Shiraz A.
Experienced Sr. Medical Writer with expertise in FDA/PAAB compliant promotional assets for HCP, Patient, and consumer audiences.
Ajay Kumar Reddy J.
MBA graduate with expertise in digital content management, quality control, user acceptance testing and market research associated with multipl...
Alemu M.
Medicaldevices/consultation/specification/review/manual development/biosensor/CRISPR/
Nathália B.
Researcher in translational medicine and biomedical with experience in Clinical Research, Translational Research, and Clinical Analyses, I am q...
Arnaz A.
Experienced in Biosimilars R&D development, fill-finish activities in manufacturing, primary & secondary packaging development ...
Jose A.
Behind every successful medical device registration, there is a team of experts working hard to ensure it meets regulatory requirements. As a Q...
Arjun L.
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....
Alfredo M.
Medical Doctor (MSc in Stem Cells & Regenerative Medicine) specializing in tissue engineering, bioprinting, and biomaterials. CEO of Neoti...
Ana Sofia C.
I am an English to Portuguese Medical Translator and Writer working with Life Sciences companies, Contract Research Organizations, Language Ser...
Vidur S.
Medical device executive with a results-oriented entrepreneurial drive. Dynamic, versatile and adaptable professional with 19 years of comprehe...
Peter O.
Product experience includes Class 1, 2 and 3 devices: external defibrillators, AEDs, infusion pumps, patient monitors, image guidance, ventilat...
Judit P.
Scientist with lab experience in protein and antibody engineering, cancer and infectious diseases. Currently doing my PhD in advanced antibody ...
Raju B.
Experienced toxicologist in risk assessment in various chemicals, ingredients, extractable and leachable and medical devices as per ISO, PDE, O...
Megha B.
I have 15+ years of experience in health economics and outcomes research (HEOR) and market access in the US and globally. I have prepared healt...
Viktoria K.
I am an independent clinical research professional with 14 years experiences in the sector. My expert area is clinical trial protocol content r...
QUYNH N.
EDUCATION: - Master in Science, Technology and Health - Sorbonne Université - France - Clinical Research Associate Certificate EXPERIENC...
Mohamed S A.
Aspiring Machine Learning Engineer with a solid foundation in machine learning principles and hands-on project experience. Eager to contribute ...
Georgios A.
Passionate and motivated chemical-process engineer with demonstrated experience in validation strategy design, establishing validation master p...
Mizan H.
I am a public health professional and data scientist with expertise in research, health care costing, data analysis, and project management My ...
Tamil S.
5 years experience as an Quality Assurance professional.I have a broad background, topics include: - ISO 13485:2016 - 21 CFR 820 - ISO 14971, ...
Anna H.
Computational neuroscience researcher specialising in BCI, EEG analysis, and sensorimotor rehabilitation with expertise in clinical application...
Katrina L.
I am a biomedical scientist with a broad range of experience from academia, industry, and government. - Self-starter with project management an...
Alberto L.
I am a board-certified neurologist with over a decade of clinical and research experience. After completing my Neurology residency with honors ...
Deepa G.
➢Medical writing as per new regulation -Clinical (CEP, CER, Literature review, PMS plan etc) & Non-clinical documents (DOC, Risk Analys...
Jenny V.
My background is nearly two decades in a clinical environment in medical imaging spread over the UK, New Zealand, Australia, and Timor Leste. ...
Hire medical device consultants for help with FDA approvals, 510(k) submissions, EU MDR compliance and more. Get end-to-end product development support. Work with medical device engineering consulting experts for help with content writing and medical copywriting.

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Hire medical device freelancer for FDA approval$500.00
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hire medical device engineering consultants for EU MDR$400.00
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What Does a Medical Device Engineering Consultant Do?
A medical device consultant works with medtech companies to help them develop and design products, meet regulatory requirements, conduct clinical trials and market the product. A medical device expert can have 10-20 years of experience in the field in the areas of compliance and product design. A medical device writer can help with regulatory documents such as FDA submissions, Clinical Evaluation Reports, clinical trial protocols, and grants, as well as with content writing requirements such as white papers, blog articles and press releases. Companies worldwide are increasingly seeking medical device expertise on demand as it allows the flexibility of hiring remote workers as and when required.
Why Approach Experts Instead of a Medical Device Consultancy?
Medical device companies have typically used a medical device consultancy to outsource their tasks. However the freelance revolution has made it possible for them to hire experts for short-term or contract projects. Hiring experts directly requires no minimum commitment or contract. A medical device engineering consultant freelancer can provide a variety of services ranging from literature search and systematic reviews to statistical analysis and clinical research. On Kolabtree, it's quick and easy to directly contact a freelancer and have one-to-one conversations about your requirements.
How Medical Device Writing Experts Can Help
A medical device writing expert can provide a wide range of services that help medtech SMBs save precious time and energy. These include but are not limited to:
- Developing 510(k) submissions for FDA approval
- Developing CERs, clinical research protocols, and clinical case studies
- Putting together grant applications and proposals
- Writing and reviewing blog articles, website content, white papers and ebooks
- Writing and editing research papers and preparing them for journal publication
Working with a medical device writing consultant is becoming an increasingly popular choice among medtech businesses so that they can streamline their resources. With scientists and industry experts working remotely, it's possible to access medical device expertise in domains like cardiology, orthopedics, medical imaging, and more.
As a Medical Device Company, What Functions Can You Outsource?
From ideation to product marketing, medical device engineering consultants can work with you at every stage of the product cycle. A medical equipment consultant can improve and optimize the design of equipment such as MRIs, ultrasound machines, etc. Biomedical engineers can work on a contract basis to provide prototypes and the final product design. A medical device marketing freelancer can develop creative campaigns and brand messaging to position your product in the market. A medical device development freelancer is typically an experienced expert, who can help with validation, verification, testing and compliance of the product. Medical writing is one major function that can easily be outsourced to qualified experts: a medical device writing freelancer can develop compelling, authoritative copy for your target audience.
How Much Does It Cost to Hire Medical Device Experts?
The hourly rate for hiring medical writers on Kolabtree is $40 to $70. The fee for your project will depend on the expertise required, how urgently the work is needed, and what level of speciality you're looking for. Medical device consultants who work on design, development and compliance can charge up to $300 per hour. On Kolabtree, you can discuss your requirements directly with experts and get a range of quotes before choosing the best expert based on your budget and timeline.
Hire Medical Device Engineers by posting a project for free.