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FDA Regulation Breakdown – 21 CFR Part 820 – Subpart C Design Control – Section (E) Design Review
In today’s breakdown we’re going to focus on 21 CFR Part 820 – Subpart...
The Many Issues Life Science Training Departments Face Creating Online Training
It’s not easy creating engaging online training that adds value. We know because our...
We’ve Simplified ISO 13485:2016
Want to Become an Expert in ISO 13485:2016? Making it easy for your workforce...
Struggling to Get Your Workforce Excited about Compliance, Regulatory and GxP Training?
Do you find it challenging to get your workforce excited about compliance, regulatory and...
We’ve Simplified 21 CFR Part 820!
Want to Become an Expert in 21 CFR Part 820? Here’s why our program...
How to Create an ISO 13485:2016 Online Training Program in 5 minutes!
How to Create an ISO 13485:2016 Online Training Program in 5 minutes! [Recorded Webinar]...
User Roles Explained
User roles are vital as they provide each user with the appropriate level of...
9 Advantages Of Online Training in the Life Sciences
Online training is the art of knowledge transfer through the internet, from anywhere in...
Stop Rolling Out Boring Life Science Training!
Learnaboutgmp provides knowledge and expertise that empowers life science organizations globally to roll out...
[New] Custom Course Creation – Our Professional Services Team is Ready!
As our training platform continues to help companies manage compliance, optimize quality and elevate...