Blog

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

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…

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

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

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

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.

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

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

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

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 But too often, outdated clinical information management can make working…