Profile Summary
Erik M.
10 years of Quality and Regulatory experience in the medical device industry. During my career, I have been a key player in the development and...
Nandhini K.
I am Nandhini, KM, Dentist, and a professional Medical Content Writer. I can assure you to provide quality content in the field of medicine wit...
Lakshman Prakash B.
Experience in Lifesciences industry including over 18 years’ experience in QA, QMS, Regulatory, Manufacturing, Quality Unit (Commissioning, Qua...
Tarun S.
Medical device professional with strong background in single use disposables, reusable medical devices(Class I, Class II and Class III) . Broad...
Jacqueline V.
Registered healthcare professional with 16 years of clinical experience in academic hospitals and clinical research. Trained in Clinical Evalua...
Ajay C.
I am Mechanical engineer with 16 years of experience in R&D, New product design and development, Innovation for Medical devices, Consum...
Pranay V.
With more than 5+ years of experience in MEDICAL DEVICE industry, I have developed many devices, regulations, SOP's as per quality standard...
Vaibh K.
Medical device risk assessment
Marin L.
Leading medical strategy in matrix-based global environment and providing scientific and business consultation to a local and global pharmaceut...
Alemu M.
Medicaldevices/consultation/specification/review/manual development/biosensor/CRISPR/
Tarun P.
Vision-driven executive with over 25 years of demonstrated leadership in the pharmaceuticals industry. Proven track record of driving bold init...
Jason B.
With 10+ years of experience in medical device design experience, I can commit myself to helping startups to develop their own product ideas, d...
Ajay Kumar Reddy J.
MBA graduate with expertise in digital content management, quality control, user acceptance testing and market research associated with multipl...
Arnaz A.
Experienced in Biosimilars R&D development, fill-finish activities in manufacturing, primary & secondary packaging development ...
Sarah B.
I'm a qualified Biostatistician with several years experience in the design and analysis of clinical studies including clinical trials. Thi...
Vidur S.
Medical device executive with a results-oriented entrepreneurial drive. Dynamic, versatile and adaptable professional with 19 years of comprehe...
Peter O.
Product experience includes Class 1, 2 and 3 devices: external defibrillators, AEDs, infusion pumps, patient monitors, image guidance, ventilat...
Ana Sofia C.
I am an English to Portuguese Medical Translator and Writer working with Life Sciences companies, Contract Research Organizations, Language Ser...
Arjun L.
I have a blend of experience in clinical medicine, pharmaceutical industry and medical device industry....As a medical doctor, I work on infectious diseases, pulmonary and critical care and public health....
Judit P.
Scientist with lab experience in protein and antibody engineering, cancer and infectious diseases. Currently doing my PhD in advanced antibody ...
Raju B.
Experienced toxicologist in risk assessment in various chemicals, ingredients, extractable and leachable and medical devices as per ISO, PDE, O...
Michael L.
I am an accomplished professional with a PhD in Optoelectronics and Laser Systems, along with an Executive Certificate in Innovation Management...
Nathália B.
Biomedical with experience with clinical and translational research
QUYNH N.
EDUCATION: - Master in Science, Technology and Health - Sorbonne Université - France - Clinical Research Associate Certificate EXPERIENC...
Tamil S.
5 years experience as an Quality Assurance professional.I have a broad background, topics include: - ISO 13485:2016 - 21 CFR 820 - ISO 14971, ...
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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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 arn’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.
