FDA Compliance for Patient Monitoring Software
Budget: $15 – $25 USD
I'm in the process of developing a comprehensive patient monitoring software designed to track and record heart rate, blood pressure, and glucose levels. The primary platform for this software is smartphones however we would like to apply as a standalone software as is can work with most of PPG based devices. Here's what I need assistance with:
- Navigating the complexities of FDA software as a medical device regulation/compliance
- Preparing necessary documents
Ideal applicants should have demonstrable experience in FDA regulation and compliance, particularly for software as a medical device. Insights in the software medical field, especially pertaining to patient monitoring, are crucial. Preferably, candidates should have undertaken similar projects in the past, and familiarity with software design for smartphones is a plus.
We use already prepared templates so there is no need to create documents from the scratch the main task will be to fill in those templates using a dedicated web-site for it.
- Navigating the complexities of FDA software as a medical device regulation/compliance
- Preparing necessary documents
Ideal applicants should have demonstrable experience in FDA regulation and compliance, particularly for software as a medical device. Insights in the software medical field, especially pertaining to patient monitoring, are crucial. Preferably, candidates should have undertaken similar projects in the past, and familiarity with software design for smartphones is a plus.
We use already prepared templates so there is no need to create documents from the scratch the main task will be to fill in those templates using a dedicated web-site for it.