Mariem R.
I have 15 years of experience in the field of Public Health and Clinical Research in several positions: coordination, monitoring, project man...
Assaf G.
Medical devices professional with more than 25 years' experience in senior management positions in early stage medical device companies. A...
Mohan M.
Over 35 years of broad experience as Engineering professional…Medical Device Product Regulatory Requirements, Product Design, Project Managemen...
Baris O.
15 years of medical device experience Medical imaging, technologies Medical device business, marketing Financial literacy
Pharmaceutical Chemist with over 10 years of experience within diverse areas of the pharmaceutical and medical devices industries, mostly focus...
Elaine S.
Extensive experience in orthopedic biomedical research, data analysis, manuscript writing and editing, CEP/CER writing for EU MDR, and systemat...
Bárbara S.
I’m a Biomedical Engineer who developed a great interest in Data Analysis and Visualization. In the projects I’ve been working on, I’ve been es...
Dr Ashwani G.
A medical doctor with a Masters in Business Creation & Entrepreneurship from University of Tromso. 8+ years of experience which include...
Natalie D.
I’m an ex-registered nurse, turned copywriter. I write marketing materials and patient education resources for the health and medical industry....
Wania H.
Being an analyst and an expert writer, my first concern is to be perfectly fulfill my responsibilities with no delusion. My previous research w...
Kevin Wilson M.
I have over 15 years of experience in consulting, pharma, and medtech. Currently I lead a consulting firm that helps life sciences companies to...
Kalidoss P.
Work experience in Medical device regulatory, cybersecurity of the medical device, clinical evaluation report analysis, risk benefit analysis.
Karthickeyan V.
I'm an Engineering graduate having around 7 yrs experience with expert knowledge in EUMDR.
William T.
Experienced Technical Writer and Laboratory Scientist adept at managing and executing multifaceted projects within stringent timelines. Profici...
Michael L.
I am an accomplished professional with a PhD in Optoelectronics and Laser Systems, along with an Executive Certificate in Innovation Management...
Chunnan C.
An experienced professional with 20 years of industrial experience in MedTech, biopharmaceutical companies and semi-governmental organizations;...
Kevin K.
ChemicalQDevice CEO Kevin Kawchak has served as a Consultant in both the Academic and Industrial Chemicals setting. Over the course of his care...
Clifford T.
Medical technology and medical education marketing consultant and PR specialist, specializing in the cardiovascular field. Also, published jour...
Ali H.
Consulting services including application of IEC/EN 60601-1, IEC 62304, IEC 62366, ISO 14971. Project Management - Medical Devices Compliance. ...
Veer P.
A seasoned IVDR Regulatory Affairs Professional with hands-on experience in Technical Documentation (STED/TD) preparation, Technical file prepa...
John W.
Your idea only matters if you can get it funded or commercialized. I am an experienced MedTech sales leader who's helped take a start-up fr...
Elham A.
Cultivated, adept engineering professional specializing in Manufacturing and Research and Development (R&D). Proven track record of Product...
Erwan S.
4+ years of experience managing and executing marketing, pricing and sales strategy projects for C-level clients in LifeSciences multinationals...
Michael B.
30+ years experience in MedTech. NICE MedTech Early Technology Assessment (NICE MetaTOOL) facilitator. Proven record in getting great technolog...
Biomedical E.
I am Umair Ahmed, a seasoned Biomedical Engineer and Scientist offering over 7 years of comprehensive experience in the freelance medical devic...
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.
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.
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.
-
Hire medical device freelancer for FDA approval$500.00
-
hire medical device engineering consultants for EU MDR$400.00
Post your Project (Free)
Your project details are safe, secure and visible only to logged-in users.
Get Quotes & Choose Experts
Discuss your requirements in detail with the experts before accepting the final statement of work from Kolabtree.
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.
Job Done!
Approve the deliverables once you're satisfied with the job done.
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.