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

Dr. Sarah C.

Consultant in Digital Health & Life Sciences | Chemist | Expert in Digital Health, Drug Discovery & Organic Che...
Create Project
★★★★★
☆☆☆☆☆
USD 50/hr
PhD (Chemistry)
Indonesia

Consultant to the digital health & life sciences industry with a strong research background in early stage drug discovery. I have extensive...

★★★★★
☆☆☆☆☆
USD 50/hr
Contact3

Dr. Imen S.

Quality mangement/Audit
Create Project
★★★★★
☆☆☆☆☆
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...

★★★★★
☆☆☆☆☆
USD 50/hr
Contact3

Dr. Vishal M.

Senior Scientist ★ Technology Consultant ★ Materials/Product Development ★ Innovator-serving Space, Medical &amp...
Create Project
★★★★★
☆☆☆☆☆
USD 100/hr
PhD-Material Science
United States

Technology focused accomplished Material Scientist with research and professional expertise in developing innovative materials solutions. As a ...

★★★★★
☆☆☆☆☆
USD 100/hr
Contact3

Dr. Paula P.

Medical Writer with 15+ years of experience in scientific writing
Create Project
★★★★★
☆☆☆☆☆
USD 75/hr
PhD in Pharmaceutical Sciences
Portugal

- Degree in Pharmaceutical Sciences, Faculty of Pharmacy, University of Porto (2000) - PhD in Analytical Chemistry, Faculty of Pharmacy, Univer...

★★★★★
☆☆☆☆☆
USD 75/hr
Contact3

Dr. Nadeem A.

Cell and Molecular Biologist | MBA in Medical devices and Healthcare Management | Certified in Regulatory Affairs - GxP
Create Project
★★★★★
☆☆☆☆☆
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...

★★★★★
☆☆☆☆☆
USD 80/hr
Contact3

Dr. Eric L.

Regulatory Affairs & Quality Assurance Consultant (Medical Devices)
Create Project
★★★★★
☆☆☆☆☆
USD 90/hr
Ph.D. Molecular Biology
Spain

With a strong scientific background, I bring extensive expertise in medical device development's regulatory and quality aspects. As an acco...

★★★★★
☆☆☆☆☆
USD 90/hr
Contact3

Dr. Harsh V.

Medical/Scientific/Regulatory/Newsletter/CMC/Dossier/Research/Review/Thesis/Protocol/Report/Article writing & editin...
Create Project
★★★★★
☆☆☆☆☆
USD 30/hr
PhD
India

A competent pharma professional with experience in Scientific writing, Regulatory competitive intelligence, DRA, F&D, MSAT and QA. Experie...

★★★★★
☆☆☆☆☆
USD 30/hr
Contact3

Dr. Sonia C.

Research and development, product development, program management, ISO 13485:2016, Medical Devices, In-vitro diagnostic
Create Project
★★★★★
☆☆☆☆☆
USD 120/hr
PhD Microbiology
France

I have been working for the health industry, In-vitro diagnostic and medical devices for over 20 years, mainly at R&D positions and alw...

★★★★★
☆☆☆☆☆
USD 120/hr
Contact3

Selina B.

Experienced medical writer
Create Project
★★★★★
☆☆☆☆☆
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 ...

★★★★★
☆☆☆☆☆
USD 70/hr
Contact3

Kavita S.

Experienced Medical Device Regulatory Affairs professional
Create Project
★★★★★
☆☆☆☆☆
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...

★★★★★
☆☆☆☆☆
USD 40/hr
Contact3

Michal H.

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

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

★★★★★
☆☆☆☆☆
Contact3

Pradip F.

R & D Expert, Scientific Advisor/Strategist/consultant with >20 years of experience in Lifesciences and Healthcar...
Create Project
★★★★★
☆☆☆☆☆
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...

★★★★★
☆☆☆☆☆
USD 30/hr
Contact3

Lakshman Prakash B.

experience in Lifesciences in QA, QMS, Regulatory, EU-IVDR, medical device documentation writing clinical trial reports
Create Project
★★★★★
☆☆☆☆☆
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...

★★★★★
☆☆☆☆☆
USD 100/hr
Contact3

Jacqueline V.

Clinical researcher (MICR) and Medical writer skilled in Clinical Evaluations MDR IVDR, PMS(PMSR/ PSUR) and PMCF plans
Create Project
★★★★★
☆☆☆☆☆
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...

★★★★★
☆☆☆☆☆
USD 120/hr
Contact3

Akhthar S.

Management Consultant maximizing clients profits through VALUE SELLING
Create Project
★★★★★
☆☆☆☆☆
USD 285/hr
MBA
United States

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

★★★★★
☆☆☆☆☆
USD 285/hr
Contact3

Tarun P.

Regulatory Expert (Consultant) having 25 years of experience working with Pharma, CRO and Medical Device Industry
Create Project
★★★★★
☆☆☆☆☆
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...

★★★★★
☆☆☆☆☆
USD 150/hr
Contact3

Sarah B.

Biostatistics consulting services & data analysis by industry experienced Biostatistician (Medical Statistician)
Create Project
★★★★★
☆☆☆☆☆
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...

★★★★★
☆☆☆☆☆
USD 130/hr
Contact3

William T.

Writer and Scientist skilled in project management, compliance, and high-throughput automation within CL3 environments.
Create Project
★★★★★
☆☆☆☆☆
USD 40/hr
MSc - Infection and Immunity
United Kingdom

Experienced Technical Writer and Laboratory Scientist adept at managing and executing multifaceted projects within stringent timelines. Profici...

★★★★★
☆☆☆☆☆
USD 40/hr
Contact3

Khalaf A.

QA Director & Regulatory Expert | GMP & ISO | Chemical Analysis & Process Optimization for Medical Devices |...
Create Project
★★★★★
☆☆☆☆☆
USD 40/hr
BA, Chemistry
Saudi Arabia

With a Bachelor of Science in Chemistry from King Saud University and a proven tenure as a Quality Director at Advance Medical Company, I posse...

★★★★★
☆☆☆☆☆
USD 40/hr
Contact3

Viky Gilles Daniel V.

Global Regulatory Affairs Consultant - FDA - Medical Device - Pharma
Create Project
★★★★★
☆☆☆☆☆
USD 150/hr
Global Regulatory Affairs Certification
United States

Guru providing regulatory affairs services to the medical device / medtech, biotech, and pharmaceutical industries. Qualification supported by ...

★★★★★
☆☆☆☆☆
USD 150/hr
Contact3

Kristen H.

Medical Writer with 5+ years of experience in systematic literature review, marketing, medical content writing
Create Project
★★★★★
☆☆☆☆☆
USD 45/hr
MA Athletic Training
United States

As a seasoned medical technical writer and chronic illness patient advocate, I am devoted to the meticulous translation of intricate medical in...

★★★★★
☆☆☆☆☆
USD 45/hr
Contact3

ADNAN A.

QA/RA Medical Devices Expert
Create Project
★★★★★
☆☆☆☆☆
USD 150/hr
BEng Hons Manufacturing Engineering
United Kingdom

20 years in Medical Devices, QA. RA, Validation for all Classifications of Medical Devices. MDR. IVDR expertise, with Software as a Medical Dev...

★★★★★
☆☆☆☆☆
USD 150/hr
Contact3

Andrew B.

Medical writer with 4+ years of experience in clinical evaluation
Create Project
★★★★★
☆☆☆☆☆
USD 50/hr
Master of Public Health
United States

Technical writer with 3 years’ experience executing clinical-regulatory documentation and demonstrated knowledge of EU MDR, clinical evaluation...

★★★★★
☆☆☆☆☆
USD 50/hr
Contact3

Dr. Loleta R.

Clinician innovator with 15+ years experience in data-driven strategy, medical diagnostics and bio-entrepreneurship
Create Project
★★★★★
☆☆☆☆☆
USD 90/hr
MBA Healthcare Administration
United States

Seasoned clinician innovator (MD, MBA) and data-driven strategist with unique healthcare and business acumen. Proficient in leading in-depth ma...

★★★★★
☆☆☆☆☆
USD 90/hr
Contact3

Michael L.

R&D Expert; Specializing in Laser Systems, IVF Microscopy, and Research Lab Digitalization
Create Project
★★★★★
☆☆☆☆☆
USD 140/hr
Executive certificate in Innovation management and entrepreneurship
Germany

I am an accomplished professional with a PhD in Optoelectronics and Laser Systems, along with an Executive Certificate in Innovation Management...

★★★★★
☆☆☆☆☆
USD 140/hr
Contact3

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.

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.

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.