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

Haralabos P.

Medical/Pharma English into Greek translator with medical background (MD, MSc, PhD, Certified Radiologist)
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USD 35/hr
Certificate in Translation
Greece

Working as a medical translator for the past 19 years (9 years full time), I have translated a wide range of biomedical documents including med...

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USD 35/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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Dr. Sunday Ojochegbe O.

R and D Scientist in Medical device industry | Cancer research | Process Validation | Project Management and Nonprofit...
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USD 30/hr
MBA
Luxembourg

Dr. Okutachi is an experienced R and D Scientist in the highly regulated molecular diagnostics | IVD industry. He holds a PhD in Cancer Cell B...

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USD 30/hr
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Dr. Ioannis L.

Pharmaceutical Industry professional with 5+ years of experience in drug development
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USD 160/hr
PhD Biopharmaceutics & Pharmacokinetics
Switzerland

Accomplished pharmaceutical industry professional with strong background in clinical pharmacology and translational medicine. Experienced in he...

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USD 160/hr
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Dr. Rafaella P.

10 years of progressive experience in the field of biotechnology research, scientific writing, and mentoring.
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USD 50/hr
Chemistry PhD
Brazil

A research engineer with progressive experience across nanomaterials, hybrid materials, polymers, and composites, with knowledge in additive ma...

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USD 50/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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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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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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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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Usman M.

Medical Devices Consultant | Compliance, Quality, and Risk Management, Regulatory Affairs
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USD 50/hr
Masters in Biomedical Engineering
Germany

Career Profile Regulatory Affairs Specialist with 5+ years of experience, in the creation and compilation of regulatory submissions to regulato...

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USD 50/hr
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Dr Febin F.

Scientific Writer with 3+ year experience
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USD 50/hr
Doctor of Pharmacy
India

• Scientific Writer with experience in end-to-end handling of Clinical Evaluation Reports (CERs, both MDD and MDR compliance). • Authored scien...

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USD 50/hr
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Michal H.

Regulatory Affairs, EMEA - MDD/MDR, IVDD/IVDR; Quality Assurance - Manufacturer/Distributor, Lead Auditor ISO9001:2015
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Masters (Science)
Austria

Regulatory notifications under IVDD - Czech republic, Slovakia Regulatory notifications under MDD - Central Eastern Europe Regulatory registrat...

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Lini S.

Regulatory Affairs Expert with 20 Years Experience (Regulatory and Scientific Writing Services)
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USD 90/hr
MSc Pharmaceutical Chemistry
India

Specialities - Well-versed in EU Registration procedures (DC/MR, CP and nationals). - CMC Dossier Development & writing - Regulatory St...

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USD 90/hr
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Thelma A.

Pharmacist | Pharmaceutical & Medical research and writing
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USD 30/hr
MSc Industrial Pharmaceutics
Canada

A pharmacist with over 6years of experience in the healthcare, medical device and pharmaceutical industry. Invested in carrying out research a...

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USD 30/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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Surya N.

CMC Expert with 20+ years of Regulatory and Formulation experience for USFDA, EMEA, Japan, Canada and ROW Markets
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USD 90/hr
M.Pharm.
India

SME (Subject Master Expert) in the Regulatory Affairs and Compliance Development of Finished Formulations (OSD and Injectable) Scientific Advi...

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USD 90/hr
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Mahesh varma N.

Physician with medical communication and consulting experience
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USD 54/hr
MIHMEP
India

Medical writing, Regulatory Writing, CER writing, Scientific consulting, Design, Biostatistics

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USD 54/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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Ramamurthy J.

End-to-End writing and project life cycle management of CEP/CER, PMSP/PMSR/PSUR, PMCFP/PMCFER and SSCP
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USD 100/hr
M.Sc Biochemistry
India

▪ Writing, reviewing quality and ensuring timely delivery of CEP/CER, PMSP/PMSR/PSUR to the client according to EU-MDR/MDD regulations and rela...

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USD 100/hr
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Ben C.

Therapeutic Goods Consultant: Quality Systems, Regulatory Affairs, Auditing, Product Development and Validations
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USD 150/hr
Diploma in Quality Auditing
Australia

I'm a therapeutic goods industry professional, working within the Australian medical device and pharmaceutical manufacturing sectors since ...

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USD 150/hr
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Ilkay K.

EU MDR Specialist with years of QMS experience working with companies like Tüv and Dekra as Lead Auditor
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USD 50/hr
Master of Communication in Digital Media
Germany

20+ years of QMS experience, ISO 9001 Lead Auditor, ISO 14001, ISO 13485. Heading currently a team of MDR consultant in Germany and providing M...

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USD 50/hr
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Soundarya P.

Scientific writer with 3+ years of hands-on experience in developing and reviewing clinical evaluation reports-MDD&M...
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USD 45/hr
Masters of Pharmacy
India

Handled more than 30 clinical evaluation reports end to end, starting from clinical evaluation plan, literature screening, literature summaries...

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USD 45/hr
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Caique M.

- Post-market surveillance Analyst - Medical writer with experience in CER and PMS.
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USD 80/hr
Bachelor in Biomedicine
Brazil

I am a freelance science and medicine writer, my focus is on implantable medical devices related to the areas of orthopedics. I specialized in ...

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USD 80/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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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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Alexander B.

Early Phase Oncology, Expert in Trial Management, Client Relations, Site Relations, 12 years experience
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USD 250/hr
BS - Molecular Biology
United States

I have 12 years experience, starting as a Lead Coordinator at a clinical research site. Worked in the CRO space in study start-up, as a CRA, Cl...

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USD 250/hr
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Selina B.

Experienced medical writer
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USD 70/hr
Doctorate of Medicine (MD)
United States

Medical Communications Consultant -Writing Clinical Evaluation Reports (CER) for medical device manufacturers -Preparation of clinical reports ...

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USD 70/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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