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

Dr. Kurtulus G.

Expert with 10+ Years of Experience in Medical, Scientific and Technical Writing
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USD 150/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 150/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 Ph.D. in pharmaceutical science. My writing qualifications: - Writing in the Sciences Certificate (Stanford Univers...

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USD 50/hr
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Dr. Kenneth F.

Scientist with 5+ years of experience in clinical research, molecular assay design & development. SAS-certif...
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USD 120/hr
PhD Biomedical Engineering
Canada

• Advanced understanding of molecular diagnostics, biotechnology, and biomedical engineering concepts, with strong organizational, leadership a...

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USD 120/hr
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Dr. Muhammad M.

Being Molecular biologist, my profession, not only profession but my passion is to technically write scientific stuff.
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USD 100/hr
PhD
Pakistan

"Hello and welcome to my freelance profile! I am a scientific writer and product development specialist with several years of experience ...

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USD 100/hr
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Dr. Diksha V.

Scientist & Writer | Expert in life science, cancer biology, drug discovery | Data science/analysis & bioinforma...
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USD 50/hr
PhD
India

I am a doctorate in life sciences with an experience of over 9 years in the academic and corporate sector. I have managed projects focusing on...

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USD 50/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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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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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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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. 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. 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. 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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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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Tasmiatul K.

B. Pharm, M. Pharm, PGDIM, MBA (DU), QA and Regulatory Specialist of Medicinal Products
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USD 90/hr
Masters of Business Administration (MBA)
Australia

1. Registered and Licensed Pharmacist (RPh) in Bangladesh (Reg. No- A 4845) 2. Experienced Professional equipped with skills in the field of Re...

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USD 90/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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Ashwini L.

Quality Management System, Risk Assessment, Post Market Surveillance, Lead Auditor ISO 13485, Compliance Expert
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USD 70/hr
Bachelors
Netherlands

Over 15 years of experience in Quality and Regulatory Affairs, Risk Assessment, Verification, and Validation, of medical devices like Patient M...

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USD 70/hr
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Kalidoss P.

https://www.linkedin.com/in/kalidoss-p-09353a65
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USD 10/hr
Biomedical Engineering
India

Work experience in Medical device regulatory, cybersecurity of the medical device, clinical evaluation report analysis, risk benefit analysis.

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USD 10/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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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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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. 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. Danielle K. B.

Clinical Research Professional with Medical Writing experience | Medical Device | Pharmaceutical | Biotechnology
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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 ares including Respiratory, Cardiology, Men's H...

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USD 60/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. 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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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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