November 27, 2019
Here’s Everything You Need to Know About USP 797 Guidelines
Recently, the USP-NF announced it was postponing some updates, including changes for USP 797. The updates were supposed to take effect on December 1, 2019. Many pharmacy personnel were wondering what changes they’d need to make. What do the current USP 797 guidelines say about compounding environments anyway? If you have questions, this guide has the
Read More
March 18, 2019
BIMO Inspection Readiness Checklist & Guide: FDA BioResearch Monitoring of Clinical Trials
Did you know that an FDA inspector typically schedules a bioresearch monitoring (BIMO) audit within five days of arrival? Would your clinical have BIMO inspection readiness in such a short time? Well, it should be: these inspections can occur at any time during a clinical trial, and there is no hard rule for how much notice they have to provide. If you are
Read More
February 15, 2019
Smart Lab: How IoT Healthcare Devices Will Improve Medical Research Labs
The “Internet of Things” has been growing at a stunning rate. Some experts have estimated more than 20 billion devices will be connected by 2020. There are already more devices connected to the IoT than there are people on the planet. The sheer expansiveness of the IoT has meant no field has been left untouched. Healthcare is
Read More
November 16, 2018
How a CO2 Monitor Can Ensure Your Lab is Safe and FDA Compliant
Having high levels of carbon dioxide (CO2) in your laboratory can be potentially life-threatening for your employees if the proper precautions aren’t taken. Monitoring CO2 levels in your lab is essential in ensuring the quality of your product while maintaining FDA compliance. Fortunately, CO2 monitors are designed to keep your technicians and products safe. If you aren’t sure what
Read More