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Hire a Medical Device Regulations Expert

Masters program about drug development
Spain
USD55.0 per hour
MDR Consultant / CER writer

I have more than 6 years experience (research and pharmaceutical industry) with a long track of success. My years as a researcher provided me ...

PhD
United States
USD75.0 per hour
Freelance CER Writer | Science and Medical Communications Specialist | Neurospsychiatry Expert | Creative Writer

I am a freelance science and medical writer catering to a diverse audience of scientists, healthcare professionals, pharmaceutical and medical ...

B.Pharmacy
India
USD40.0 per hour
Freelance Medical Writer / Expert in Medical Device with 13 Years of Experience in Clinical Research (MDR Expert)

An accomplished, versatile, results oriented clinical research professional with over 12 years of experience in the Pharmaceuticals & M...

Master of Public Health (M.P.H.), Introduction to Systematic Review and Meta-Analysis
India
USD90.0 per hour
Freelance medical writer, CER writer, MDR Consultant, Scientist, 21 years experience in clinical research, manuscripts.

A top rated writer & editor with emphasis on medical writing, scientific journal manuscripts, public health, environmental science and ...

Master of pharmacy
India
USD25.0 per hour
Experienced medical writer/ MDR consultant

I am medical writer with more than 5 years of experience in writing regulatory and clinical research document. My expertise is development of c...

PhD, Epidemiology
United States
USD0.0 per hour
Experienced real-world researcher, generating evidence from clinical data for medical devices and pharmaceuticals.

Mary Beth Ritchey, PhD, FISPE has spent more than 15 years in government, industry, consulting, and academia in better understanding medical pr...

PhD Engineering
United Kingdom
USD50.0 per hour
Medical Devices R&D | Validation and Verification following Q/RA | Computational simulation applied to MD

Doctor in Engineering specialised in medical devices research and development. Focused on validation and verification of development processes ...

Master of Science
United States
USD85.0 per hour
Experienced CER Writer

My expertise is development of clinical evaluation reports (CERs). This includes experience with literature searches, post-market surveillance,...

PhD cum laude. Medical Physics
Netherlands
USD70.0 per hour
Data science, machine learning, medical imaging, physicist. 15+yrs clinical research. Medical device development.

PhD, postdoc, senior researcher in medical physics, imaging, radiotherapy. Extraction of attributes from real-world collected data. Medical Im...

PhD
Australia
USD70.0 per hour
Principal consultant, Weiss Communications

* Ten years of writing experience in molecular biology, protein chemistry, cell biology and microscopy across three countries. * Six years of s...

Certificate in Leadership & Performance Management
South Africa
USD100.0 per hour
PhD in medical science with 30+ years of academic and clinical research industry experience

I provide consulting, medical writing and training services to Pharma, Biotechnology Companies, CROs, NGOs, Foundations and the clinical resear...

MS in Regulatory affairs
Canada
USD40.0 per hour
Regulatory affairs, Quality assurance and a medical writer with 13+ experience in medical device and pharma industry

Accomplished pharmaceutical and medical device regulatory and quality professional with over 12 years experience in regulatory compliance, prod...

B.E. Mechanical engineering
India
USD10.0 per hour
Expert in EU MDR and EU MDD Remediation and Gap assessments.

MDR and MDD Gap assessments and Remediation. Risk documents creation and all remediation process knowledge to get the CE mark for the product t...

Diploma in Quality Auditing
Australia
USD150.0 per hour
Therapeutic Goods Consultant: Quality Systems, Regulatory Affairs, Auditing, Product Development and Validations

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

Master's degree Pathology/Pathologist
China
USD20.0 per hour
Freelance medical writer providing writing service in English and Chinese | Medical writing/translation/proof-reading

- Graduate with a Master of Medicine degree from Nanjing Medical University, China - Independent and team-based technical/medical writer, famil...

Bachelor of Science Electronic Engineering
United States
USD50.0 per hour
Electrical Engineer: Medical Device R&D, Telecom product development, regulatory compliance

14 years of experience as an Electrical Engineer working in Medical Devices and Telecom for large organization and startups. * Drafting and rev...

Masters of Pharmacy
India
USD45.0 per hour
Scientific writer with 3+ years of hands-on experience in developing and reviewing clinical evaluation reports-MDD&M...

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

PhD (Chemical & Biomedical Engineering)
Singapore
USD50.0 per hour
MedTech innovator, Entrepreneur & Scientist

Researcher with 9+ years of experience working with nanomaterials and medical devices. Skilled in Research and Development (R&D), desig...

MBA
India
USD40.0 per hour
Experienced CER writer

Authored medical device registration submissions (CERs) to international regulatory bodies (EU NBs) while ensuring regulatory compliance across...

Biomedical Engineering
India
USD10.0 per hour
https://www.linkedin.com/in/kalidoss-p-09353a65

Work experience in Medical device regulatory, cybersecurity of the medical device, clinical evaluation report analysis, risk benefit analysis.

BE
India
USD10.0 per hour
2.3 years experience in Eumdr. As a part of MDR, I'm doing freelance work in writing CER and preparing EU Technical doc.

I'm an Engineering graduate having around 7 yrs experience with expert knowledge in EUMDR.

Masters degree in Biomedical Science
United States
USD110.0 per hour
CER Medical Writer/Associate Project Manager

A clinical research scientific writer with medical and regulatory CER expertise in MEDDEV 2.7/1 rev4 documentation, EU MDR and FDA compliance. ...

M.Sc Biochemistry
India
USD100.0 per hour
experience in Lifesciences in QA, QMS, Regulatory, EU-IVDR, medical device documentation writing clinical trial reports

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

Bachelors of Science in Biochemistry
Switzerland
USD500.0 per hour
exFDA Investigator / expert in Medical Device & Combination Product design, manufacturing, and compliance

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...

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