Blog

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.

With technical capabilities advancing and new solutions entering the market, clinical trial data management has been steadily evolving for years. But the COVID-19 pandemic has dramatically accelerated the shift towards automated data collection technologies. In this blog, we review this technological progression—and where the industry still needs to go.

When performing a data migration, validation and testing are imperative to minimize the risk of unplanned downtime, loss or data corruption. Here are 4 best practices to maintain integrity and compliance.