Regulatory FDA medical device approval

$250-750 CAD

Closed

Posted

over 3 years ago

$250-750 CAD

Paid on delivery

Looking for a Certified Medical Device Regulatory consultant for the preparation of SW Documents for FDA. Experience with 510(k), medical device classification, 21CFR820, Quality Manual, Risk Management Procedure, Quality Procedure, Label for medical devices ser manual for medical devices IEC 62304 Medical Device Software ISO 13485 Quality Management System ISO 14971 Risk Management System

Technical Writing

Software Documentation

Research Writing

Software Architecture

Project ID: 27588391

About the project

3 proposals

Remote project

Active 4 yrs ago

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3 freelancers are bidding on average $477 CAD for this job

@errandssolution

Hi, My name is charity. I will provide you a quality technical report writing. I am a PhD writer with 8 years of experience in Research Writing, Software Architecture, Technical Writing and Software Documentation. I have worked on several similar projects of writing reports, and can deliver quality writing to tight deadlines. You can see an example of one of those projects in my portfolio here: https://www.freelancer.com/u/errands solution. Regards Charity

$555 CAD in 7 days

5.0

(10 reviews)

4.4

@SupremeWriters

Regulatory FDA medical device approval I have more than 7 years of writing experience, I am a master in writing. I can deliver your work according to your requirements, given deadline, and 0% of plagiarism. I have served more than 4000 clients in the past 7 years with 100% satisfaction. I assure you, I will provide you a masterpiece and you will like it for sure. Please visit my profile; https://freelancer.com/u/SupremeWriters Thank you

$250 CAD in 1 day