Profile Summary
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...
Shiraz A.
Medical writer with experience in FDA/PAAB compliant promotional assets for HCP, Patient, and DTC audiences. Proficient in MLR submissions and...
Arnaz A.
Experienced in Biosimilars R&D development, fill-finish activities in manufacturing, primary & secondary packaging development ...
Jose A.
Behind every successful medical device registration, there is a team of experts working hard to ensure it meets regulatory requirements. As a Q...
Sarah B.
I'm a qualified Biostatistician with several years experience in the design and analysis of clinical studies including clinical trials. Thi...
Raju B.
Experienced toxicologist in risk assessment in various chemicals, ingredients, extractable and leachable and medical devices as per ISO, PDE, O...
Peter O.
Product experience includes Class 1, 2 and 3 devices: external defibrillators, AEDs, infusion pumps, patient monitors, image guidance, ventilat...
Vidur S.
Medical device executive with a results-oriented entrepreneurial drive. Dynamic, versatile and adaptable professional with 19 years of comprehe...
Judit P.
Scientist with lab experience in protein and antibody engineering, cancer and infectious diseases. Currently doing my PhD in advanced antibody ...
Daniel W.
Scientist with extensive management experience, including navigating the operational complexities of cross-functional and multi-PI collaboratio...
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....
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, ...
Eric D.
Over 25 years of experience in all facets of clinical research including with a focus on early phase medical devices and combination products. ...
Mohamad Marwan S.
I am a Biomedical Engineer with a strong background in medical device technology, neurotechnology, and AI-driven healthcare solutions. I am pur...
Megha B.
I have 15+ years of experience in health economics and outcomes research (HEOR) and market access in the US and globally. I have prepared healt...
QUYNH N.
EDUCATION: - Master in Science, Technology and Health - Sorbonne Université - France - Clinical Research Associate Certificate EXPERIENC...
Viktoria K.
I am an independent clinical research professional with 14 years experiences in the sector. My expert area is clinical trial protocol content r...
Deepa G.
➢Medical writing as per new regulation -Clinical (CEP, CER, Literature review, PMS plan etc) & Non-clinical documents (DOC, Risk Analys...
F H C.
I offer support for: Regulatory Affairs Clinical Trials and Trial Management Evidence-Based Medicines and Outcomes Research Non-clinical Develo...
Jenny V.
My background is nearly two decades in a clinical environment in medical imaging spread over the UK, New Zealand, Australia, and Timor Leste. ...
.webp)
Rayan T.
👩💼 I am a published scientific researcher. I currently work in academia at King's College London. My areas of expertise ar...
Ben C.
I'm a therapeutic goods industry professional, working within the Australian medical device and pharmaceutical manufacturing sectors since ...
Rakesh S.
Specialized Focus Areas: • Standards and Regulations of Medical Device ISO 13485 and 21 CFR part 82 • Sealing process characterization study ba...
Tara N.
Masters in Biomedical Sciences, biotech, pharma experience. ICH CORE AMA MEDDEV FDA. Scientific writing/editing, research regulatory CME
Alexey D.
Product Design - Design based on expertise from the manufacturing environment, we support engineering teams by providing guidance on best prac...
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.
