The Learn-WiseGo Blog

Medical device companies operating in the US and EU need training programs that satisfy two different regulatory frameworks at once: FDA expectations around quality system training in the US, and the EU Medical Device Regulation (MDR) training directive for companies selling into Europe. Meeting both means your training records need to be centralized, auditable, and consistent across every market you operate in — not maintained separately by region. What FDA expects from trai

Reports Data Sync Now Runs Every 2 Hours In order to optimize the performance and efficiency of Learn-WiseGo we changed the report data...

In the ever-evolving landscape of healthcare, patient safety stands as an unwavering cornerstone. Every year, healthcare professionals...

Implementing HTTP Strict Transport Security (HSTS) in Learn-wiseGo We are excited to announce that HSTS has been successfully implemented...

We’re excited to announce two new developments designed to give administrators more control and flexibility in managing their platforms.

New Features: Updates to Assignment Screen Logic Current System Logic As per the current assignment logic, when a Lesson Plan is...

New Features Lesson Plan expired Icon - We have introduced a new enhancement to the LP listing screen: the LP Expired icon. This feature...

In order to meet the new California standard (Senate Bill 553) we have updated our Introduction to Workplace Violence Course. These new...

Learn-WiseGo will have downtime for critical MS Azure Cloud service migration activities, which are part of our ongoing efforts to...

The Learn-WiseGo production build set for Thursday, July 18th will include the following: New Features: Add Emails and Export to Excel...