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

Dr. Ankur P.

Experienced CER Writer
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USD 85/hr
Master of Science
United States

My expertise is development of clinical evaluation reports (CERs). This includes experience with literature searches, post-market surveillance,...

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USD 85/hr
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Dr. Paolo S.

Medical Devices R&D | Validation and Verification following Q/RA | Computational simulation applied to MD
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USD 50/hr
PhD Engineering
United Kingdom

Doctor in Engineering specialised in medical devices research and development. Focused on validation and verification of development processes ...

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USD 50/hr
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Dr. Ralf H.

Independent medical device innovation consultant, RA/QA & projectmanagement of medical device developments
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USD 70/hr
PhD, polymer chemistry, degradable medical polyurethane
Netherlands

- I am a passionate and creative innovator with an entrepreneurial character and with a good feeling for quality. - I combine organizational kn...

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USD 70/hr
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Dr. Juliana D.

China Regulatory Consultant for Medical Device
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USD 120/hr
Bachelor's degree
Hong Kong

Team manager for RA and Quality, Regulatory Affairs: CFDA Registration experiences in Medical device field,(imported Class 3 MD includes Defibr...

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USD 120/hr
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Dr. Amin Y.

Head Of Regulatory Affairs at TUMS Preclinical Core Facillity
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Doctor of Pharmacy - PharmD
Iran, Islamic Republic of

Experienced Head Of Regulatory Affairs with a Demonstrated History of Working in the Biotechnology Industry. Skilled in Content Development, Tr...

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Dr. Paula P.

Medical Writer with 15+ years of experience in scientific writing
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USD 75/hr
PhD in Pharmaceutical Sciences
Portugal

- Degree in Pharmaceutical Sciences, Faculty of Pharmacy, University of Porto (2000) - PhD in Analytical Chemistry, Faculty of Pharmacy, Univer...

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USD 75/hr
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Dr. Bogdan M.

Global Regulatory Affairs in Medical Device industry
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USD 75/hr
Doctorate
Romania

I am an PhD Chemical engineer with proven experience in quality assurance and regulatory affairs. Currently I am the J. Manager Global Regulato...

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USD 75/hr
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Dr. Nadeem A.

Cell and Molecular Biologist | MBA in Medical devices and Healthcare Management | Certified in Regulatory Affairs - GxP
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USD 80/hr
The London School of Economics and Political Science (LSE)
Germany

• Cell biologist with seven years of academic scientific writing experience • MBA candidate in Medical Devices and Healthcare Management with t...

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USD 80/hr
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Dr. Eric L.

Regulatory Affairs & Quality Assurance Consultant (Medical Devices)
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USD 90/hr
Ph.D. Molecular Biology
Spain

With a strong scientific background, I bring extensive expertise in medical device development's regulatory and quality aspects. As an acco...

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USD 90/hr
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Dr. Evita A.

Medical Writer/Regulatory Affairs/Project Manager
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USD 210/hr
Masters degree in Biomedical Science
United States

A clinical research scientific writer with clinical medical, CSR. and regulatory CER expertise in MEDDEV 2.7/1 rev4 documentation, EU MDR and F...

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USD 210/hr
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Dr. Afsana S.

Enthusiastic medical writer with 3.5 years of experience in medical devices and drugs
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USD 10/hr
PharmD (Doctor of Pharmacy)
India

I'm Dr. Afsana Syed, Pharm.D having an overall experience of 3.5 years in Clinical Pharmacy (1 year) and medical writing (2.5 years). I'...

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USD 10/hr
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Dr. Derek C.

Freelance Scientific Editor | Experienced with Medical Devices, Pharmaceuticals, & in vitro Diagnostics
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USD 40/hr
Doctor of Philosophy (Ph.D)
Canada

I completed my PhD in Chemical Biology and have previously worked in the medical device, pharmaceutical, and in vitro diagnostics industries.

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USD 40/hr
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Dr. Sonia C.

Research and development, product development, program management, ISO 13485:2016, Medical Devices, In-vitro diagnostic
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USD 120/hr
PhD Microbiology
France

I have been working for the health industry, In-vitro diagnostic and medical devices for over 20 years, mainly at R&D positions and alw...

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USD 120/hr
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Dr. Anna T.

Process and project developer ● Design Thinking ● Healthcare
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USD 150/hr
PhD in Biomedical Sciences
Switzerland

Biomedical engineer with 4+ years of experience in collaborative research (medical...imaging for nuclear medicine applications) and several years of strategic management of scientific publications...

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USD 150/hr
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Dr. Harsh V.

Medical/Scientific/Regulatory/Newsletter/CMC/Dossier/Research/Review/Thesis/Protocol/Report/Article writing & editin...
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USD 30/hr
PhD
India

A competent pharma professional with experience in Scientific writing, Regulatory competitive intelligence, DRA, F&D, MSAT and QA. Experie...

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USD 30/hr
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Denise A.

Medical Device Global Quality and Regulatory Expert
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Bachelor's of Science and Associates of Business Administration
United States

I am an experienced Quality and Regulatory professional with over 25 years in the medical device manufacturing industry. I have worked with Cla...

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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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Juan Manuel F.

Clinical Project Manager, Research and Develop. Technical Expert and University Lecturer. 9+ years in clinical research
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USD 25/hr
Master in Project Management
Spain

Clinical Project Manager, Research and Development Technical Expert and University Lecturer. 9+ years in clinical research Studies: I have a b...

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USD 25/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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Balaji C.

Expert in EU MDR and EU MDD Remediation and Gap assessments. Good in Clinical evaluation plan and CER creation
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USD 10/hr
B.E. Mechanical engineering
India

MDR and MDD Gap assessments and Remediation. Risk documents creation and all remediation process knowledge to get the CE mark for the product t...

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USD 10/hr
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NAVEEN A.

Pharmaceutical & Medical device professional
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USD 50/hr
Masters in Biotechnology
India

Bio-pharma & Medical Device Quality Consultant having a good blend of Manufacturing, Technology & Business with in-dept...

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USD 50/hr
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AITZAZ r.

Oxford Alumnus, Biomedical Scientist, Futurist
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USD 70/hr
M.Sc (Master of Science)
Pakistan

Always, Keen On, Keep Walking, Born to Win!

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USD 70/hr
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Madhu S.

Experienced CER writer
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USD 75/hr
MBA
India

• A competent Professional Medical Writer with over 7+ years' of experience in Regulatory Compliance, Quality Systems, Clinical Research, ...

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USD 75/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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