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Top Freelance EU In vitro Diagnostic Regulation (IVDR) Compliance Experts for Hire

Karissa T.

Your Partner in Regulatory Success | 17+ Yrs | 510(k), EU MDR, IVDR | Expert Support Within Your Budget
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USD 150/hr
Masters Regulatory Science
United States

I’m a seasoned Regulatory Affairs Consultant with over 17 years of experience supporting medical device and IVD companies in achieving global c...

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USD 150/hr
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Dr. Harriet K.

Regulatory Toxicologist
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USD 495/hr
PhD
United States

Regulatory writing and submissions • Regulatory Intelligence and Strategy Development • Toxicology Study Monitoring • Due Diligence and Gap Ana...

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USD 495/hr
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Dr. Jan S.

Scientfic Expert | Critical Reader and Writer | PK/PD Specialist | Experiment and Product Designer | Regulatory Affairs
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USD 60/hr
Doctor of Philosophy - PhD
Austria

🚀 Your Go-To Scientific Consultant for Mission-Critical Projects 🚀 Need an expert who can not only understand complex science ...

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USD 60/hr
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Dr. Anushikha D.

Dentist and and MPH with 6+ years in evidence-based medical and scientific writing, research, and medical communication
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USD 42/hr
Master of Public Health
India

I am a dentist and public health professional with a Master's in Public Health from All India Institute of Medical Sciences (AIIMS), Rishik...

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USD 42/hr
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Edwin M.

Health, Medical & Wellness Content Writer
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USD 15/hr
Business Information Technology
Kenya

As a content writer, I craft compelling content that not only engages readers but also drives traffic. With a keen eye for detail and a deep un...

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USD 15/hr
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ALOKEPARNA C.

Medical Device Regulatory Affairs Consultant | QMS, DHF, EU MDR, ISO 13485
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USD 60/hr
Healthcare Management
India

I help medical device startups, diagnostic innovators, and digital health companies build robust and compliant documentation aligned with ISO 1...

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USD 60/hr
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Dr. Ziaullah Z.

Freelance Regulatory Affairs Specialist for Drugs, and Medical Devices/Regulatory Writer, Drug Developer
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USD 100/hr
Master in Regulatory Affairs for Drugs, Biologics and Medical Devices
United States

Bridging the gap between complex chemical problem-solving and strategic regulatory navigation, I contribute to the development of innovative ph...

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USD 100/hr
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Dr. Vinay V.

Research Scientist in Biosensors & Translational Diagnostics | Nanobiotechnology & Biomarker Detection Expert
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USD 100/hr
PhD (Medicine)
India

I am a Research Scientist specializing in Biosensors and Translational Diagnostics, with over ten years of experience across academia, clinical...

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USD 100/hr
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Dr. Ts. Muhamad Afiq Faisal Y.

Business Development | Researcher (Pharmacology, Infectious & Neurodegenerative Diseases) | Lecturer | Marketer
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USD 20/hr
Doctor of Philosophy (Ph.D)
Malaysia

I am a results-oriented professional with a PhD in Pharmacology and Toxicology, complemented by industry experience in international business d...

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USD 20/hr
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Dr. Sotirios B.

Molecular Biology | Translational Research | Scientific Editing | Research Integrity. 20+ years of research experience
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USD 30/hr
PhD in Molecular Biology
Greece

Experienced scientific editor with a passion for helping fellow researchers share their innovative work with the world. With >6 years of exp...

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USD 30/hr
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Eddie W.

10 year ex-Abbott RA/QA professional | Expert in ISO 13485, CE Marking, 510(k) and WHO PQ for MD and IVDs
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USD 165/hr
Masters in Public Health
Switzerland

I'm excited to help businesses reach market approval on their new or existing medical devices and IVDs. I have experience working with both...

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USD 165/hr
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Raksha R.

Biotech Strategist with 3+ years in pharma | Competitive Intelligence, KOL Mapping & APAC Regulatory
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USD 400/hr
Master's degree (Research), Biomedical Sciences: Infection and Immunity
Sweden

I am a biotech strategy consultant specializing in competitive intelligence, regulatory pathways, and market access strategy for rare disease t...

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USD 400/hr
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Bruce T.

Biomedical engineering graduate with 3.5+ years expertise in medical device development & quality/regulatory complia...
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USD 30/hr
Master of Engineering
Canada

I have a Bachelor's in Biomedical Engineering from Toronto Metropolitan University (formerly Ryerson) and a Master's of Biomedical Engi...

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USD 30/hr
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Joana O.

AR Surgical Deployment & Medical Device Validation Specialist | MSc Medical Imaging | HIPAA & GDPR Certified
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USD 20/hr
Master of Science Medical Imaging and Applications
France

Biomedical engineer and clinical deployment specialist with hands-on experience integrating AR-guided surgical systems into live operating room...

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USD 20/hr
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Dr. Mehdi F.

MEDICAL & SCIENTIFIC AFFAIRS CONSULTANT -R&D MD, msc
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USD 100/hr
Masters of Science
France

Scientific and regulatory consulting for MedTech, pharmaceutical, IVD, and AI-driven diagnostics companies. Physician-scientist (MD, MSc Bioin...

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USD 100/hr
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Ojas K.

End-to-end IVD consultant specializing in ISO 13485, CE-IVDR compliance, QMS, and diagnostic product development
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USD 40/hr
M.Sc. Microbiology
India

IVD regulatory and product development specialist with 10+ years of experience in diagnostic virology, immunoassay development (ELISA, rapid te...

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USD 40/hr
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Soutik D.

Regulatory Affairs Specialist | Drug Dossier Compilation | CDSCO, USFDA, EMA | eCTD/CTD | Remote & Part-Time availab...
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USD 10/hr
Advanced Diploma
India

About Me I am a Regulatory Affairs professional with hands-on internship experience in the pharmaceutical sector, specializing in drug dossier ...

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USD 10/hr
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Emilie M.

Regulatory Consultant, PMS & Vigilance for Medical Devices & IVD
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USD 100/hr
Diploma in Clinical Research, Vigilance, and Post-Market Surveillance
France

I am a freelance consultant with over 10 years of experience in regulatory affairs, specializing in Post‑Market Surveillance (PMS) and vigilanc...

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USD 100/hr
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Dr. Jamila A.

MedTech Program Manager & SaMD Expert | FDA 510(k) · IVDR · IVD · Digital Health | 17+ Years
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USD 130/hr
PhD | Neuroimaging
France

I help MedTech companies bring regulated products to market — from early development through regulatory submission — with a particular focus on...

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USD 130/hr
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José Daniel C.

Medical Device Regulatory Affairs & Market Access Specialist | LATAM Health Policy
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USD 60/hr
Masters of Public Health
Colombia

Biomedical Engineer, Microbiologist, and Master of Public Health (MPH) with over 5 yea...experience in the global medical device industry and healthcare public affairs....

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USD 60/hr
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Dr. Adam S.

PhD Academic Writer | Dissertations | Thesis | Research Papers | Researcher | Scientific Writer | Editor | Proofreader
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USD 8/hr
Doctor of Education (EdD)
India

Former university professor & PhD-qualified academic consultant with 12 years of experience delivering publication-ready dissertations, the...

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USD 8/hr
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Dr. Elma H.

DVM, MSc & PhD Candidate | Scientific Consultant | 5 WoS Q1 & 64+ Pubs | Rapid Medical & Grant Writing
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USD 100/hr
Doctoral Candidate in Veterinary Sciences
Bosnia and Herzegovina

Elma Hrustemović, DVM, Academic Specialist in Clinical Microbiology and PhD Researcher, is a dedicated scientist at the University of Sarajevo,...

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USD 100/hr
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Andrei L.

Medical AI Solutions Architect | EU AI Act & MDR Compliance Expert | Custom RAG & Python Developer
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USD 100/hr
Engineering in Biotechnology
Romania

I bridge the gap between clinical requirements and advanced AI architecture. With a strong background in Healthcare & Medicine and deep tec...

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USD 100/hr
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Dr. Seval K.

Global Life Science Advisor – Quality Assurance & Controls - Regulatory Affairs - R&D - Production - Clinical Af...
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USD 280/hr
Chemistry PhD
Turkey

Quality Assurance , Validation Planning and Reporting , Medical Device Clinical Study Design and Reporting by CER PSUR and else. , FDA Register...

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USD 280/hr
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Dr. Abdullah O.

Innocentive solver ( 4 awards), Prof of Biochemistry and Clin. Biochem, Biogerontologist, Bioinformatician, 30+y exp, MD
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USD 95/hr
Master of Bioinformatics
United States

I seek opportunities where I can leverage my expertise in aging biology (biogerontology), biochemistry, clinical biochemistry, bioinformatics, ...

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USD 95/hr
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Kolabtree is the leading online marketplace for EU In vitro Diagnostic Regulation (IVDR) Compliance experts. Post your project, get bids, and hire qualified experts quickly and easily.

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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 the safety and security of your payments, personal information and project details. Kolabtree’s T&C include 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 aren'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 if 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 aren'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.

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.