Dr. Afsana S.
I'm Dr. Afsana Syed, Pharm.D having an overall experience of 3.5 years in Clinical Pharmacy (1 year) and medical writing (2.5 years). I'...
Dr. Rafaella P.
A research engineer with progressive experience across nanomaterials, hybrid materials, polymers, and composites, with knowledge in additive ma...
Dr. Maria Rosa M.
I am a PhD in Molecular and Cellular Biology and I have dedicated my career to the biomedical field of reproductive sciences, both at the clini...
Dr. Ashkan S.
I am a senior scientific researcher who has previously designed innovative products in MedTech and Water industry sectors. I have published/co-...
Dr. Anna T.
Biomedical engineer with 4+ years of experience in collaborative research (medical...imaging for nuclear medicine applications) and several years of strategic management of scientific publications...
Dr. Derek C.
I completed my PhD in Chemical Biology and have previously worked in the medical device, pharmaceutical, and in vitro diagnostics industries.
Dr. Mahmoud H.
Healthcare retail (pharmaceuticals and medical) business Development management Business planning Marketing planning Healthcare retail distr...
Dr. Harsh V.
A competent pharma professional with experience in Scientific writing, Regulatory competitive intelligence, DRA, F&D, MSAT and QA. Experie...
Madhoo P.
Life science researcher with over 15 years of full time work experience at research institutions, universities, and biopharma industries. Exper...
Mayuri B.
Attracting, engaging, converting, managing, and understanding your target customer is no child's play. However, the bumpy ride can be smoot...
Mark L.
Mark Luhovy, MD is a medical doctor and biomedical engineer who has dedicated 20 years to the pursuit of understanding the intersection of medi...
Dr. Andrew L.
Experience in medical writing and clinical management for pharma and medical device Fortune 500 companies, super specialty hospitals, and gove...
Selina B.
Medical Communications Consultant -Writing Clinical Evaluation Reports (CER) for medical device manufacturers -Preparation of clinical reports ...
Juan Manuel F.
Clinical Project Manager, Research and Development Technical Expert and University Lecturer. 9+ years in clinical research Studies: I have a b...
Sonali S.
Having experience in medical device regulatory affairs, EUMDR, USFDA 510K, ISO 14971, ISO 13485
Abimbola W.
I'm an experienced researcher and data analyst with over 10 years of experience in clinical research and data analysis using SPSS. I've...
Bina P.
Strong medical professional with experience in medical writing, clinical research, pharmaceutical drug research and article writing. Ability to...
shehryar h.
I m a Physiotherapist and Medical writer with 15 years clinical experience. I ever focus on creative innovations that really impact the lives.I...
Balaji C.
MDR and MDD Gap assessments and Remediation. Risk documents creation and all remediation process knowledge to get the CE mark for the product t...
NAVEEN A.
Bio-pharma & Medical Device Quality Consultant having a good blend of Manufacturing, Technology & Business with in-dept...
Jihan F.
I have 7 years of experience in the Diagnostic Imaging Equipment field as I have worked in Technoscan and Cairoscan radiology centres and Cairo...
Peggy G.
Having over 20-years’ experience working in nursing and public health research, I turned my focus to medical writing almost a decade ago. I ha...
AITZAZ r.
Always, Keen On, Keep Walking, Born to Win!
Madhu S.
• A competent Professional Medical Writer with over 7+ years' of experience in Regulatory Compliance, Quality Systems, Clinical Research, ...
Usman M.
Career Profile Regulatory Affairs Specialist with 5+ years of experience, in the creation and compilation of regulatory submissions to regulato...
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.