Profile Summary
A strong background in viorology, medical microbiology and public health qualifies me to work on COVID-19 projects (factsheets, COVID-19 at hom...
It's me Dr.Hamdan, professionally computational biologist. My profession, not only professionally, but my passion is to interact with globa...
Digital Health an Medical/Scientific Affairs professional holding a Ph.D. degree in pharmacology with extensive academic and industry experienc...
- Proven track record and accomplished projects and products for industrial SMEs and academic partners; - Multidisciplinary approaches using qu...
I am a scientist with a passion for marketing and business. I love to communicate dense technical and scientific knowledge in a clear, accessib...
1. Clinical Evaluation Report (CER) writer and authoring of Clinical Evaluation Plan (CEP) in accordance with Medical Device Regulation (MDR), ...
I am a freelancer with a Bachelor Degree in European Studies from De La Salle University and I am currently earning a postgraduate degree in Me...
Are you looking for a medical writer who can prepare regulatory submissions for an investigational medicinal product (IMP), e.g. clinical resea...
I have a Ph.D. in Immunology. I studied the negative regulation of immune responses, particularly on the role of the ubiquitin-modifying enzyme...
If you are an entrepreneur/founder in health-tech, I can help you * fine tune your strategy * navigate science, engineering, quality processes ...
Over 15 years of experience in the life sciences industry from R&D chemist, to drafting and prosecuting chemical, biochemical, and mate...
After completing MBBS from the All India Institute of Medical Sciences, New Delhi. He pursued MD in Radiodiagnosis from SMS Medical College and...
Ten + years of hands-on technical working experience in the manufacturing environment covering Metal, Textiles, Food, Auto parts, Chemical proc...
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Presently supporting EU MDR as Biocompatibility SME, Have experience in toxicology risk assessment of pharmaceuticals, cosmetics and medical de...
Here you can find more info:https://www.krutikagohil.com/ I am an award-winning professional digital health innovator. With my well-founded s...
Professor Mark Flynn is the Executive Director of Global Impact Cluster for Better Health Healthcare and Treatment at the University of Newcast...
Ph.D. in Electrical and Computer Engineering with concentrations in machine learning, statistical testing, and biomedical signal processing. Se...
Demonstrable track record for driving solutions to complex analytical problems. Possesses exceptional rigour in distilling and analysing data, ...
Medical Writer and Grant Writer for 7 years across innovation-intensive research organisations in Australia including the St Vincent’s Centre f...
Qualitative, ethnographic researcher in both academic and business contexts throughout Asia (Bangladesh, Cambodia, China, India, Japan) and Eur...
Market access for medical affairs, HEOR, payer facilitation, NICE/FDA implementation, budget impact modelling, HTA
I recently completed a PhD in medical engineering, involving: Correlative 3D imaging Biomechanics & Mechanobiology Medical device desig...
A competent pharma professional with +10 years of experience in Scientific and medical writings, Regulatory intelligence, DRA, F&D, MSAT, a...
As a scientist and an engineer, I have utilized my skill set to focus on multi-disciplinary problems. I have spent the last 8 years working clo...
My expertise is development of clinical evaluation reports (CERs). This includes experience with literature searches, post-market surveillance,...
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.
