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. Hrishikesh G.

Over 30 years of experience commercializing medical devices for large, mid-size and early stage companies.
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USD 125/hr
PhD in Electrical Engineering
United States

Broad hands-on software and hardware development for medical devices such as diagnostic imaging devices (PET, MRI, X-Ray and Ultrasound), blood...

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USD 125/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. 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. Vera M.

Clinical Research - Drug & Medical Device development and regulatory compliance (GCP/GLP/ISO 13485) - Expert Consult...
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USD 200/hr
Post-Doc
United States

Providing leadership and strategic direction in Drug/Medical Device Development and Quality assurance to meet the new Industry challenges Leade...

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USD 200/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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Sundeep A.

Medical Device, IVD, QMS, CE Certificate, FDA 510(K), EU MDR, MDSAP, ISO 13485, SaMD, PMS, CER , PMCF, Risk Management
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USD 100/hr
Master of Technology - Quality Management
India

A seasoned professional with a decade of experience, I am a Leader and Speaker in the field of Quality Assurance & Regulatory Affairs, ...

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USD 100/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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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. Hafsa I.

Medical Device Regulation (MDR) - BER - Technical File - CER - ISO13485 - Production manager - SOPs - Design File - GRIN
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USD 35/hr
PhD Biomedical Sciences
Pakistan

Medical Device Production Manager with 5 years of experience in device development - Technical file - Design File - Procurement - Technology De...

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USD 35/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. Jean J.

Freelance Senior Ultrasound Physicist, Data Scientist, Software and web developer
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USD 250/hr
PhD - Physics
France

I am a highly experienced ultrasound engineer with a PhD in Physics/Ultrasound Imaging. I have over 10 years of experience in the ultraso...

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USD 250/hr
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Dr. Sharma P.

Highly skilled QA and RA certified lead auditor with diverse industry experience in more than 56 markets with UK's N...
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USD 40/hr
M.Sc. (by Research) Biomedical Sciences
United Kingdom

Implementing ISO13485 and ISO9001 quality systems for various market requirements building compliant and conformant QMS and product regulatory ...

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USD 40/hr
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Mark L.

Digital Health Consultant, Medical Doctor, Biomedical Engineer, Certified PMP, Lean Six Sigma Black Belt, 12 yrs med dev
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MD
United States

Mark Luhovy, MD is a medical doctor and biomedical engineer who has dedicated 20 years to the pursuit of understanding the intersection of medi...

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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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Mike K.

FDA Regulatory Consultant
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USD 150/hr
Bachelor of chemistry and Biochemistry
United States

Mr. Khalil’s professional career spans over thirty (30) years of executive and entrepreneurial leadership in pharmaceutical, medical devices, n...

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USD 150/hr
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Krishnakant S.

Regulatory Toxicologist | Specializing in Toxicological Hazard Assessment, Risk Evaluation, and Regulatory Compliance
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USD 25/hr
Masters in Pharmacy (Pharmacology)
India

Regulatory Affairs and Toxicology Expertise: 1. Proficient in toxicological hazard assessment and human risk evaluation for product safety acro...

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USD 25/hr
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Obuchinezia A.

Expert Medical Affairs Professional | Medical Communications | Project Conceptualisation | RWD/RWE | eCOA
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USD 65/hr
MSc Drug Discovery and Development
United Kingdom

A dynamic and results-driven Medical Affairs Professional with extensive experience in conceptualising, developing, and managing international ...

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USD 65/hr
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Minh Tuan T.

High-achieving individual with 4+ years in medical device regulations (EUMDR & FDA) and business process development...
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USD 85/hr
Masters of Science
United States

Regulatory and Clinical Affairs Maintained strong customer relations, providing exceptional on-site technical, clinical, and sales support to o...

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USD 85/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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Johannes e g Hans V.

Global Expert in Quality engineering management, Auditing, and Regulatory Compliance, SQE. Delivering results for proces
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USD 125/hr
BSc Engineering
Netherlands

Eager to contribute with my passion for quality improvement, attention to detail, and auditing expertise, ensuring success process architecture...

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USD 125/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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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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