Newscast: ArisGlobal Launches LifeSphere Clinical™
Removing the Squeeze on Clinical Operations through Transparency, Integration and Automation
Webinar Replay: The Evolving Role of the Medical Information
ArisGlobal Newscast: Industry’s Only E2BR3 Compliant Safety Multi-Tenant Cloud Platform
Connected to the Future: Making Safety Databases Transparent, Compliant and Cost-Effective
Automation in ICSR Processing – Is Artificial Intelligence the Paradigm Shift?
What to Look Forward to in Clinical Trial Innovations in 2017
Breaking Down Silos across the Life Sciences Enterprise Helps Drive Innovation
Removing the Pain Points from Overburdened Medical Affairs Teams
Enabling an Evidence-Based Approach to Pharmacovigilance and Safety
The Search for Simplicity, Scalability and Timely Insights in Regulatory Affairs
Automation in Pharmacovigilance Data Processing – Do You Trust Artificial Intelligence?
If You’re a CRO, You’ll Want to Read This Success Story
INFOGRAPHIC: Addressing Coding Challenges with a Centralized Medical Coding Tool
Webinar Replay: Recent Survey Reveals Compliance the Greatest Challenge for Drug Safety Teams
Drug Safety and Risk Management: Staying Current with Health Canada
Maintaining a Manual Approach to Drug Safety and Risk Management Puts Companies at Greater Risk of Scrutiny
Health Canada Puts Drug Safety Systems on the Map: The Ball is Now in Industry’s Court
Learn How Drug Safety Teams Can Overcome Resource Challenges
So You Have to Move off dsNavigator: How-to Advice on Switching Your Coding Tool
ArisGlobal Viewpoint: How Digitization Changes the Role of Regulatory Affairs
ArisGlobal Expert Shares How Regulatory Affairs Needs to Adapt to Transformation Change
Think Big: Regulatory Affairs Must Prepare to Respond to Strategic Business Drivers
A Secret Weapon to Act on Your IDMP Assessment
Regulatory Information Management: Solving the Compliance Challenge with a New Approach
Getting Ready for UDI: How Regulatory Information Management Simplifies Requirements for Medical Devices
Webinar Replay: Survey Reveals Many Regulatory Submissions Management Systems Are Not Future-Proofed
You Know Where The Regulatory Submissions Gaps Are – Do You Know How To Fix Them?
Five Key Steps You Need For Trial Disclosure
Promises, promises: Finding a CTMS that gives you what you need – Now!
A Look Back at Partnerships in Clinical Trials Europe
A level playing field: Realizing the importance of emerging CROs
CRO, R&D trends
Webinar Replay: Recent Poll Confirms Top Challenges of Contract Research Organizations – and What They Need from their CTMS
Becoming an Agile CRO with the ArisGlobal Pay-As-You-Grow Partner Program
Let me a tell you a clinical story………..
What is Really Required in a Modern EDC?
FDA Seeks Comments on the Use of Technologies in Clinical Research
Adverse Event Reporting Software Gets a New Friend: Mobile
New Rules Challenging Data Privacy Rentention Processes
Tomorrow’s Medical Information Tools Today
Medical affairs teams at the heart of Phase IV studies
Webinar Replay: Recent Survey Reveals Managing Multi-channel Communication Is the Greatest Challenge for Medical Information Teams
Leverage Our Medical Information Solutions to Solve Your Challenges
Learn the Five Keys to Success for Medical Information Service Delivery
Does your medical information software meet the latest in data privacy regulations?
Biotech Firm Transforms their Triage Process to Ensure Compliance, Reduce Risk