Profile Summary
Dr. Dr. Anu P.
WORKED AS A PROFESSOR,FULL TIME RESEARCH SCHOLAR
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. Harsh V.
A competent pharma professional with experience in Scientific writing, Regulatory competitive intelligence, DRA, F&D, MSAT and QA. Experie...
Dr. Cynthia D.
Freelance Medical and Scientific Writer with 4+ years experience in scientific writing Science Blog Writer and Editor (biologicallycurious.com)...
Paul S.
I am a professional writer, copy editor, and medical editor with more than 10 years of writing and substantive editing experience. Since 2008,...
Denise A.
I am an experienced Quality and Regulatory professional with over 25 years in the medical device manufacturing industry. I have worked with Cla...
Selina B.
Medical Communications Consultant -Writing Clinical Evaluation Reports (CER) for medical device manufacturers -Preparation of clinical reports ...
Thariq A.
I am having experience in Medical writing, Regulatory affairs, Pharmacovigliance, i am able to do dossiers work, Licence work.
NAVEEN A.
Bio-pharma & Medical Device Quality Consultant having a good blend of Manufacturing, Technology & Business with in-dept...
Peggy G.
Having over 20-years’ experience working in nursing and public health research, I turned my focus to medical writing almost a decade ago. I ha...
Dr Febin F.
• Scientific Writer with experience in end-to-end handling of Clinical Evaluation Reports (CERs, both MDD and MDR compliance). • Authored scien...
Kavita S.
We are a team of experienced regulatory compliance expertise for Medical Devices and In-Vitro diagnostic devices across all risk classes. We ha...
Sachin M.
I am a medical device executive for last 20 years and have developed two innovative products, one nanotechnology based product among that. I ha...
Marysa M.
Marysa is a Medical Device Regulatory Consultant with over six years’ experience executing clinical-regulatory documentation and demonstrated k...
Lini S.
Specialities - Well-versed in EU Registration procedures (DC/MR, CP and nationals). - CMC Dossier Development & writing - Regulatory St...
Divya G.
NubGenix mainly focuses to support start up and mid-size medical device, combination products and pharmaceutical organizations. We provide supp...
Lakshman Prakash B.
Experience in Lifesciences industry including over 18 years’ experience in QA, QMS, Regulatory, Manufacturing, Quality Unit (Commissioning, Qua...
Tarun S.
Medical device professional with strong background in single use disposables, reusable medical devices(Class I, Class II and Class III) . Broad...
Shiva L.
Preparation of CER,PER, SSCP, PSURs, PMS Performing Literature search in Literature databases Hands on experience on Literature referencing to...
Mike K.
Mr. Khalil’s professional career spans over thirty (30) years of executive and entrepreneurial leadership in pharmaceutical, medical devices, n...
Vaibh K.
Medical device risk assessment
Jose A.
Behind every successful medical device registration, there is a team of experts working hard to ensure it meets regulatory requirements. As a Q...
Arjun L.
I have a blend of experience in clinical medicine, pharmaceutical industry and medical device industry....As a medical doctor, I work on infectious diseases, pulmonary and critical care and public health....
QUYNH N.
EDUCATION: - Master in Science, Technology and Health - Sorbonne Université - France - Clinical Research Associate Certificate EXPERIENC...
Anupam M.
Experience summary: Author and review regulatory periodic safety reports (Periodic Benefit-Risk Evaluation Reports Developmental Safety Updat...
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.
Keep your project private
Restrict who can see your project and send you proposals. Invite only specific freelancers to view your project.
NDAs and IP protection
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.
Contact experts directly
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.
Project Management
Keep track of files and conversations in the user-friendly Workspace.
Flexible, secure payments
You can choose to pay either a fixed or an hourly fee based on your requirement.
-
Looking for medical device writing expert$550.00
-
Hiring for medical device writing expert$500.00
Post your Project (Free)
Your project details are safe, secure and visible only to logged-in users.
Get Quotes & Choose Experts
Discuss your requirements in detail with the experts before accepting the final statement of work from Kolabtree.
Collaborate
Pre-pay for your project and work with the expert to get your desired output. Keep track of files and conversations in the user-friendly Workspace.
Job Done!
Approve the deliverables once you're satisfied with the job done.
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.
