Profile Summary
Loughlin G.
I studied Microbology (H. BSc) in University College Cork (U.C.C) where I wrote a review article on the Applications of Phage Therapy as an alt...
Dr. Kanika S.
I am a PhD-trained medical writer copyeditor with over 4 years of experience. I hold a graduate-level certification in Medical writing and edit...
Morgan B.
Freelance writer with over 7 years in clinical research. I've been involved in medical device trials, drug trials, investigator-initiated s...
Anjali S.
Performance-driven professional with total 2 decades of rich & extensive experience in Clinical Research & Development, Pharmac...
Dr. Jasmien R.
Experience in craniofacial genetics, medical imaging on postdoctoral level. Experience in market research, intellectual property landscape and ...
Joshita M.
A passionate researcher, with a Master’s degree in Biomedical Engineering from Carnegie Mellon University (USA), I have 9 years of product deve...
Alifiya T.
I am a research scientist and medical writer trained in clinical trials research (MPH, Rutgers University, USA). I have experience working acro...
Dr. Thatiana Evilen d.
Graduated in Biological Sciences (Bachelor's degree) at São Camilo University Center (2008). Science Master’s degree (2012) and Ph.D. ...
Dr. Pranesh B.
Scientific Literature content review; editing, pre-publication refinement, curation, report authoring. Competitive intelligence; Technology pr...
Dr. JORDANA S.
Ph.D. in Pharmaceutical Sciences with solid expertise in preclinical research, chemical and biological safety, and toxicological evaluation. I ...
Dr. Sanjaya C.
I am a pro-active person trained in clinical pharmacology and biostatistics. Currently, I'm leveraging my clinician skills in the improveme...
Dr. Shilpee S.
I have many years of experience in biochemistry, molecular biology, and bioinformatics with an emphasis on enzymes and other metabolic proteins...
Dr. Dhaval P.
I am a PhD graduate with pharmacology specialization and have experience in handling clinical trial protocols, Clinical study reports, Manuscri...
Dr. Cameron R.
Currently working with multiple industry partners to incorporate NMR spectroscopy into their work flows. Partnerships are with consumer health,...
Dr. Brent R.
I own a consulting firm with over 70 years of experience throughout the entire lifecycle of pharmaceutical submissions. We ensure your Drug Sub...
Dr. Ana Carolina E.
PhD graduate with 6+ years of biomedical research experience in immunology, vascular biology and auto-immune diseases. Experience in phase III/...
Dr. Hani A.
I am a medical doctor (MBBCH) with a PhD in Molecular Pathology and a Master's degree in Biochemistry, bringing over a decade of experience...
Dr. Joyita B.
I am a materials scientist. I earned my masters and doctorate degree in materials science and engineering from the Indian Institute of Science,...
Dr. Trinadh Venkata Satish T.
Experienced Research Scientist with a Ph.D. and over 20+ years of demonstrated history of working in the areas of Tissue Engineering, Infectiou...
Dr. Natalie B.
• Solid knowledge of Good Clinical Practice guidelines, Medical Code of Conduct and local clinical trial regulatory requirements. • Medical an...
Dr. Paula d.
More than 17 years working as Health Care Consultant for different companies and agencies, as well as a professor from a private and public un...
Dr. Onkar S.
Medical Doctor & academician turned into pharmaceutical professional. +15 years of experience with leadership positions in drug develop...
Global professional, doctoral-level research experience in life sciences. Experienced in scientific writing, ICH-GCP E6 framework, clinical res...
Dr. Aissulu I.
CT: oncology, infections, gastro, gynecology, diabetes, CV; Public Health - policy, HTA, QA; Project Management in Regulatory submissions, CT, ...
Dr. Pharmanalytics S.
Having an experience of more than 15 years in the analytical and regulatory domain with sound technical understanding to fulfill different regu...
Kolabtree is the leading online marketplace for medical device regulatory writing experts. Post your project, get bids, and hire qualified medical device regulatory writing consultants quickly and easily.
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You will receive detailed proposals directly from Kolabtree. These proposals will include a comprehensive Statement of Work (SOW), project fees, milestones, and deadlines.
You can choose to pay either a fixed or an hourly fee based on your scope of work. Pre-pay for the next milestone. You have to approve the deliverables only if the quality meets your expectations. If you arn’t happy, we’ll refund your money.
Kolabtree will share multiple quotations for your project. You have the freedom to accept the quote that aligns with your project requirement and budget. You can get in touch with us in case you want to discuss the fee.
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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Looking for medical device writing expert$550.00
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Hiring for medical device writing expert$500.00
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Who Is a Medical Device Regulatory Writing Expert?
A medical device regulatory writing expert helps businesses create the necessary documentation required in order to obtain relevant accreditation to distribute medical devices into the market.
What Does a Medical Device Regulatory Writing Expert Do?
A medical device regulatory writing expert is primarily involved with creating various regulatory documents and dossiers that are required to be submitted by the applicant (in this case, the medical device manufacturer) to the concerned authorities for marketing authorization.
These documents are essential in order to attest that the product meets the mandates and laws laid down by the appropriate local and international regulatory bodies. This includes procedural documents, such as preclinical and clinical studies, as well as the approval documents.
Qualifications for a Medical Device Regulatory Writing Expert
Medical device regulatory writing experts typically hold a degree in the precise field they work in, such as medical or health science. In addition, they possess a strong knowledge of regulatory affairs, and a flair for writing.
In addition, medical device regulatory writing consultants have,
- Strong internship or hands-on training experience in the medical device industry
- Certifications from the likes of Regulatory Affairs Professional Society (RAPS), American Medical Writers Association (AMWA) etc
- Ability to keep themselves updates with the latest developments in the regulatory domain
- The writing skills required to document these rules in a clear and concise manner.
Benefits of Hiring Freelance Medical Device Regulatory Writing Consultants
With more medical writers and scientists offering their services on-demand, there is a great opportunity for businesses to outsource their regulatory consulting needs to freelance experts.
Freelance medical device regulatory writing experts typically charge less than full time hires, and can be collaborated with on flexible schedules. Freelance platforms usually have top medical device regulatory writers from across the globe, offering companies a chance to hire a consultant that is the right fit, without barriers such as location or paperwork.
Cost of Hiring a Medical Device Regulatory Writing Consultant
Freelance medical device regulatory writing consultants usually charge as low as $20/hour, all the way up to $175/hour, depending on expertise and experience. For projects that are more intricate and detailed, and require extensive research, writers may charge between $225-250/hour.
How to Post a Project to Hire a Medical Device Regulatory Writing Expert
Before posting a project to hire a freelance medical device regulatory writing expert, consider the following,
- Precise nature and scope of the regulatory approval and supporting documents required
- Length and budget of the project
- The niche expertise you’re looking for
Now, mentioning these details in the project description will help you narrow down your search, and find experts matching the precise criteria you’re looking for. On Kolabtree, you can scout and hire freelance medical device regulatory writing experts from across the globe within 24 hours.