Blog

In this blog, we look at whether the Generis CARA Life Sciences Platform can be the all-in-one solution you need.

When you move to a new electronic trial master file (eTMF) system, leverage industry experience for a smooth process.

In this blog, we look at the Vault regulatory information management system to see whether it can be the solution for your regulatory needs.

Your electronic Trial Master File (eTMF) plays a critical role in life-changing research. We look at signs you need a new eTMF system.

Here are four warning signs your regulatory information management system may be fraught with mistakes and inefficiencies.

When we think of the future of any industry, it is nearly impossible to ignore the role artificial intelligence (AI) will play. Whether it is the future of healthcare, pharmaceuticals, or the entertainment industry, there are use cases for AI. Before we talk about AI in pharma, let’s look at how it is changing the…

Pharmacovigilance (PV) sits at the center of drug safety efforts. Here’s how a trusted pharmacovigilance technology partner can help.

To prevent data loss or corruption and minimize unplanned downtime and cost overruns, data migration testing is a crucial step.

CARA 5.3 is the next-generation life sciences content management platform from Generis. Here’s an overview of features that excite us most.