LifeSphere product leaders share insight into how an effective IDMP strategy can support various business functions
MIAMI, FL and VIRTUAL, February 14, 2021 – ArisGlobal, the leading provider of life sciences software that automates core drug development functions with its end-to-end technology platform LifeSphere®, today announced two of its product leaders from its Regulatory segment will be presenting an on demand session at the 2022 DIA Regulatory Submissions, Information, and Document Management Forum (RSIDM) virtual and in person event.
Session Title: Beyond Regulatory Information Management: Leveraging IDMP Across All Business Functions to Proactively Manage Global Regulatory Affairs
Session Date/Time: On Demand, Monday, February 14 – Wednesday, February 16, 2022
Sonia Hurley, Sr. Director, Product Management, Regulatory
Robin Schilling, IDMP Product Manager
Sonia Hurley, Sr. Director, Product Management, Regulatory, is a seasoned regulatory professional with over 20 years of experience with highly regulated products in the Biotech/Life Sciences arena.
Robin Schilling, IDMP Product Manager, brings a diverse portfolio of 20 years of experience across government, military intelligence and life sciences. She is the product lead supporting the development and updates to LifeSphere IDMP.
LifeSphere IDMP has been recognized by industry analysts Gens & Associates as the most-ready IDMP software available.
At DIA’s Regulatory Submissions, Information, and Document Management (RSIDM) Forum, attendees will hear from industry and regulatory stakeholders working across the scope of regulatory information to examine current and evolving data standards and requirements and effective regulatory information management approaches to align related systems.