Top Freelance European Medical Device Regulation (MDR) Experts For Hire

Dr. Ahram Q.

Expert Life Science's Researcher, writer, and Consultant
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USD 50/hr
MPhil in Bioinformatics
Pakistan

My professional background is to technically write the Scientific content, assess the researcher in research work related to Bioinformatics and...

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USD 50/hr
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Dr. Kurtulus G.

Expert with 10+ Years of Experience in Medical, Scientific, Technical and Regulatory Writing
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USD 100/hr
Ph.D. Biotechnology
United States

I am a freelance medical, scientific, and technical writer with high-quality researches at Harvard Medical School proven by research papers pub...

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USD 100/hr
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Dr. Sergio P.

MDR Consultant / CER writer
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USD 55/hr
Masters program about drug development
Spain

I have more than 6 years experience (research and pharmaceutical industry) with a long track of success. My years as a researcher provided me ...

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USD 55/hr
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Dr. Nare S.

More than 10 years of experience as Regulatory Affairs Specialist, Medical and Scientific Writer, Clinical Trial Consult
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USD 50/hr
PhD in Pharmacy
Armenia

My science qualification is a Ph.D. in pharmaceutical science. My writing qualifications: - Writing in the Sciences Certificate (Stanford Unive...

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USD 50/hr
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Dr. Dimitrios K.

Medical Writer & Market Research Consultant | Delivering Clear, Concise, Actionable Insights in Pharma & Biotech
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USD 60/hr
Ph.D.
United States

I'm a Freelance Medical Writer and Market Research Consultant. I provide Innovation Consulting, Market Research, and...Medical Communication services, including competitive intelligence, clinical trial materials, and study publications...

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USD 60/hr
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Dr. Muhammad M.

Data-Driven Scientist Specializing in Comprehensive Data Analysis and Scientific Writing for Advanced Research Projects
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USD 30/hr
PhD
Pakistan

Hello and welcome to my freelance profile! I am an accomplished Data-Driven Scientist with extensive expertise in comprehensive data analysis a...

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USD 30/hr
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Dr. Diksha V.

Researcher & Writer with 11+ years of experience in biotechnology, biomedical, bioinformatics and product developmen...
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USD 100/hr
PhD
India

I am a doctorate in life sciences with an experience of over 11 years in the academic and corporate sector. I have managed projects focusing o...

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USD 100/hr
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Madhu S.

Quality and Regulatory Affairs professional | Expert in CE marking, EU MDR 2017, FDA submissions & lead auditor ISO1...
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USD 30/hr
Advanced PG Diploma in CR & Regulatory Affairs (APGDCR-RA)
India

Over 7 years’ experience in Quality and Regulatory Affairs, and technical submissions for a range of medical devices, including Orthopaedics, S...

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USD 30/hr
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Nida A.

Experienced MDR and FDA certified CER/Technical File Writer with 7+ years of experience with multinational industries
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USD 50/hr
Law (LLB Honours)
Pakistan

An experienced clinical research and medical device Technical file writer who has certified on MEDDEV 2.7/1 Rev#4 documentation, EU MDR 2017/74...

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USD 50/hr
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Lisa R.

REGULATORY AFFAIRS - Medical Device - Biotech - Dietary Supplement - Pharma
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USD 200/hr
Certificate of Regulatory Affairs , Dietary Supplements and NHP
Australia

Highly motivated Product Formulation Expert and Regulatory Affairs Expert in the following fields: Medical Devices ,Pharmaceuticals ,Dietary Su...

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USD 200/hr
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Adam F.

exFDA Investigator / expert in Medical Device & Combination Product design, manufacturing, and compliance
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USD 200/hr
Bachelors of Science in Biochemistry
Switzerland

I performed inspections and premarket approvals for FDA for 7.5 years. I am now a Senior Consultant operating out of Switzerland. I operate a...

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USD 200/hr
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Danielle K. B.

M.D. | Clinical Research Professional | Medical Device | Pharmaceutical
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USD 60/hr
Medical Degree (MD)
United States

I am a clinical research professional with 6+ years of experience in the various therapeutic areas and industries including Respiratory, Anesth...

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USD 60/hr
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Joshita M.

Biomedical Engineer, CMU | Product Manager & Medical Writer | Expert in Clinical Research with 9+ years of experienc...
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USD 30/hr
MS - Biomedical Engineering
Netherlands

A passionate researcher, with a Master’s degree in Biomedical Engineering from Carnegie Mellon University (USA), I have 9 years of product deve...

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USD 30/hr
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Girish H.

Freelance Medical Writer / Regulatory Expert in Medical Device with 16+ Years of Experience (EUMDR, ISO 13485, FDA510K)
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USD 90/hr
B.Pharmacy
India

An accomplished, versatile, results-oriented clinical research professional with over 16 years of experience in the Pharmaceuticals & M...

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USD 90/hr
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Dr. Alex L.

Former academic, medical devices regulatory affairs consultant, specialising in clinical and performance evaluation.
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Doctor of Philosophy (PhD) Haematopoetic Stem Cell Gene Therapy
United Kingdom

Qualifications: MBiochem Molecular and Cellular Biochemistry, Oxford University PhD Haematopoetic Stem Cell Gene Therapy, University of Manches...

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Dr. Pavel O.

AI engineer. Full-stack developer. Physician. Academic.
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USD 50/hr
Doctorate
France

AI engineer. Full-stack developer. Physician. Academic.

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USD 50/hr
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Dr. Mark P.

Data science, machine learning, medical imaging, physicist. 15+yrs clinical research. Medical device development.
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USD 150/hr
PhD cum laude. Medical Physics
Netherlands

PhD, postdoc, senior researcher in medical physics, imaging, radiotherapy. Extraction of attributes from real-world collected data. Medical Im...

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USD 150/hr
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Sven A.

Bio-Research Engineer, MSc Clinical Research & Translational Medicine, RN, MSc Biostatistics
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USD 150/hr
MSc
United States

26 years experience in Research & Development of Medical Devices, Biotechnology, many years in basic science at KI, Charite, Cambridge, Oxf...

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USD 150/hr
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Dr. Ana Luiza C.

Freelance Medical writer, Clinical specialist and Regulatory affairs of Medical Devices, Ph.D. Biological Sciences
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USD 69/hr
MBA Quality Management
Brazil

I have over 8 years of experience in Clinical Research, Regulatory Affairs and Quality Assurance of implantable and electro medical devices in ...

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USD 69/hr
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Sonali S.

Experience in EUMDR, 510k submission, Risk management file, ISO 13485
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USD 20/hr
Bachelor of Pharmacy (Gold Medallist)
India

Having experience in medical device regulatory affairs, EUMDR, USFDA 510K, ISO 14971, ISO 13485

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USD 20/hr
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Beliz A.

Freelance Medical Writer, Medical Device Expert, 6+ years of Experience in Medical Device Industry
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USD 100/hr
M.S Neuroscience
Turkey

Bioengineer passionate about medical devices but even more loves to build meaningful, evidence-based relationships between medical devices and ...

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USD 100/hr
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Bina P.

Medical science liaison, medical writer, medical consultant with 5+ years of experience in clinical research.
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USD 60/hr
MD
United States

Strong medical professional with experience in medical writing, clinical research, pharmaceutical drug research and article writing. Ability to...

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USD 60/hr
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Damla V.

QA RA Consultant - Medical Device and Pharmaceutical Industry
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USD 50/hr
MS Horticulture and Agronomy
Turkey

Hi, I have almost 15 years of experience in a multinational Pharmaceutical and Medical Device company as a QA/RA manager. My Specialties -Exp...

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USD 50/hr
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Mariem R.

Study Start Up Specialist France | Sr CRA Medical | PMCF
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USD 100/hr
Master of Public Health
France

I have 15 years of experience in the field of Public Health and Clinical Research in several positions: coordination, monitoring, project man...

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USD 100/hr
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Kunle A.

Food scientist with 7 years of experience in regulatory consultancy, Technical Writer in SOP, Contract manufacturi
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USD 50/hr
BSc in Food Technology
Nigeria

I am a food scientist with 7years of experience. I have BSc in Food Technology and member Institute of Public Analyst of Nigeria (MIPAN). My e...

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USD 50/hr
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Find European Medical Device Regulation (MDR) Experts for hire on Kolabtree. Get consulting services from experienced specialists. Hire an EU MDR consultant today.

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