Skip to content

Blog

Categories

Why Having a Well-Prepared eTMF is Important A well-prepared Electronic Trial Master File (eTMF) is critical to the success of…

Learn More

Your team’s workload grows by the day. The volume of Safety cases you’re managing increases significantly every year. All the same, the internal pressure to…

Learn More

Regulatory teams serve as the common thread of pharmaceutical research and development, connecting each domain on a drug’s journey to approval. Theirs…

Learn More

When saddled with legacy medical information systems, Medical Affairs teams are forced to behave like detectives, hunting down information…

Learn More

The coronavirus pandemic ushered in a new era of public scrutiny for the pharmaceutical industry. The general population was…

Learn More

Learn why Breakthrough is more than just an event but a summit for thought leaders in health and life sciences to discuss today and the future.

Learn More

Contract Research Organizations (CROs) have been enthusiastic early adopters of the LifeSphere electronic Trial Master File…

Learn More

It’s hard to think about COVID-19 and vaccine production, without reflecting on the speed, safety, and risks involved…

Learn More

As the pharmaceutical industry adapts to a new world with a new set of challenges, it is critical to keep…

Learn More

Collaboration is at the heart of most medical breakthroughs. But too often, outdated clinical information management can make working…

Learn More
White Paper: The Evolution of Signal Detection and Management   View More