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

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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…

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

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

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ArisGlobal Blogs

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

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ArisGlobal Blogs

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.

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ArisGlobal Blogs

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

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ArisGlobal Blogs

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

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ArisGlobal Blogs

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

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ArisGlobal Blogs

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 But too often, outdated clinical information management can make working…

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