Ayoub B.
I am a trilingual Biomedical Engineer (French/English/Arabic) with dual academic training from UTC Compiègne (France) and ENSAM Rabat (Mor...
Camila V.
Experienced in therapeutic guidance, special medications, pharmacovigilance, and critical analysis of clinical protocols. As a consultant, I br...
Noor A.
Noor Abu Hantash is a medical student at Jordan University and an aspiring researcher in medical topics, specifically cardiothoracic surgery. ...
Dr. Somnath Swami V.
Researcher with expertise in solubility enhancement and formulation development of pharmaceutical compounds, focusing on the use of mesoporous ...
Nathaniel Jonathan B.
Venture architect based between Zurich and Prague, I help private clinics, biotech startups, and UHNW health ventures launch with clarity, ethi...
Devin M.
I help medtech companies design, assess, and improve quality systems to ensure regulatory compliance, streamline development, and prepare for a...
Dr. Mohsen M.
I’m a biomedical engineer (PhD) with over 15 years of cross-functional experience in medical device development, neurotechnology, and regulator...
Dr. Alexandra A.
With 16 years of industry and academic experience combined in the medical device and interventional oncology fields, I am passionate about alig...
Kathleen D.
👩🏻💼 Who I Am: Seasoned QMS and Compliance consultant dedicated to helping organizations achieve operational excellence...
Dr. Yevheniia B.
I am a scientific reviewer and editor with a PhD in Agricultural Sciences and a strong background in biology, human and animal physiology, and ...
Madalina C.
I am a certified physiokinetotherapist with a multidisciplinary academic background and professional experience in medical rehabilitation, educ...
Wim V.
I am an experienced independent consultant specializing in clinical research management for medical devices, with a focus on EU MDR compliance,...
Sarah M.
I’m a PhD-trained scientific writer...and editor with deep expertise in life sciences and a proven track record of delivering high-impact publications...
Dr. Kathryn O.
Scientist with over 10 years of proven research experience in preclinical and clinical settings working independently to design, optimize and e...
Dr. Karla R.
biomedical engineer and AI consultant with 10+ years of experience in research, development, and implementation of digital health solutions, me...
Dr. Steininger C.
I am an experienced life sciences professional with a strong interdisciplinary background at the intersection of science, diagnostics, and entr...
Katherine A.
Katherine Antoniak, MPH, is a healthcare and medical education leader with deep expertise in clinical research, surgeon education, and emerging...
Kristen D.
Innovative executive in clinical operations and regulatory affairs with successful experience in start-ups, hospital & CROs, private equity...
Dr. Thomas P.
I am a recently graduated biomedical engineering PhD with a specialty in the design, development, and testing of medical devices. My thesis foc...
Mohamed H.
I am a Clinical Research Professional with over 13 years of global experience in clinical trial management, medical writing, and regulatory sub...
Dr. Anand kumar P.
ISO 42001 ARTIFICIAL INTELLIGENCE SYSTEM IMPLEMENTATION | ISO 13485 FOR MEDICAL DEVICES | ISO27001 FOR MENTAL HEALTH PRODUCT | HIPAA GDPR COMPL...
Rajesh K.
I am a freelance Research Toxicologist with 5 years of experience in preclinical toxicity studies, specializing in acute, subacute, subchronic,...
Woodrow S.
I am a Certified Quality Engineer and ISO 13485-trained Lead Auditor with a background in biomedical engineering and hands-on experience leadin...
Dr. Andrea H.
I’m a PhD-trained biomedical engineer and educator with over 20 years of experience advancing inclusive innovation in health, education, and gl...
Ahmed Y.
I am a professional chemist with strong expertise in biochemistry, physical, organic, and analytical chemistry. My background combines both sci...
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.