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Dr. Kurtulus G.
I am a freelance medical, scientific, and technical writer with high-quality researches at Harvard Medical School proven by research papers pub...
Dr. Aafaque K.
Welcome! I am Dr. Aafaque Khan, a seasoned scientist and dedicated researcher with a specialization in Biotechnology, Biochemistry, Genetic Eng...
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Denise A.
Hi, I'm Denise! I'm a Regulatory Affairs Professional with over 10 years of experience and a Master's Degree in Regulatory Affairs....
Nida A.
An experienced clinical research and medical device Technical file writer who has certified on MEDDEV 2.7/1 Rev#4 documentation, EU MDR 2017/74...
Madhu S.
Over 5 years’ experience in Quality and Regulatory Affairs, and technical submissions for a range of medical devices, including Orthopaedics, S...
Dr. Adam S.
Experienced scientific and medical writer with expertise in clinical writing (clinical trial protocol, CSR, IB, ICF) and regulatory writing (IN...
Dr. Dimitrios K.
I'm a Freelance Medical Writer and Consultant specialising in clinical trial materials, study publications, and competitive intelligence fo...
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...
Yasir K.
With over 8 years of technical content writing experience in a broad range of domains, I am a highly experienced Content Writer. My role involv...
Dr. Sophie L.
Ph.D. level scientist with more than 18 years of experience in both academia and industry. Experience in multinational corporations, managing d...
Dr. Ana Luiza C.
I have over 8 years of experience in Clinical Research, Regulatory Affairs and Quality Assurance of implantable and electro medical devices in ...
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Biomedical E.
I am Umair Ahmed, a seasoned Biomedical Engineer and Scientist offering over 7 years of comprehensive experience in the freelance medical devic...
Dr. Hrishikesh G.
Broad hands-on software and hardware development for medical devices such as diagnostic imaging devices (PET, MRI, X-Ray and Ultrasound), blood...
Dr. Tiago V.
BSc in Biology and a PhD in Life Sciences - Microbiology and Infection. I have > 10 years of experience of research in Infectious Dise...
Dr. SENTHILKUMAR S.
Scientific Writer with 10+ years of experience with a demonstrated history of working in the Medical Device domain, SME in Clinical Evaluations...
Dr. Archana N.
I am Scientific and Medical Writer with 12+ years experience in academic research and writing. I have a Ph.D. in Genetics from one of the top t...
Dr. Ahram Q.
My professional background is to technically write the Scientific content, assess the researcher in research work related to Bioinformatics and...
Sundeep A.
A seasoned professional with a decade of experience, I am a Leader and Speaker in the field of Quality Assurance & Regulatory Affairs, ...
Adam F.
I performed inspections and premarket approvals for FDA for 7.5 years. I am now a Senior Consultant operating out of Switzerland. I operate a...
Dr. Jeremy V.
I am a research scientist with 9+ years of experience designing, conducting and communicating research in biotechnology and medicine. I work as...
Stephane G.
R&D executive with a Masters in Plastics Engineering and 20 years of experience in the medical device industry; worked in both large-ca...
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Dr. Rahul S.
Co-Founder of RetroBioTech, a consulting firm providing CAP-CLIA assay validation, FDA filing services, Shandi Ingredients developing nutraceut...
Girish H.
An accomplished, versatile, results-oriented clinical research professional with over 16 years of experience in the Pharmaceuticals & M...
Rudra P.
We are a Contract Research Organization (CRO) that focuses on advanced project management, clinical operations, medical writing, statistical an...
Bharti S.
A strong background in virology, medical microbiology and public health qualifies me to work on COVID-19 projects (factsheets, COVID-19 at home...
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.
We take several measures to help you work with full confidence and peace of mind.
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Our T&C include a default confidentiality clause that protects your IP and NDA for added protection before disclosing project details.
Kolabtree ensures safety and security of your payments and personal information and project details. Kolabtree’s T&C includes a default confidentiality and NDA clause.
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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Speak directly with freelancers and explain your requirements.
100% satisfaction guaranteed
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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Keep track of files and conversations in the user-friendly Workspace.
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You can choose to pay either a fixed or an hourly fee based on your requirement.
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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.
