Profile Summary
Lorenzo V.
Experience with laparoscopic, endoscopic, drug delivery (including combo devices), orthopedic implants and instruments (hip, knee, shoulder, fo...
Steve N.
Materials scientist with specialization in plastics design, analysis, processing and longevity, particularly in medical plastics and birth cont...
Mike P.
I can execute a scientific study from start to finish: • Study design • Full-stack development of an app for the...study • IRB approval • Participant recruiting • Study administration • Data analysis • Peer-reviewed publication...
Giovanni N.
Agile industrial engineer with five years of experience in medical devices manufacturing. Strong capabilities for risk management, continuous i...
Dr. Loleta R.
Seasoned clinician innovator (MD, MBA) and data-driven strategist with unique healthcare and business acumen. Proficient in leading in-depth ma...
Nisha N.
• Experienced Clinical research professional, with the strong academic foundation of Graduation in Pharmacy and Post-graduation in Biochemical ...
Assaf G.
Medical devices professional with more than 25 years' experience in senior management positions in early stage medical device companies. A...
Mariem R.
I have 15 years of experience in the field of Public Health and Clinical Research in several positions: coordination, monitoring, project man...
Mohan M.
Over 35 years of broad experience as Engineering professional…Medical Device Product Regulatory Requirements, Product Design, Project Managemen...
Dr Ashwani G.
A medical doctor with a Masters in Business Creation & Entrepreneurship from University of Tromso. 8+ years of experience which include...
Pharmaceutical Chemist with over 10 years of experience within diverse areas of the pharmaceutical and medical devices industries, mostly focus...
Baris O.
15 years of medical device experience Medical imaging, technologies Medical device business, marketing Financial literacy
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...
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.
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...
Chunnan C.
An experienced professional with 20 years of industrial experience in MedTech, biopharmaceutical companies and semi-governmental organizations;...
Natalie D.
I’m an ex-registered nurse, turned copywriter. I write marketing materials and patient education resources for the health and medical industry....
Michael L.
I am an accomplished professional with a PhD in Optoelectronics and Laser Systems, along with an Executive Certificate in Innovation Management...
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...
Ali H.
Consulting services including application of IEC/EN 60601-1, IEC 62304, IEC 62366, ISO 14971. Project Management - Medical Devices Compliance. ...
Clifford T.
Medical technology and medical education marketing consultant and PR specialist, specializing in the cardiovascular field. Also, published jour...
Erwan S.
4+ years of experience managing and executing marketing, pricing and sales strategy projects for C-level clients in LifeSciences multinationals...
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.
