Blogs

Practical Use Cases of Automation in Pharmacovigilance and Regulatory E-2-E Productivity: Part 2 of 2: How Far Along the Road Are You in Realizing Benefits from Automation in Safety? In Your Organization, Which Areas Would Create Maximum Value?

Practical Use Cases of Automation in Pharmacovigilance and Regulatory E-2-E Productivity – Part 1 of 2: What Is Your Greatest Challenge Across the E-2-E Process? How Would You Rate Your Automation Capabilities?

Protecting Data Privacy with Automation Is a Critical Step as GDPR Set to Become Law

Extracting Safety Signals from Social Media through Artificial Intelligence

Lifting the Tedium of Medical Literature Monitoring with Automation

The Push-Pull of Artificial Intelligence in Pharmacovigilance

National Pharmacovigilance Systems Part 3: Advanced Pharmacovigilance Technologies – A Solution for Deficiencies

National Pharmacovigilance Systems Part 2: Modern Technologies in Pharmacovigilance- The Way Forward

National Pharmacovigilance Systems Part 1: Pharmacovigilence with an ‘e’

Automation in Pharmacovigilance Data Processing – Do You Trust Artificial Intelligence?

Taking a Best Practices Approach to Safety Signal Detection and Risk Management

Signal Detection & eRMR: New EudraVigilance System Is Almost Here – Are You Ready?

Practical Use Cases of Automation in Pharmacovigilance and Regulatory E-2-E Productivity: Part 2 of 2: How Far Along the Road Are You in Realizing Benefits from Automation in Safety? In Your Organization, Which Areas Would Create Maximum Value?

Is Regulatory Affairs Ready for Automation? Part 3: Rating Your Organization’s Regulatory Data Science Capabilities

Is Regulatory Affairs Ready for Automation? Part 2: Are you Ready for a ‘New’ Technological Revolution?

Is Regulatory Affairs Ready for Automation? Part 1: What Is Your Greatest Regulatory Challenge?

The Search for Simplicity, Scalability and Timely Insights in Regulatory Affairs

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

You Know Where The Regulatory Submissions Gaps Are – Do You Know How To Fix Them?

Survey Finds Slow But Steady Move toward a Unified Clinical Platform

Removing the Squeeze on Clinical Operations through Transparency, Integration and Automation

What to Look Forward to in Clinical Trial Innovations in 2017

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

So You Have to Move off dsNavigator: How-to Advice on Switching Your Coding Tool

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

Medical Information: Easy Integration of LifeSphere MI with Your Chosen CRM Lets You Have Your Cake and Eat It Too

Mobility and Medical Affairs: Enabling Communication and Collaboration – Technology Considerations – Part 2

Mobility and Medical Affairs: Enabling Communication and Collaboration across the Stakeholder Spectrum – Part 1

Removing the Pain Points from Overburdened Medical Affairs Teams

Adverse Event Reporting Software Gets a New Friend: Mobile

New Rules Challenging Data Privacy Retention Processes

Tomorrow’s Medical Information Tools Today

Medical affairs teams at the heart of Phase IV studies

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

Webinar Replay: The Evolving Role of the Medical Information Professional

Newscast: LifeSphere Regulatory™ – Unified Cognitive Platform for Regulatory Affairs & Compliance

Newscast: Regulatory 2025: Developing an effective 10-year strategy for technology-enabled regulatory transformation

Newscast: LifeSphere Mobile MA™ – Self Service Medical Information Portal for Medical Affairs and Pharmacovigilance

Newscast: LifeSphere Intake and Triage

Newscast: ArisGlobal Launches LifeSphere Clinical™

ArisGlobal Newscast: Industry’s Only E2B R3 Compliant Safety Multi-Tenant Cloud Platform