Hire a Medical Device Regulatory Writing Expert

Dr. Adam S.

Scientist and medical writer with experience writing clinical and regulatory documents, publications,
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USD 100/hr
PhD
United States

Experienced scientific and medical writer with expertise in clinical writing (clinical trial protocol, CSR, IB, ICF) and regulatory writing (IN...

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USD 100/hr
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Bharti S.

Scientific & Medical writer, COVID-19 virologist, Journal manuscript writing, Editor, Research papers, clinical tria...
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USD 102/hr
Master of Public Health (M.P.H.), Fundamentals of Clinical Trials
India

A strong background in virology, medical microbiology and public health qualifies me to work on COVID-19 projects (factsheets, COVID-19 at home...

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USD 102/hr
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Dr. Alex L.

Former academic, medical devices regulatory affairs consultant, specialising in clinical and performance evaluation.
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Doctor of Philosophy (PhD) Haematopoetic Stem Cell Gene Therapy
United Kingdom

Qualifications: MBiochem Molecular and Cellular Biochemistry, Oxford University PhD Haematopoetic Stem Cell Gene Therapy, University of Manches...

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Dr. Oyinkansola S.

Medical Doctor and Writer: Bridging Knowledge and Communication in Healthcare
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USD 40/hr
MPH
United Kingdom

Overview: As a dedicated Medical Doctor and accomplished Research Writer, I bring a unique blend of medical expertise and writing proficiency ...

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USD 40/hr
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Dr. Adam E.

Freelance drug and medical device Regulatory Affairs consultant | Expert in preclinical and clinical trial design
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USD 100/hr
Doctorate of Philosophy (PhD)
Australia

My research interests are in the design, development and assessment of novel drugs to prevent brain injury in infants and adults.

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USD 100/hr
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Dr. Arinzechukwu U.

Freelance Scientific Writer and Consultant with over 6+ years in cancer research
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USD 100/hr
Molecular Haematology
United Kingdom

I have over 10+ years experience in medical/content/copywriting and proof-reading/editing as well as over 6+ years experience in cancer researc...

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USD 100/hr
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Dr. Murtaza Najabat A.

Medical Device Development | Healthcare Technology Specialist | Regulatory Affairs Specialist
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USD 80/hr
PhD in Materials Science
Pakistan

I am a biomedical engineer with over 20 years of experience in medical device development and healthcare technology. Apart from academia, I hav...

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USD 80/hr
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Dr. Pari J.

Medical Advisor/Clinical Research professional with PhD and 10+ years of global experience in Healthcare Industry
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USD 90/hr
PhD - Pharmacology
Australia

Digital Health an Medical/Scientific Affairs professional holding a Ph.D. degree in pharmacology with extensive academic and industry experienc...

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USD 90/hr
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Dr. Grace C.

Experienced CER Writer for medical device companies
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USD 50/hr
Doctor of Philosophy (PhD) in Molecular Medicine
Malaysia

1. Clinical Evaluation Report (CER) writer and authoring of Clinical Evaluation Plan (CEP) in accordance with Medical Device Regulation (MDR), ...

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USD 50/hr
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Dr. Geetanjali B.

Research Scientist with experience in Medical Devices, Pre-clinical Research and Writing
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USD 50/hr
PhD
United States

I am a Ph.D. in Bioengineering with expertise in medical device development and innovation, experimental design, data analysis and interpretati...

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USD 50/hr
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Dr. Manarshhjot S.

Freelance development engineer. Specialist in prediction modelling, medical devices and medical data analytics.
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USD 30/hr
ME
United States

Product development specialist with multiple skills including data analytics, machine learning, CAD/CAM, prediction modelling. Specialist in de...

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USD 30/hr
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Dr. Vera Bin San C.

Regulatory Medical Writer with 10+ year of Scientific Publication Experience | Eye on Biostatistics Det...
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USD 90/hr
PhD
France

Are you looking for a medical writer who can prepare regulatory submissions for an investigational medicinal product (IMP), e.g. clinical resea...

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USD 90/hr
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Dr. Waqar L.

Auditing, Consulting, Training and Operations Management for International Standards i.e. ISO, BSCI, DIN, MDD, MDR, PPE
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USD 75/hr
PhD
Pakistan

Ten + years of hands-on technical working experience in the manufacturing environment covering Metal, Textiles, Food, Auto parts, Chemical proc...

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USD 75/hr
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Dr. Nitin M.

Scientific Advisor at Melior Life Sciences (CRO) | Consultant Radiologist | AI Research Advisor at Synapsica |
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USD 125/hr
MD
India

After completing MBBS from the All India Institute of Medical Sciences, New Delhi. He pursued MD in Radiodiagnosis from SMS Medical College and...

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USD 125/hr
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Dr. Muhammad Usman M.

Medical content and copywriter
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USD 15/hr
Medical Writing
Pakistan

I am an experienced and professional medical content writer, copywriter, article/blog writer, and a scientific researcher with a keen interest ...

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USD 15/hr
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Dr. Krutika G.

CMedO| Medical Device Expert | 10+ years of experience in healthcare with clinical and usability research
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USD 200/hr
PhD Neurophysiology (Emphasis Psychology)
Germany

Here you can find more info:https://www.krutikagohil.com/ I am an award-winning professional digital health innovator. With my well-founded s...

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USD 200/hr
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Dr. Salma C.

Ph.D, Clinical Reseach Professional
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USD 40/hr
PhD
Canada

- Ph.D. in immunology with 8+ years of experience in developing, conducting, and analyzing preclinical project.... - First author of three scientific publications....

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USD 40/hr
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Dr. Precious O.

Freelance Medical Writer with 5 year experience in Biomedical/Clinical Research
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USD 25/hr
Medical Degree (MD)
Nigeria

I am experienced in

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USD 25/hr
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Dr. Alpa B.

Medical writer with 8+ years of experience in writing CEPs, CERs, PMSRs and SSCP for Class II Medical Devices
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USD 30/hr
Bachelor of Dental Surgery
India

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...

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USD 30/hr
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Dr. Ankur P.

Experienced CER Writer
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USD 85/hr
Master of Science
United States

My expertise is development of clinical evaluation reports (CERs). This includes experience with literature searches, post-market surveillance,...

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USD 85/hr
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Dr. Surendra P.

Medical Diagnostic devices based on molecular, immuno platform, Fermentationn technology, biofertilizers, BMR BPR SOP
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USD 30/hr
PhD
India

I have 10 years experience in biomedical diagnostic devices development, biofertilizers, microbial enzyme fermentation technology, BMR, BPR, SO...

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USD 30/hr
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Dr. Neeti S.

Ph.D. Biotechnology, Experienced Research Professional.
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USD 50/hr
PhD Biotechnology
Germany

Ph.D. in Biotechnology with a biochemistry background and 6+ years of extensive research experience in academia. Microbiology, agriculture, pl...

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USD 50/hr
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Dr. Nadeem A.

Cell and Molecular Biologist | MBA in Medical devices and Healthcare Management | Certified in Regulatory Affairs - GxP
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USD 80/hr
The London School of Economics and Political Science (LSE)
Germany

• Cell biologist with seven years of academic scientific writing experience • MBA candidate in Medical Devices and Healthcare Management with t...

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USD 80/hr
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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. Dr. Anu P.

Scientific writer,editor with 6+ years of experience in image,video,and medical signal processing. paper reviewer
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USD 75/hr
PhD
India

WORKED AS A PROFESSOR,FULL TIME RESEARCH SCHOLAR

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USD 75/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.