Profile Summary
Dr. Amin H.
I’m a PhD-level Medical Writer and Biomedical Engineer with over 10 years of experience in clinical research, scientific writing, and regulator...
Karen A.
Hola, soy Karen, estudiante de Ingeniería en Biomedicina actualmente cursando el 7.º semestre de una carrera de 8 semestres. Durante ...
Lakshmi Rohini T.
Postgraduate in Microbiology from the Central University of Tamil Nadu with an advanced diploma in Clinical Research. I have hands-on research ...
Dr. Shifa J.
Regulatory Affairs and Scientific Research professional with 6+ years of combined experience in biotech, academia, and government. Skilled in r...
ALOKEPARNA C.
I help medical device startups, diagnostic innovators, and digital health companies build robust and compliant documentation aligned with ISO 1...
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Dr. Anushikha D.
I am a dentist and public health professional with a Master's in Public Health from All India Institute of Medical Sciences (AIIMS), Rishik...
Dr. Kandarp B.
I am a PhD in Microbiology with 17+ years of experience in scientific writing, editing, and research mentoring across life sciences and multidi...
Karissa T.
I’m a seasoned Regulatory Affairs Consultant with over 17 years of experience supporting medical device and IVD companies in achieving global c...
Dr. Peter R.
I am a research scientist with a PhD in biomedical engineering from Yale University with over 20 years of research experience, including conduc...
Dr. Ghali A.
PhD Mechanical Engineer specializing in inhalation/pharma process and equipment development. I help university labs, PI-led groups, and startup...
Dmitrii S.
I’m a computational biologist, ML engineer, and digital-health founder who turns life-science data into actionable insights and products. Wheth...
Dr. Luca M.
PhD in Biomedical Engineering with work and educational experiences in three countries (Italy, The Netherlands & US). Driven by a passion f...
Chittaranjan D.
Professionally certified consultant clinical specialist in radiology reporting with more than 22 years of experience. Extensive knowledge of im...
Dr. Harriet K.
Regulatory writing and submissions • Regulatory Intelligence and Strategy Development • Toxicology Study Monitoring • Due Diligence and Gap Ana...
Esther O.
I am an experienced Senior Research Nurse working within the NHS, with a strong clinical background in vascular nursing and accident & emer...
Dr. Sreerup B.
PhD in Biomechanics & Medical Image Analysis | MATLAB Expert | Translating Research into Medtech Innovation I am a PhD-qualified researche...
Ahmed Y.
I am a PhD researcher in Medical Microbiology with a Master's degree and three peer-reviewed publications in antimicrobial resistance and i...
Jarrell M.
I am a medical device professional with 25+ years of experience in R&D product development, risk management, and regulatory compliance. Thr...
Irina B.
QA compliance, Regulatory Affairs, FDA, MHRA, UKCA/ UK Conformity Assessment (for medical devices post-Brexit) HPRA, WDA, EU medical devices, p...
Dr. Bachir M.
Dr. Bachir Macuácua is a physician and public health specialist with over 15 years of experi...complex health data into compelling narratives for academic, policy, and public audiences....
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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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.