FDA 510K regulatory affairs

Closed Posted 3 years ago Paid on delivery

min $50 USD / hour

Closed

A startup medical device company is looking for a regulatory affairs specialist experienced in the cardiac diagnosis market space. The primary task requires extraction of the user requirements from the FDA 510K summary report. The user requirements will then be used in our product development plan life cycle. The second task is to establish substantial equivalency through comparison of our product specifications

The task applies to Class II B hardware devices and Software as Medical Device (SaMD) projects.

Medical

Project ID: #26412457

About the project

4 proposals Remote project Active 3 years ago

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4 freelancers are bidding on average $53/hour for this job

chraheelbhatti's Profile Picture
chraheelbhatti

I'm experienced research writer with 06 yrs of experience in the field. I have done multiple successful projects on this. I can help.

$50 USD / hour
(1 Review)
2.7
johnwanjiku's Profile Picture
johnwanjiku

Dear Prospective Client, Upon analyzing the assignment detailsFDA 510K regulatory affairs, I am assured that I will be capable to entire it diligently and professionally on the anticipated date. You are guaranteed; - I More

$50 USD / hour
(1 Review)
1.1
paigop's Profile Picture
paigop

I am a clinical researcher by profession for over 30+ years and worked in regulatory environments for both biopharmaceutical and medical device companies. I have recently done regulatory submission for a blutooth enabl More

$61 USD / hour
(0 Reviews)
0.0
Parastoosaberi94's Profile Picture
Parastoosaberi94

Hello, I'm a recent medical graduate currently catching my breath and working from home. I think I can live up to your expectations and look forward to hear from you. Thanks Parastoo

$50 USD / hour
(0 Reviews)
0.0
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