Blogs
Facilitating the standardization of industry best practices
The Clinical Domain is Evolving. Make Sure your CTMS is Evolving with It.
The Evolving Role of CTMS in Risk Management takes a broad look at the challenges facing clinical trial management, how the clinical domain is changing, and how the industry can better respond.
ArisGlobal’s LifeSphere CTMS10 Brings Complete Control and Full Visibility to Clinical Trials
A versatile Clinical Trial Management Solution, LifeSphere® CTMS10 contains great functionality and five key benefits, addressing a variety of challenges in the clinical product lifecycle.
ArisGlobal’s LifeSphere MultiVigilance 10 Helps SMBs Manage and Master Pharmacovigilance
Managing and Mastering Pharmacovigilance covers how LifeSphere Multivigilance 10 benefits small to medium-sized businesses by utilizing industry-standard practices and proper management processes.
ArisGlobal’s LifeSphere Mobile Has Evolved into LifeSphere Reporter. Here is What That Means for You.
A key offering in ArisGlobal’s LifeSphere platform, LifeSphere Reporter empowers field reps, provides fields teams and approved users with secure access, and easily integrates with LSMV10 and other systems.
Presenting the All New Automation/Pharmacovigilance Knowledge Hub
ArisGlobal has created an Automation in Pharmacovigilance Knowledge Hub to help explain, in easily digestible terms, everything you need to know about automation in PV.
ArisGlobal Hosts Optimizing Adverse Event Reconciliation in Medical Affairs Webinar
Many life sciences companies are still utilizing a manual process for their medical affairs needs. ArisGlobal’s LifeSphere ® Medical Affairs platform can help automate this process. Learn more about Medical Affairs and automated processes with our webinar, Optimizing Adverse Event Reconciliation in Medical Affairs.
ArisGlobal Insights – Interview with Sandeep Mahagaonkar
This is the fourth in a four-part blog series that examines the Clinical, Medical Affairs, Regulatory, and Safety business units at ArisGlobal. Director of Product Management – Medical Affairs and Quality, Sandeep Mahagaonkar, spoke about what attracted him to ArisGlobal, the state of Medical Affairs, and the vision for 2020 and beyond.
ArisGlobal Insights – Interview with Pratyusha Pallavi
This is the third in a four-part blog series that examines the Clinical, Medical Affairs, Regulatory, and Safety business units at ArisGlobal. Senior Director, Regulatory Product Head at ArisGlobal, Pratyusha Pallavi, spoke of her role, the department vision, and product implementation
ArisGlobal Insights – Interview with Emmanuel Belabe
This is the second in a four-part blog series that examines the Clinical, Medical Affairs, Regulatory, and Safety business units at ArisGlobal. Associate Vice President of Product Management for the LifeSphere Safety portfolio, Emmanuel Belabe, spoke in depth about the vision for LifeSphere Safety for 2020 and beyond.
ArisGlobal Insights – Interview with Sondra Pepe
This is the first in a four-part blog series that examines the Clinical, Medical Affairs, Regulatory, and Safety product domains at ArisGlobal. Senior Director of Clinical Product Management, Sondra Pepe, describes what attracted her to ArisGlobal and articulated the vision for Clinical product strategy.