Profile Summary
Jean M.
Clinical data and biometrics leader with 20+ years of experience across global clinical trials, from Phase I to pivotal studies. Specialized in...
Shaheen Fathima A.
Regulatory documentation either moves a program forward or it doesn't. I make sure it does. I'm a RAC-Drugs certified Regulatory Affai...
Dr. Sumit M.
I am a medical doctor (MBBS) and certified clinical researcher specialized in high-stakes regulatory documentation and clinical trial design. M...
Dr. Martin S.
I help medical device and digital health companies bring their products to regulatory readiness in the UK (MHRA, UK MDR 2002), with a focus on ...
Dr. Yanping G.
Board-certified Pathologist and Clinical Chemist with 17 years of experience as a clinical laboratory director. Experience and insights in path...
Dr. Graig-David S.
Graig-David Snyders senior-level scientific and engineering generalist specializing in the intersection of biomedical signal processing, medica...
Dr. Peter O.
I have published a number of review and research articles in journals of international repute, while I currently serve as a reviewer to top-not...
Dr. Martina M.
Biomedical engineer with a joint PhD from Ghent University and the University of Genova, specializing in biomaterials, hydrogel systems, and ti...
Dilini H.
I am a qualified Cardiology Technologist with over 10 years of experience in the healthcare sector, specializing in cardiovascular diagnostics ...
Dr. Muhammad Arfat Y.
I am a seasoned researcher and academic professional with over two decades of experience in pharmaceutical sciences, microbiology, and clinical...
Dr. Gabrielle R.
I am an experienced medical writer and clinical psychologist. I have a Ph.D. and a master's degree from The University of Texas at Austin. ...
Marko K.
Pharmacist | Regulatory Affairs & Clinical Compliance Specialist Experienced pharmacist with a background in GDP logistics, medical device...
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MAHMOUD A.
Results-driven Biomedical Clinical Engineer with over 14 years of hands-on experience in the installation, maintenance, and troubleshooting of ...
Dr. Dominique E.
Senior Human Factors and UX Researcher with a PhD in Industrial and Systems Engineering (Human-Centered Systems). Approximately 8 years of mixe...
Sruthi P.
I am a physician with an MD in Respiratory Medicine, with expertise in pulmonary diseases, clinical evaluation, evidence-based medicine, and sc...
Dr. Sebastian M.
I am a computational neuroscientist and biostatistician with a PhD in Biology and Neuroscience and over a decade of experience analyzing comple...
Dr. Christoph P.
Most startups realize too late: getting a digital health product from concept to CE mark is as much a regulatory journey as a technical one. I...
Dr. Pedro Emmanuel B.
I am a Senior Clinical Epidemiologist and Academic Researcher with extensive experience in clinical research, infectious diseases, and public h...
Dishan O.
I am a Mechatronics Engineer with expertise in biomedical engineering, artificial intelligence, computer vision, embedded systems, and medical ...
Dr. Amin J.
Biomedical Engineer (PhD) specializing in Medical Devices, Regulatory Writing, and Clinical Evaluation. Experienced in preparing CER, MDR‑compl...
Towanda L.
Regulatory Affairs: FDA submissions, EU MDR technical files, Post-Market Surveillance Reports (PSURs), and Declarations of Conformity. Quality...
Dr. Narimane K.
Pharmaceutical and biotech companies are increasingly adopting New Approach Methodologies (NAMs), yet many still face challenges in selecting t...
Dr. Omar Antonio P.
Biomedical engineer and MedTech leader with 8+ years building and scaling regulated Software as a Medical Device (SaMD) at the intersection of ...
Dr. Bernardas J.
I am a CFD and simulation specialist with a PhD in Engineering and industrial experience spanning engineering consultancy, product development ...
Dr. Reza H.
I am an award-winning Analytical Chemist and Senior Scientist with 15+ years of experience in immunoassay development, biosensors, bioconjugati...
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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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.
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You have to approve the deliverables only if quality meets your expectations. If you aren't happy, we'll refund your money.
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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.