Profile Summary
Haralabos P.
Working as a medical translator for the past 19 years (9 years full time), I have translated a wide range of biomedical documents including med...
➢Medical writing as per new regulation -Clinical (CEP, CER, Literature review, PMS plan etc) & Non-clinical documents (DOC, Risk Analys...
My background is nearly two decades in a clinical environment in medical imaging spread over the UK, New Zealand, Australia, and Timor Leste. ...
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...
I'm a therapeutic goods industry professional, working within the Australian medical device and pharmaceutical manufacturing sectors since ...
Masters in Biomedical Sciences, biotech, pharma experience. ICH CORE AMA MEDDEV FDA. Scientific writing/editing, research regulatory CME
Specialized Focus Areas: • Standards and Regulations of Medical Device ISO 13485 and 21 CFR part 82 • Sealing process characterization study ba...
Product Design - Design based on expertise from the manufacturing environment, we support engineering teams by providing guidance on best prac...
Rob is a Quality System and Regulatory professional with over 20 years of experience in QMS development, deployment, and remediation in the med...
I offer support for: Regulatory Affairs Clinical Trials and Trial Management Evidence-Based Medicines and Outcomes Research Non-clinical Develo...
Rukmani S.
I am a biomedical research scientist and a science communicator based in Ireland with over 8 years experience writing/editing manuscripts, prep...
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...
Experienced toxicologist in risk assessment in various chemicals, ingredients, extractable and leachable and medical devices as per ISO, PDE, O...
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...
Medical devices professional with more than 25 years' experience in senior management positions in early stage medical device companies. A...
Dr. Loleta R.
Seasoned clinician innovator (MD, MBA) and data-driven strategist with unique healthcare and business acumen. Proficient in leading in-depth ma...
I have 15 years of experience in the field of Public Health and Clinical Research in several positions: coordination, monitoring, project man...
• Experienced Clinical research professional, with the strong academic foundation of Graduation in Pharmacy and Post-graduation in Biochemical ...
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...
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...
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.
