sub...
Dr. Denard J.
I am Joseph, provide research and technical documentation support focused on Medical Device Regulation (MDR), regulatory requirements, and medi...
Dr. Adam S.
Former university professor & PhD-qualified academic consultant with 12 years of experience delivering publication-ready dissertations, the...
Dr. Rupak D.
Materials Metric specializes in advanced material testing and characterization, serving clients across industries including pharmaceuticals, ae...
Dr. Dr. Srinivas V.
I am a PharmD graduate currently working as a Clinical Research Associate (CRA) in a CRO. I have experience in clinical research...documentation, protocol and ICF review, scientific writing, literature research, and manuscript preparation and publication...
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Our T&C include a default confidentiality clause that protects your IP and NDA for added protection.
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EU MDR consulting services needed$550.00
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