Hire a Medical Device Regulatory Writing Expert

Dr. Evita A.

Medical Writer/Regulatory Affairs/Project Manager
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USD 210/hr
Masters degree in Biomedical Science
United States

A clinical research scientific writer with clinical medical, CSR. and regulatory CER expertise in MEDDEV 2.7/1 rev4 documentation, EU MDR and F...

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USD 210/hr
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Dr. Cynthia D.

Freelance medical and scientific writer with an expertise in biotechnologies, molecular biology and rare diseases.
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USD 80/hr
Doctorate
France

Freelance Medical and Scientific Writer with 4+ years experience in scientific writing Science Blog Writer and Editor (biologicallycurious.com)...

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USD 80/hr
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Dr. Harsh V.

Medical/Scientific/Regulatory/Newsletter/CMC/Dossier/Research/Review/Thesis/Protocol/Report/Article writing & editin...
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USD 30/hr
PhD
India

A competent pharma professional with experience in Scientific writing, Regulatory competitive intelligence, DRA, F&D, MSAT and QA. Experie...

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USD 30/hr
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Denise A.

Medical Device Global Quality and Regulatory Expert
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Bachelor's of Science and Associates of Business Administration
United States

I am an experienced Quality and Regulatory professional with over 25 years in the medical device manufacturing industry. I have worked with Cla...

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Selina B.

Experienced medical writer
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USD 70/hr
Doctorate of Medicine (MD)
United States

Medical Communications Consultant -Writing Clinical Evaluation Reports (CER) for medical device manufacturers -Preparation of clinical reports ...

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USD 70/hr
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Thariq A.

Regulatory Affairs having 3+ experience in field.
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USD 20/hr
Master of Pharnmacy
India

I am having experience in Medical writing, Regulatory affairs, Pharmacovigliance, i am able to do dossiers work, Licence work.

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USD 20/hr
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NAVEEN A.

Pharmaceutical & Medical device professional
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USD 50/hr
Masters in Biotechnology
India

Bio-pharma & Medical Device Quality Consultant having a good blend of Manufacturing, Technology & Business with in-dept...

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USD 50/hr
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Peggy G.

Senior Medical Writer at Medtronic
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USD 95/hr
Medical and Scientific Writing
United States

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...

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USD 95/hr
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Dr Febin F.

Scientific Writer with 3+ year experience
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USD 50/hr
Doctor of Pharmacy
India

• Scientific Writer with experience in end-to-end handling of Clinical Evaluation Reports (CERs, both MDD and MDR compliance). • Authored scien...

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USD 50/hr
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Sachin M.

Medical Device Executive/ Medical Writer/CER Writer
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USD 100/hr
MS
India

I am a medical device executive for last 20 years and have developed two innovative products, one nanotechnology based product among that. I ha...

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USD 100/hr
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Kavita S.

Experienced Medical Device Regulatory Affairs professional
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USD 40/hr
Post Graduate Diploma in Management (PGDM)
India

We are a team of experienced regulatory compliance expertise for Medical Devices and In-Vitro diagnostic devices across all risk classes. We ha...

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USD 40/hr
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Marysa M.

Medical Devices - EU MDR SME - Clinical Eval and PMCF
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USD 200/hr
MSc. Regulatory Affairs
United States

Marysa is a Medical Device Regulatory Consultant with over six years’ experience executing clinical-regulatory documentation and demonstrated k...

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USD 200/hr
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Lini S.

Regulatory Affairs Expert with 20 Years Experience (Regulatory and Scientific Writing Services)
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USD 90/hr
MSc Pharmaceutical Chemistry
India

Specialities - Well-versed in EU Registration procedures (DC/MR, CP and nationals). - CMC Dossier Development & writing - Regulatory St...

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USD 90/hr
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Divya G.

NubGenix is a consulting organization who provide core solutions for your modern medical device and combination product
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Masters in Biomedical Engineering (Medical Device Commercialization Focus)
United States

NubGenix mainly focuses to support start up and mid-size medical device, combination products and pharmaceutical organizations. We provide supp...

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Lakshman Prakash B.

experience in Lifesciences in QA, QMS, Regulatory, EU-IVDR, medical device documentation writing clinical trial reports
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USD 100/hr
M.Sc Biochemistry
India

Experience in Lifesciences industry including over 18 years’ experience in QA, QMS, Regulatory, Manufacturing, Quality Unit (Commissioning, Qua...

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USD 100/hr
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Tarun S.

Clinical Evaluation Report preparation and review as per MEDDEV 2.7.1 Rev 4
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USD 60/hr
Masters in Biotech
India

Medical device professional with strong background in single use disposables, reusable medical devices(Class I, Class II and Class III) . Broad...

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USD 60/hr
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Vaibh K.

Toxicologist-Medical devices
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USD 10/hr
MS (Pharma)
India

Medical device risk assessment

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USD 10/hr
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Mike K.

FDA Regulatory Consultant
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USD 150/hr
Bachelor of chemistry and Biochemistry
United States

Mr. Khalil’s professional career spans over thirty (30) years of executive and entrepreneurial leadership in pharmaceutical, medical devices, n...

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USD 150/hr
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Shiva L.

Regulatory Medical writer with 6.5 years if experience
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USD 60/hr
Molecular Genetics and Molecular Biology
India

Preparation of CER,PER, SSCP, PSURs, PMS Performing Literature search in Literature databases Hands on experience on Literature referencing to...

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USD 60/hr
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Jose A.

Freelance Medical Device professional with over 25 years of experience implementing QMS systems and RA compliance
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USD 175/hr
M.S Clinical Nutrition
United States

Behind every successful medical device registration, there is a team of experts working hard to ensure it meets regulatory requirements. As a Q...

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USD 175/hr
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Arjun L.

Physician | Clinical & Medical Affairs | CER | Scientific Writing | Pharma labeling | Strategy | HealthTech ...
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USD 70/hr
Masters of Public Health (Epidemiology, Clinical Infectious Diseases and Global Health Majors)
India

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....

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USD 70/hr
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Alekhya A.

Scientific writer , Manuscripts case reports , Review of Literature , Content Writer
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USD 30/hr
MDS Periodontics
India

Iam having 5 years experience in Research Writing and also keenly interested to work in Clinical Evaluation Reports, PSU , SEO, SOP , Medical D...

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USD 30/hr
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QUYNH N.

Medical Writer - Medical Device Consultant - Clinical Evaluation Report - MDR/ Performance evaluation IVDR
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USD 150/hr
Master degree in Science, Technology and Health
Vietnam

EDUCATION: - Master in Science, Technology and Health - Sorbonne Université - France - Clinical Research Associate Certificate EXPERIENC...

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USD 150/hr
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Anupam M.

Clinical research postgraduate with more than 11 years of experience in Medical Writing & regulatory submission
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USD 20/hr
Bachelors, Chemistry
India

Experience summary:  Author and review regulatory periodic safety reports (Periodic Benefit-Risk Evaluation Reports Developmental Safety Updat...

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USD 20/hr
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Neethu A.

Medical Device Regulatory Specialist - U.S. FDA, 510(k), Specialized at Polymer glove 510(k) documentation
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USD 50/hr
Applied Electronics
India

Medical Device Regulatory Specialist with years of experience and a deep understanding of European and FDA medical device regulations. Investig...

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USD 50/hr
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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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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.