Profile Summary
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...
An aspirational mind whose main interest is to pursue a career and advance in Regulatory Affairs and Quality Assurance, become part of an este...
Technical writer with 3 years’ experience executing clinical-regulatory documentation and demonstrated knowledge of EU MDR, clinical evaluation...
Giovanni N.
Agile industrial engineer with five years of experience in medical devices manufacturing. Strong capabilities for risk management, continuous i...
Soundarya P.
Handled more than 30 clinical evaluation reports end to end, starting from clinical evaluation plan, literature screening, literature summaries...
Dr. Loleta R.
Seasoned clinician innovator (MD, MBA) and data-driven strategist with unique healthcare and business acumen. Proficient in leading in-depth ma...
Materials scientist with specialization in plastics design, analysis, processing and longevity, particularly in medical plastics and birth cont...
I have 15 years of experience in the field of Public Health and Clinical Research in several positions: coordination, monitoring, project man...
Medical devices professional with more than 25 years' experience in senior management positions in early stage medical device companies. A...
• Experienced Clinical research professional, with the strong academic foundation of Graduation in Pharmacy and Post-graduation in Biochemical ...
ChemicalQDevice CEO Kevin Kawchak has served as a Consultant in both the Academic and Industrial Chemicals setting. Over the course of his care...
Pharmaceutical Chemist with over 10 years of experience within diverse areas of the pharmaceutical and medical devices industries, mostly focus...
5+ years of experience in scientific research, 10+ peer-reviewed/under review publications on topics related to trauma implant performance, fra...
Dr Ashwani G.
A medical doctor with a Masters in Business Creation & Entrepreneurship from University of Tromso. 8+ years of experience which include...
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.
Bárbara S.
I’m a recent Master in Biomedical Engineering by the University of Minho. In the master's degree, I specialized in Biomaterials, Rehabilita...
Over 35 years of broad experience as Engineering professional…Medical Device Product Regulatory Requirements, Product Design, Project Managemen...
Clifford T.
Medical technology and medical education marketing consultant and PR specialist, specializing in the cardiovascular field. Also, published jour...
15 years of medical device experience Medical imaging, technologies Medical device business, marketing Financial literacy
Consulting services including application of IEC/EN 60601-1, IEC 62304, IEC 62366, ISO 14971. Project Management - Medical Devices Compliance. ...
Viky Gilles Daniel V.
Guru providing regulatory affairs services to the medical device / medtech, biotech, and pharmaceutical industries. Qualification supported by ...
Being an analyst and an expert writer, my first concern is to be perfectly fulfill my responsibilities with no delusion. My previous research w...
Natalie D.
I’m an ex-registered nurse, turned copywriter. I write marketing materials and patient education resources for the health and medical industry....
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.
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