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

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. 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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Dr. SENTHILKUMAR S.

Helping Medical Device Companies as an SME in developing CEP, CER, PMS Plan, PSUR, PMCF Plan & Report and Manusc...
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USD 75/hr
Ph.D
India

Scientific Writer with 10+ years of experience with a demonstrated history of working in the Medical Device domain, SME in Clinical Evaluations...

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USD 75/hr
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Dr. Dilip B.

Endorsed by the Royal Academy of Engineering as having exceptional Talent in Biomedical and Medical sciences
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USD 150/hr
PhD, Neuroscience
United Kingdom

I am the holder of highly prestigious Tier 1 Exceptional Talent Visa and endorsed as such by the Royal Academy of Engineering in the fields of ...

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USD 150/hr
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Dr. Muhammad H.

Freelance Molecular biologist and Bioinformatician. I have 5+ years of experience in technical scientific writing.
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USD 50/hr
Doctor of Philosophy
Pakistan

It's me Dr.Hamdan, professionally computational biologist. My profession, not only professionally, but my passion is to interact with globa...

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USD 50/hr
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David P.

Medical Device Commercialization and Manufacturing Automation Consultant in a Regulated Environment
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USD 170/hr
Mechanical Engineering
United States

I am a process and product development commercialization consultant and project manager with an automation and mechanical engineering backgroun...

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USD 170/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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Yordan P.

Medical Device Consultant for NA and EU markets. Experience in market research, clinical research, and grant writing.
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USD 80/hr
Master of Translational Medicine
United States

I am a medical student (UF) with a masters in medical innovation (UC Berkeley and UCSF). I have been working part-time as a medical product con...

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USD 80/hr
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Rudra P.

Group of Clinical Research Professionals (Project Manager, Biostatisticians, CRAs, Medical Writers, SAS Prgmers)
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USD 70/hr
MS
India

We are a Contract Research Organization (CRO) that focuses on advanced project management, clinical operations, medical writing, statistical an...

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USD 70/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
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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Bharti S.

Scientific & Medical writer, COVID-19 virologist, Journal manuscript writing, Editor, Research papers, clinical tria...
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USD 102/hr
Master of Public Health (M.P.H.), Fundamentals of Clinical Trials
India

A strong background in virology, medical microbiology and public health qualifies me to work on COVID-19 projects (factsheets, COVID-19 at home...

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USD 102/hr
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Dr. Arinzechukwu U.

Freelance Scientific Writer and Consultant with over 6+ years in cancer research
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USD 100/hr
Molecular Haematology
United Kingdom

I have over 10+ years experience in medical/content/copywriting and proof-reading/editing as well as over 6+ years experience in cancer researc...

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USD 100/hr
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Dr. Sathesh Kumar A.

Regulatory Affairs Specialist
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USD 50/hr
Ph.D
India

Fourteen years of R&D, Regulatory and Medical writing experience in various disciplines across In-vitro diagnostics, medical device regulat...

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USD 50/hr
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Dr. Grace C.

Experienced CER Writer for medical device companies
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USD 50/hr
Doctor of Philosophy (PhD) in Molecular Medicine
Malaysia

1. Clinical Evaluation Report (CER) writer and authoring of Clinical Evaluation Plan (CEP) in accordance with Medical Device Regulation (MDR), ...

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USD 50/hr
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Dr. Sandeep P.

Ph.D. in Chemistry with 14 years of experience in regulatory affairs of pharmaceutical products and medical devices
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USD 30/hr
PhD (Chemistry)
India

Ph.D. in Chemistry having a total of 14+ years of experience in the pharmaceutical industry, expertise in the regulatory intelligence of pharma...

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USD 30/hr
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Dr. Imen F.

Freelance: Quality Assurance/ Regulatory Affairs specialist in Medical Devices (MD)
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USD 150/hr
Quality Expert
France

PHD pharmacist, with more than 5 years of experience in Quality Assurance (QA) and Regulatory Affairs (RA). My experience enables me to help yo...

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USD 150/hr
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Dr. Trinadh Venkata Satish T.

Experienced research scientist keenly interested in contributing to medical devices, health care and biotech projects.
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USD 50/hr
Postdoctoral Research (Department of Molecular Cellular and Developmental Biology)
Netherlands

Experienced Research Scientist with a Ph.D. and over 20+ years of demonstrated history of working in the areas of Tissue Engineering, Infectiou...

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USD 50/hr
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Dr. Waqar L.

Auditing, Consulting, Training and Operations Management for International Standards i.e. ISO, BSCI, DIN, MDD, MDR, PPE
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USD 75/hr
PhD
Pakistan

Ten + years of hands-on technical working experience in the manufacturing environment covering Metal, Textiles, Food, Auto parts, Chemical proc...

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USD 75/hr
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Dr. Sarah C.

Consultant in Digital Health & Life Sciences | Chemist | Expert in Digital Health, Drug Discovery & Organic Che...
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USD 50/hr
PhD (Chemistry)
Indonesia

Consultant to the digital health & life sciences industry with a strong research background in early stage drug discovery. I have extensive...

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USD 50/hr
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Dr. Azza G.

Medical Regulatory Writer and Editor, Clinical Evaluation Specialist
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USD 25/hr
PhD
Germany

Ph.D. trained clinician with expertise in bone biology, inflammation, and osseointegration. Established a career as a medical writer three year...

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USD 25/hr
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Dr. Nitin M.

Scientific Advisor at Melior Life Sciences (CRO) | Consultant Radiologist | AI Research Advisor at Synapsica |
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USD 125/hr
MD
India

After completing MBBS from the All India Institute of Medical Sciences, New Delhi. He pursued MD in Radiodiagnosis from SMS Medical College and...

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USD 125/hr
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Dr. Codette P.

One stop solution for end to end Life Sciences global Regulatory support.
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USD 50/hr
PhD
India

Codette Pharma Regulatory Analytics Pvt Ltd provides top-level global regulatory and clinical support to Life Science companies. We are experts...

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USD 50/hr
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Dr. Krutika G.

CMedO| Medical Device Expert | 10+ years of experience in healthcare with clinical and usability research
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USD 200/hr
PhD Neurophysiology (Emphasis Psychology)
Germany

Here you can find more info:https://www.krutikagohil.com/ I am an award-winning professional digital health innovator. With my well-founded s...

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USD 200/hr
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Dr. Imen S.

Quality mangement/Audit
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USD 50/hr
Training in Quality, Safety and Environmental Management
France

monitoring and advising on the performance of the quality management system, producing data and reporting on performance, measuring against set...

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USD 50/hr
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Dr. Alpa B.

Medical writer with 8+ years of experience in writing CEPs, CERs, PMSRs and SSCP for Class II Medical Devices
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USD 30/hr
Bachelor of Dental Surgery
India

I am Dr. Alpa Ben, a BDS graduate from India. I have been working with healthcare service industry from past 8 years and have experience in var...

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USD 30/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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