Skip to content

ArisGlobal Blogs

Categories
Look at paperwork and regulations

Nothing evolves within a vacuum. While today we can transmit reports, research, and more at the click of…

Learn More

What will the next generation of reporting and analytics in pharmacovigilance be? Will it move the needle on business innovation…

Learn More

Managing a clinical trial is no small feat. Documents must be tracked, client sites monitored, notes and findings to…

Learn More

The Future of Drug Safety Intelligence The future of safety intelligence is closer…

Learn More

ArisGlobal Announces the…

Learn More

Every person who wants to participate in clinical research should have the opportunity to do so…

Learn More
hands typing on

There’s no doubt that the pharmaceutical industry is well into its ‘age of automation’. A…

Learn More
looking at slide under microscope

Managing your Trial Master File (TMF) is a necessary, and often tedious task for most clinical stakeholders—but it doesn’t…

Learn More
doctor discussing test results

Identification of Medical Products (IDMP) has been harmonizing data globally across the drug development lifecycle since 2003. At its…

Learn More

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

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