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Architecting Atlassian for Healthcare and FDA Compliance: Part 1

Bridging the gap between agile development for innovation and audit readiness for compliance!
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Architecting Atlassian for Healthcare and FDA Compliance: Part 2

Using Atlassian’s Jira framework to transform and boost DevOps!
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6 Steps for Implementing a QMS Software

Learn the right steps to adopting an eQMS for your Medical Device or Life Science organization.
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What Atlassian's Elimination of Jira Server Means For Your Business

How the transition from Jira Server to Jira Cloud will impact Healthcare and Life Science Companies
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Using Agile in SaMD Development Under IEC 62304

Uncovering how Agile practices fulfill Software as a Medical Device (SaMD) Development
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What is FDA's 21 CFR Part 820?

Unpacking the FDA guidelines and regulations under 21 CFR Part 820.
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A Quick & Easy Guide to FDA Pre-Submissions

A simple guide to conquering your Pre-Submission Meeting with FDA, plus some free tools!
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Top 20 Medical Device Conferences to Attend in 2020

A simple breakdown of 20 conferences you don't want to miss this year.
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What is ISO 13485:2016?

An easily digestible overview of ISO 13485 and how it applies to your medical device company.
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ISO 13485 - Regulatory Requirements on Medical Devices

How embracing regulations can give you a leg up on your competition.
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