ArisGlobal Launches LifeSphere® MultiVigilance (LSMV) Platform Powered with Cognitive Computing


15th DIA Japan Annual Meeting 2018

November 11 – 13, 2018 | Tokyo, Japan


DIA 12th Annual European Medical Information and Communications Conference and Exhibition

November 14 – 15, 2018 | Vienna, Austria
Booth #14 | @Aris_Global

LifeSphere Platform

Clinical Development

Clinical Development provides solutions for clinical operations combined with clinical data management to offer the most complete clinical research platform in the industry.

Regulatory Affairs

Regulatory Affairs is a suite of next generation solutions for regulatory compliance that integrates compliance with business processes over the entire product management lifecycle.

PV & Safety

Pharmacovigilance & Risk Management offers a modern clinical safety and PV platform to improve compliance with global regulatory guidelines.

Medical Affairs

Medical Affairs platform offers a complete suite solutions for pre and post-marketing communications between internal and external stakeholders.


One of the key requirements of the new pharmacovigilance legislation (Regulation 726/2004) in the EU is simplified reporting of individual case safety reports (ICSRs) by a Marketin...

White Paper

On May 25, 2018 the long awaited Global Data Privacy Regulation (GDPR) was implemented. For breaking the law, companies will pay up to 4% of their global revenues or €20 million,...


Major regulatory reforms for drugs and medical devices are being initiated in China to ensure safe, innovative, effective and high-quality medicinal products are available to its p...

White Paper

In order to stay compliant with NMPA requirements (submitting all post-marketing ADRs in ICH E2B (R3) format), drug manufacturers are required to procure an electronic safety datab...