Profile Summary
Dr. Shruthi E.
Career Objective: To secure a responsible career opportunity to adopt and utilize my public health knowledge and skills while making a signific...
Dr. Giri Nandagopal M.
I did my PhD in Microfluidics, where I worked on incorporating statistical and neural network techniques to generate key insights from complex ...
Executive Management |Project, Program, Portfolio Management - PMO ~ Robotics |Biotech | Pharma | Medical Devices | FDA I develop and delive...
Dr. Sahar R.
I am a professional medical writer and senior medical education specialist . I am highly skilled in medical communication and providing promoti...
Dr. Daniel P.
Trained Physician with clinical and 10+ years of practical experience in Market Access and Life Cycle Management of pharmaceutical products in ...
Dr. Bogdan M.
I am an PhD Chemical engineer with proven experience in quality assurance and regulatory affairs. Currently I am the J. Manager Global Regulato...
Dr. Sunday Ojochegbe O.
Dr. Okutachi is an experienced R and D Scientist in the highly regulated molecular diagnostics | IVD industry. He holds a PhD in Cancer Cell B...
Dr. Mohamed M.
Professional with scientific and business educational background, and more than 25 years diverse work experiences that covers the full value ch...
Dr. David M.
✔ Pharmacovigilance Physician, Medical Regulatory Writer, LQPPV, Project Manager, Clinical Trials Regulatory Expert. ✔13+ years professional me...
Dr. Nadeem A.
• Cell biologist with seven years of academic scientific writing experience • MBA candidate in Medical Devices and Healthcare Management with t...
Dr. Paula P.
- Degree in Pharmaceutical Sciences, Faculty of Pharmacy, University of Porto (2000) - PhD in Analytical Chemistry, Faculty of Pharmacy, Univer...
Dilip B.
Research personnel conducting safe and ethical human research with knowledge of federal regulation, research ethics and GCP guidelines. Skilled...
Dr. Brian W.
Ph.D. in chemistry (enzymology) with significant industrial experience in biocatalytic processes, in-vitro diagnostic, and medical device devel...
Dr. Tiffany Y.
Hi! I am a freelance medical writer who has written medical manuscripts and grants on a wide variety of topics, including medical devices, clin...
Dr. Augustin O.
Experienced researcher in advanced in vitro diagnostics and biomolecule production, with expertise in molecular biology, protein chemistry, mic...
Dr. Junaid Z.
This is Dr. Engr. Junaid Zafar. I have a PhD in Electrical & Computer Engineering from the University of Manchester, UK back in 2008. I ha...
Dr. Evita A.
A clinical research scientific writer with clinical medical, CSR. and regulatory CER expertise in MEDDEV 2.7/1 rev4 documentation, EU MDR and F...
Dr. Denali D.
I am a biomedical engineer and global health researcher specializing in female sexual and reproductive health. I have 10 years of R&D exper...
I am a scientist with a broad knowledge in biochemistry and medical related applications. I have experience in medical device development, and ...
Dr. Eric L.
With a strong scientific background, I bring extensive expertise in medical device development's regulatory and quality aspects. As an acco...
Dr. Fernanda A.
My name is Fernanda Aquino, and I am a highly qualified and dedicated professional with education and experience in both Brazil and the United ...
Dr. Jan I. Y.
I am a result-oriented, enthusiastic, experienced MD, Internist with a hematology background and good communication, proactive, and innovative ...
Dr. Srishti N.
"Research isn't complete until it has been communicated." A personal motto that has driven my passion for effective scientific c...
Dr. Eric G.
6 years of experience in consumer product development, medical device design and software engineering.
Dr. Karim E.
I hold a Ph.D. in Biological Sciences from the Université Libre de Bruxelles (ULB), Belgium, specializing in gene therapy against cancer. ...
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.
