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
Removing the Squeeze on Clinical Operations through Transparency, Integration and Automation
Automation in Pharmacovigilance Data Processing – Do You Trust Artificial Intelligence?
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
Tomorrow’s Medical Information Tools Today
Medical affairs teams at the heart of Phase IV studies
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
The Big Picture in Safety, Part 4 of 4: Finding the Savings: A Whole-System Approach to Safety
The Big Picture in Safety, Part 3 of 4: Taking the Pain Out of Safety Data Management Leads to Better Quality
The Big Picture in Safety, Part 2 of 4: Simplicity + Automation = Productivity: The Pharmacovigilance Equation for Managing More with Less
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
A Look Back at Partnerships in Clinical Trials Europe
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
The Five Must-Haves in Automated SUSAR Distribution
The Challenge with Today’s Clinical Analytic Platforms
What You Need to Know About Upcoming EU Trial Transparency Exceptions
Integrated CTMS Is Vital to Today’s Clinical Trials
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