Felix Arellano
Global Head of Drug Safety – Roche

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Hans van Leeuwen
Global Head Regulatory Operations – Astellas

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Julie Thomas
Vice President, Global Medical Safety Operations – J & J

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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?

What is the greatest challenge across end-to-end pharma processes? How would you rate your automation capabilities? This two-part blog series analyzes attendee polling responses from a recent DIA webinar and shares ArisGlobal’s thinking about practical use cases for automation in pharmacovigilance and regulatory.

Moving to Self-Service: A Key Component of an Effective Automated Content Management Strategy for Medical Information Managers

By 2020, 67% of physicians will be digital natives and will prefer obtaining medical information on specific medications through digital channels, and by 2025, 75% of our global workforce will be accomplished by millennials who are extremely comfortable with digital technology. In this final blog of our two-part series, we share how the move to self-service is creating a clear paradigm shift and impacting the content management strategy of today’s MI departments.

ArisGlobal is a pivotal partner in the life sciences industry, specializing in solutions that drive drug development, safety monitoring, and regulatory compliance. We collaborate with more than 500 global life sciences companies, CROs, and government health authorities, including leading biopharmaceutical firms and regulatory bodies such as FDA, Health Canada, and NMPA.
Headquartered in the United States, ArisGlobal has regional offices in Europe, India, Japan and China.

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