Profile Summary
Deepa G.
➢Medical writing as per new regulation -Clinical (CEP, CER, Literature review, PMS plan etc) & Non-clinical documents (DOC, Risk Analys...
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. ...
Rakesh S.
Specialized Focus Areas: • Standards and Regulations of Medical Device ISO 13485 and 21 CFR part 82 • Sealing process characterization study ba...
Ben C.
I'm a therapeutic goods industry professional, working within the Australian medical device and pharmaceutical manufacturing sectors since ...
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...
Rob F.
Rob is a Quality System and Regulatory professional with over 20 years of experience in QMS development, deployment, and remediation in the med...
Soundarya P.
Handled more than 30 clinical evaluation reports end to end, starting from clinical evaluation plan, literature screening, literature summaries...
Mawaddi Q.
A clinical Evaluation specialist with clinical, research and occupational audiology background. I'm passionate in clinical research and any...
Ellen S.
A dedicated and driven professional with a diverse background in biotech and a strong foundation in project management and scientific consultin...
João M.
I’m a biochemist specialized in materials science; I have over 15 years experience in a mixed context of academic and industrial environments, ...
Nicole R.
Motivated, customer-focused Project Manager within the Cardiovascular, Metabolic and Critical Care Department who has more than 16 years of exp...
Prerana D.
A clinical research post-graduate having a vast knowledge over a range of Medical devices consulting services on conformation of 62304:2006 sta...
Rukmani S.
I am a biomedical research scientist and a science communicator based in Ireland with over 8 years experience writing/editing manuscripts, prep...
Kristen H.
As a seasoned medical technical writer and chronic illness patient advocate, I am devoted to the meticulous translation of intricate medical in...
Asma S.
A dynamic result-oriented professional holding a noteworthy 7+ years of diversified experience in the area of Intellectual property analysis an...
Andrew B.
Technical writer with 3 years’ experience executing clinical-regulatory documentation and demonstrated knowledge of EU MDR, clinical evaluation...
Boris L.
I prepare and prosecute patent applications with the USPTO and internationally
Ninja P.
An aspirational mind whose main interest is to pursue a career and advance in Regulatory Affairs and Quality Assurance, become part of an este...
Viky Gilles Daniel V.
Guru providing regulatory affairs services to the medical device / medtech, biotech, and pharmaceutical industries. Qualification supported by ...
Sonia M.
Sales manager with experience in claim resolution
Khalaf A.
With a Bachelor of Science in Chemistry from King Saud University and a proven tenure as a Quality Director at Advance Medical Company, I posse...
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...
Giovanni N.
Agile industrial engineer with five years of experience in medical devices manufacturing. Strong capabilities for risk management, continuous i...
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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You can choose to pay either a fixed or an hourly fee based on your requirement.
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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.
