Profile Summary
Dr. Nischal P.
I am Dr. Nischal P.M., an accomplished healthcare professional with over 22 years of experience in the field. For the past 9 years, I have ded...
- Translational cell biology and neuroimmunology strategy, planning, and analysis - Designing research strategy for NIH and NSF grants: over $3...
Dr. Jonathan A.
Medical writer with experience in pharmacoeconomics, pharmaceutical policy, health policy, and health services research.
Dr. Danielle K. B.
I am a Clinical Research professional with 6 years of experience in the various therapeutic ares including Respiratory, Cardiology, Men's H...
Dr. Lefteris T.
Are you looking for an experienced professional to conduct systematic reviews for your project or train you in the process? Look no further. I ...
Dr. Kurtulus G.
I am a freelance medical, scientific, and technical writer with high-quality researches at Harvard Medical School proven by research papers pub...
I have more than 6 years experience (research and pharmaceutical industry) with a long track of success. My years as a researcher provided me ...
1-) experienced in optical sensors, design of illumination devices and fibre optic systems. 2-) I have experience in theoretical modelling and...
Dr. Nare S.
My science qualification is Ph.D. in pharmaceutical science. My writing qualifications: - Writing in the Sciences Certificate (Stanford Univers...
Dr. Muhammad M.
"Hello and welcome to my freelance profile! I am a scientific writer and product development specialist with several years of experience ...
Dr. Ron C.
I write evidence-based science, do biomedical research consultancy, and teach biomedical courses for various audiences. What can I do for you...
Dr. Archana N.
I am Scientific and Medical Writer with 12+ years experience in academic research and writing. I have a Ph.D. in Genetics from one of the top t...
Dr. Ahram Q.
My professional background is to technically write the Scientific content, assess the researcher in research work related to Bioinformatics and...
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Denise A.
Hi, I'm Denise! I'm a Regulatory Affairs Professional with over 10 years of experience and a Master's Degree in Regulatory Affairs....
Nida A.
An experienced clinical research and medical device Technical file writer who has certified on MEDDEV 2.7/1 Rev#4 documentation, EU MDR 2017/74...
Morgan B.
Freelance writer with over 7 years in clinical research. I've been involved in medical device trials, drug trials, investigator-initiated s...
Adam F.
I performed inspections and premarket approvals for FDA for 7.5 years. I am now a Senior Consultant operating out of Switzerland. I operate a...
Highly motivated Product Formulation Expert and Regulatory Affairs Expert in the following fields: Medical Devices ,Pharmaceuticals ,Dietary Su...
Girish H.
An accomplished, versatile, results-oriented clinical research professional with over 16 years of experience in the Pharmaceuticals & M...
Rudra P.
We are a Contract Research Organization (CRO) that focuses on advanced project management, clinical operations, medical writing, statistical an...
Dr. Hafsa I.
Medical Device Production Manager with 5 years of experience in device development - Technical file - Design File - Procurement - Technology De...
Dr. Vanshika S.
I am a published neuroscientist with collaborative research work appearing in journals like Oxford Academic's Cerebral Cortex and BMJ's...
Dr. Oyinkansola S.
Overview: As a dedicated Medical Doctor and accomplished Research Writer, I bring a unique blend of medical expertise and writing proficiency ...
Dr. Roy A.
I am a full professor at La Sagesse University and the head of the Mechatronics and Biomedical Engineering Departments. My research focuses on ...
Dr. Pavel O.
AI engineer. Full-stack developer. Physician. Academic.
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.
