Document management is an important yet time-consuming process — especially if you’re not using an electronic system to help you. A computerized filing system can assist with creating, storing, ...

In pharmaceutical manufacturing, software validation is innovation’s silent killer. A single user requirements specification (URS) takes weeks. Test plans stretch for months. Change controls bog down ...

Learn how to build a Z-Rig, a mechanical advantage system designed for efficient pulling and hauling in rescue, off-road recovery, and rigging scenarios. This step-by-step tutorial demonstrates proper ...

Regulation and the pharmaceutical sector are intrinsically linked. Indeed, it’s no exaggeration to state that the global pharmaceutical sector is one of the most heavily regulated industries in the ...

Laboratories today face mounting pressure to maintain data integrity while navigating complex compliance requirements and evolving technologies. Despite advancements, many labs still rely on ...