Profile Summary
Dr. Alex L.
Qualifications: MBiochem Molecular and Cellular Biochemistry, Oxford University PhD Haematopoetic Stem Cell Gene Therapy, University of Manches...
Dr. Oyinkansola S.
Overview: As a dedicated Medical Doctor and accomplished Research Writer, I bring a unique blend of medical expertise and writing proficiency ...
Dr. Adam E.
My research interests are in the design, development and assessment of novel drugs to prevent brain injury in infants and adults.
Dr. Arinzechukwu U.
I have over 10+ years experience in medical/content/copywriting and proof-reading/editing as well as over 6+ years experience in cancer researc...
Dr. Murtaza Najabat A.
I am a biomedical engineer with over 20 years of experience in medical device development and healthcare technology. Apart from academia, I hav...
Dr. Pari J.
Digital Health an Medical/Scientific Affairs professional holding a Ph.D. degree in pharmacology with extensive academic and industry experienc...
Dr. Grace C.
1. Clinical Evaluation Report (CER) writer and authoring of Clinical Evaluation Plan (CEP) in accordance with Medical Device Regulation (MDR), ...
Dr. Loren D.
Loren DeVito, PhD, is a science and medical writer with expertise across a wide range of therapeutic areas, including oncology, neurology, card...
Dr. Geetanjali B.
I am a Ph.D. in Bioengineering with expertise in medical device development and innovation, experimental design, data analysis and interpretati...
Dr. Vera Bin San C.
Are you looking for a medical writer who can prepare regulatory submissions for an investigational medicinal product (IMP), e.g. clinical resea...
Dr. Manarshhjot S.
Product development specialist with multiple skills including data analytics, machine learning, CAD/CAM, prediction modelling. Specialist in de...
Dr. Waqar L.
Ten + years of hands-on technical working experience in the manufacturing environment covering Metal, Textiles, Food, Auto parts, Chemical proc...
Dr. Nitin M.
After completing MBBS from the All India Institute of Medical Sciences, New Delhi. He pursued MD in Radiodiagnosis from SMS Medical College and...
Dr. Krutika G.
Here you can find more info:https://www.krutikagohil.com/ I am an award-winning professional digital health innovator. With my well-founded s...
Dr. Muhammad Usman M.
I am an experienced and professional medical content writer, copywriter, article/blog writer, and a scientific researcher with a keen interest ...
Dr. Salma C.
- Ph.D. in immunology with 8+ years of experience in developing, conducting, and analyzing preclinical project.... - First author of three scientific publications....
Dr. Precious O.
I am experienced in
Dr. Alpa B.
I am Dr. Alpa Ben, a BDS graduate from India. I have been working with healthcare service industry from past 8 years and have experience in var...
Dr. Ankur P.
My expertise is development of clinical evaluation reports (CERs). This includes experience with literature searches, post-market surveillance,...
Dr. Surendra P.
I have 10 years experience in biomedical diagnostic devices development, biofertilizers, microbial enzyme fermentation technology, BMR, BPR, SO...
Dr. Nadeem A.
• Cell biologist with seven years of academic scientific writing experience • MBA candidate in Medical Devices and Healthcare Management with t...
Dr. Neeti S.
Ph.D. in Biotechnology with a biochemistry background and 6+ years of extensive research experience in academia. Microbiology, agriculture, pl...
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. Dr. Anu P.
WORKED AS A PROFESSOR,FULL TIME RESEARCH SCHOLAR
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...
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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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.
