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

Dr. Ahram Q.

Expert Life Science's Researcher, writer, and Consultant
Create Project
★★★★★
☆☆☆☆☆
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...

★★★★★
☆☆☆☆☆
USD 50/hr
Contact3

Dr. Hrishikesh G.

Over 30 years of experience commercializing medical devices for large, mid-size and early stage companies.
Create Project
★★★★★
☆☆☆☆☆
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...

★★★★★
☆☆☆☆☆
USD 125/hr
Contact3

Dr. Kurtulus G.

Expert with 10+ Years of Experience in Medical, Scientific, Technical and Regulatory Writing
Create Project
★★★★★
☆☆☆☆☆
USD 100/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...

★★★★★
☆☆☆☆☆
USD 100/hr
Contact3

Dr. Nare S.

More than 10 years of experience as Regulatory Affairs Specialist, Medical and Scientific Writer, Clinical Trial Consult
Create Project
★★★★★
☆☆☆☆☆
USD 50/hr
PharmD (Doctor of Pharmacy)
Armenia

My science qualification is a Ph.D. in pharmaceutical science. My writing qualifications: - Writing in the Sciences Certificate (Stanford Unive...

★★★★★
☆☆☆☆☆
USD 50/hr
Contact3

Dr. Muhammad M.

Data-Driven Scientist Specializing in Comprehensive Data Analysis and Scientific Writing for Advanced Research Projects
Create Project
★★★★★
☆☆☆☆☆
USD 30/hr
PhD
Pakistan

Hello and welcome to my freelance profile! I am an accomplished Data-Driven Scientist with extensive expertise in comprehensive data analysis a...

★★★★★
☆☆☆☆☆
USD 30/hr
Contact3

Dr. Vera M.

Clinical Research - Drug & Medical Device development and regulatory compliance (GCP/GLP/ISO 13485) - Expert Consult...
Create Project
★★★★★
☆☆☆☆☆
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...

★★★★★
☆☆☆☆☆
USD 200/hr
Contact3

Nida A.

Experienced MDR and FDA certified CER/Technical File Writer with 7+ years of experience with multinational industries
Create Project
★★★★★
☆☆☆☆☆
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...

★★★★★
☆☆☆☆☆
USD 50/hr
Contact3

Madhu S.

Quality and Regulatory Affairs professional | Expert in CE marking, EU MDR 2017, FDA submissions & lead auditor ISO1...
Create Project
★★★★★
☆☆☆☆☆
USD 40/hr
Advanced PG Diploma in CR & Regulatory Affairs (APGDCR-RA)
India

Over 10 years’ experience in Quality and Regulatory Affairs, and technical submissions for a range of medical devices, including Orthopaedics, ...

★★★★★
☆☆☆☆☆
USD 40/hr
Contact3

Lisa R.

REGULATORY AFFAIRS - Medical Device - Biotech - Dietary Supplement - Pharma
Create Project
★★★★★
☆☆☆☆☆
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...

★★★★★
☆☆☆☆☆
USD 200/hr
Contact3

Sundeep A.

Medical Device, IVD, QMS, CE Certificate, FDA 510(K), EU MDR, MDSAP, ISO 13485, SaMD, PMS, CER , PMCF, Risk Management
Create Project
★★★★★
☆☆☆☆☆
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, ...

★★★★★
☆☆☆☆☆
USD 100/hr
Contact3

Adam F.

exFDA Investigator / expert in Medical Device & Combination Product design, manufacturing, and compliance
Create Project
★★★★★
☆☆☆☆☆
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...

★★★★★
☆☆☆☆☆
USD 200/hr
Contact3

Girish H.

Freelance Medical Writer / Regulatory Expert in Medical Device with 16+ Years of Experience (EUMDR, ISO 13485, FDA510K)
Create Project
★★★★★
☆☆☆☆☆
USD 90/hr
B.Pharmacy
India

An accomplished, versatile, results-oriented clinical research professional with over 16 years of experience in the Pharmaceuticals & M...

★★★★★
☆☆☆☆☆
USD 90/hr
Contact3

Rudra P.

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

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

★★★★★
☆☆☆☆☆
USD 70/hr
Contact3

Dr. Hafsa I.

Medical Device Regulation (MDR) - BER - Technical File - CER - ISO13485 - Production manager - SOPs - Design File - GRIN
Create Project
★★★★★
☆☆☆☆☆
USD 35/hr
PhD Biomedical Sciences
Pakistan

Medical Device Production Manager with 5 years of experience in device development - Technical file - Design File - Procurement - Technology De...

★★★★★
☆☆☆☆☆
USD 35/hr
Contact3

Dr. Pavel O.

AI engineer. Full-stack developer. Physician. Academic.
Create Project
★★★★★
☆☆☆☆☆
USD 50/hr
Doctorate
France

AI engineer. Full-stack developer. Physician. Academic.

★★★★★
☆☆☆☆☆
USD 50/hr
Contact3

Dr. Sharma P.

Highly skilled QA and RA certified lead auditor with diverse industry experience in more than 56 markets with UK's N...
Create Project
★★★★★
☆☆☆☆☆
USD 40/hr
M.Sc. (by Research) Biomedical Sciences
United Kingdom

Implementing ISO13485 and ISO9001 quality systems for various market requirements building compliant and conformant QMS and product regulatory ...

★★★★★
☆☆☆☆☆
USD 40/hr
Contact3

Dr. Paolo S.

Medical Devices R&D | Validation and Verification following Q/RA | Computational simulation applied to MD
Create Project
★★★★★
☆☆☆☆☆
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 ...

★★★★★
☆☆☆☆☆
USD 50/hr
Contact3

Mark L.

Digital Health Consultant, Medical Doctor, Biomedical Engineer, Certified PMP, Lean Six Sigma Black Belt, 12 yrs med dev
Create Project
★★★★★
☆☆☆☆☆
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...

★★★★★
☆☆☆☆☆
Contact3

Dr. Ana Luiza C.

Freelance Medical writer, Clinical specialist and Regulatory affairs of Medical Devices, Ph.D. Biological Sciences
Create Project
★★★★★
☆☆☆☆☆
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 ...

★★★★★
☆☆☆☆☆
USD 69/hr
Contact3

Krishnakant S.

Regulatory Toxicologist | Specializing in Toxicological Hazard Assessment, Risk Evaluation, and Regulatory Compliance
Create Project
★★★★★
☆☆☆☆☆
USD 25/hr
Masters in Pharmacy (Pharmacology)
India

Regulatory Affairs and Toxicology Expertise: 1. Proficient in toxicological hazard assessment and human risk evaluation for product safety acro...

★★★★★
☆☆☆☆☆
USD 25/hr
Contact3

Obuchinezia A.

Expert Medical Affairs Professional | Medical Communications | Project Conceptualisation | RWD/RWE | eCOA
Create Project
★★★★★
☆☆☆☆☆
USD 65/hr
MSc Drug Discovery and Development
United Kingdom

A dynamic and results-driven Medical Affairs Professional with extensive experience in conceptualising, developing, and managing international ...

★★★★★
☆☆☆☆☆
USD 65/hr
Contact3

Biomedical E.

MEDICAL DEVICE REGULATORY CONSULTANT EU-MDR | EU IVDR | SaMD | FDA | MHRA | SFDA | Germany | 7+ years’ Experience
Create Project
★★★★★
☆☆☆☆☆
USD 30/hr
MS Biomedical Engineering
Pakistan

I am Umair Ahmed, a seasoned Biomedical Engineer and Scientist offering over 7 years of comprehensive experience in the freelance medical devic...

★★★★★
☆☆☆☆☆
USD 30/hr
Contact3

Kunle A.

Food scientist with 7 years of experience in regulatory consultancy, Technical Writer in SOP, Contract manufacturi
Create Project
★★★★★
☆☆☆☆☆
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...

★★★★★
☆☆☆☆☆
USD 50/hr
Contact3

Dr. Sergio P.

MDR Consultant / CER writer
Create Project
★★★★★
☆☆☆☆☆
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 ...

★★★★★
☆☆☆☆☆
USD 55/hr
Contact3

Dr. SENTHILKUMAR S.

Helping Medical Device Companies as an SME in developing CEP, CER, PMS Plan, PSUR, PMCF Plan & Report and Manusc...
Create Project
★★★★★
☆☆☆☆☆
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...

★★★★★
☆☆☆☆☆
USD 75/hr
Contact3

Find European Medical Device Regulation (MDR) Experts for hire on Kolabtree. Get consulting services from experienced specialists. Hire an EU MDR consultant today.

pay-per-click
Confidentiality Assured

We take several measures to help you work with full confidence and peace of mind.

Keep your project private

Restrict who can see your project and send you proposals. Invite only specific freelancers to view your project.

NDAs and IP protection

Our T&C include a default confidentiality clause that protects your IP and NDA for added protection before disclosing project details.

Kolabtree ensures safety and security of your payments and personal information and project details. Kolabtree’s T&C includes a default confidentiality and NDA clause.

You will receive detailed proposals directly from Kolabtree. These proposals will include a comprehensive Statement of Work (SOW), project fees, milestones, and deadlines.

You can choose to pay either a fixed or an hourly fee based on your scope of work. Pre-pay for the next milestone. You have to approve the deliverables only if the quality meets your expectations. If you arn’t happy, we’ll refund your money.

Kolabtree will share multiple quotations for your project. You have the freedom to accept the quote that aligns with your project requirement and budget. You can get in touch with us in case you want to discuss the fee.

Our T&C include a default confidentiality clause that protects your IP and NDA for added protection.

Why Kolabtree

Contact experts directly

Speak directly with freelancers and explain your requirements.

100% satisfaction guaranteed

You have to approve the deliverables only if quality meets your expectations. If you arn’t happy, we’ll refund your money.

Project Management

Keep track of files and conversations in the user-friendly Workspace.

Flexible, secure payments

You can choose to pay either a fixed or an hourly fee based on your requirement.

Recent Projects
  • EU MDR consulting services needed
    $550.00
How it works View full page
1

Post your Project (Free)

Your project details are safe, secure and visible only to logged-in users.

2

Get Quotes & Choose Experts

Discuss your requirements in detail with the experts before accepting the final statement of work from Kolabtree.

3

Collaborate

Pre-pay for your project and work with the expert to get your desired output. Keep track of files and conversations in the user-friendly Workspace.

4

Job Done!

Approve the deliverables once you're satisfied with the job done.