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

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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Pradip F.

R & D Expert, Scientific Advisor/Strategist/consultant with >20 years of experience in Lifesciences and Healthcar...
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USD 30/hr
M.Sc.
India

I am managing R & D project for in-vitro diagnostics, in-vitro drug screening, medical device, and vaccine development. I look into all as...

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USD 30/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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Kavita S.

Experienced Medical Device Regulatory Affairs professional
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USD 40/hr
Post Graduate Diploma in Management (PGDM)
India

We are a team of experienced regulatory compliance expertise for Medical Devices and In-Vitro diagnostic devices across all risk classes. We ha...

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USD 40/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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Damla V.

QA RA Consultant - Medical Device and Pharmaceutical Industry
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USD 50/hr
MS Horticulture and Agronomy
Turkey

Hi, I have almost 15 years of experience in a multinational Pharmaceutical and Medical Device company as a QA/RA manager. My Specialties -Exp...

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USD 50/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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Lakshman Prakash B.

experience in Lifesciences in QA, QMS, Regulatory, EU-IVDR, medical device documentation writing clinical trial reports
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USD 100/hr
M.Sc Biochemistry
India

Experience in Lifesciences industry including over 18 years’ experience in QA, QMS, Regulatory, Manufacturing, Quality Unit (Commissioning, Qua...

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USD 100/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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Jacqueline V.

Clinical researcher (MICR) and Medical writer skilled in Clinical Evaluations MDR IVDR, PMS(PMSR/ PSUR) and PMCF plans
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USD 120/hr
Clinical Evalutions for MDR and IVDR
United Kingdom

Registered healthcare professional with 16 years of clinical experience in academic hospitals and clinical research. Trained in Clinical Evalua...

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USD 120/hr
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Akhthar S.

Management Consultant maximizing clients profits through VALUE SELLING
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USD 285/hr
MBA
United States

Sr. Executive & Entrepreneur with experience in Biotech, SaaS Healthcare, Medical Devices, Biomaterials- Cellulose, fibers, starch, PHA, PB...

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USD 285/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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Tarun P.

Regulatory Expert (Consultant) having 25 years of experience working with Pharma, CRO and Medical Device Industry
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USD 150/hr
MBA
India

Vision-driven executive with over 25 years of demonstrated leadership in the pharmaceuticals industry. Proven track record of driving bold init...

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USD 150/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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Jose A.

Freelance Medical Device professional with over 25 years of experience implementing QMS systems and RA compliance
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USD 175/hr
M.S Clinical Nutrition
United States

Behind every successful medical device registration, there is a team of experts working hard to ensure it meets regulatory requirements. As a Q...

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USD 175/hr
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Sarah B.

Biostatistics consulting services & data analysis by industry experienced Biostatistician (Medical Statistician)
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USD 130/hr
Masters of Biostatistics
United Kingdom

I'm a qualified Biostatistician with several years experience in the design and analysis of clinical studies including clinical trials. Thi...

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USD 130/hr
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Arjun L.

Physician | Clinical & Medical Affairs | CER | Scientific Writing | Pharma labeling | Strategy | HealthTech ...
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USD 70/hr
Masters of Public Health (Epidemiology, Clinical Infectious Diseases and Global Health Majors)
India

I have a blend of experience in clinical medicine, pharmaceutical industry and medical device industry....As a medical doctor, I work on infectious diseases, pulmonary and critical care and public health....

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USD 70/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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Peter O.

Experienced quality assurance and regulatory affairs professional in the medical device industry.
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USD 300/hr
MS Engineering Management
United States

Product experience includes Class 1, 2 and 3 devices: external defibrillators, AEDs, infusion pumps, patient monitors, image guidance, ventilat...

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USD 300/hr
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Viktoria K.

Idependent Clinical Study Protocol Reviewer and Specialist with 14 years in depth experience in clinical research| Coach
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USD 200/hr
Environmental Enineering - M.Sc
Ireland

I am an independent clinical research professional with 14 years experiences in the sector. My expert area is clinical trial protocol content r...

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USD 200/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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Tamil S.

5 years experience as an Quality Assurance professional.
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USD 60/hr
Bachelors of Engineering
India

5 years experience as an Quality Assurance professional.I have a broad background, topics include: - ISO 13485:2016 - 21 CFR 820 - ISO 14971, ...

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USD 60/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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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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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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