In this free webinar, learn how interconnected regulatory data can enable every aspect of life sciences and inform strategic decisions. Attendees will gain insights into the role of automation in creating efficiencies and reducing costs for regulatory affairs and operations. The featured speakers will discuss regulatory’s connection to pharmacovigilance and its role in improving patient safety through global product data standards.

TORONTO, April 25, 2023 /PRNewswire-PRWeb/ — Life sciences companies face mounting internal pressures such as inflation, sourcing and manufacturing uncertainty and ever evolving global regulations. Additionally, internal pressures are calling for teams to operate lean and leverage data to solve problems. Together, these external and internal forces present a new wave of challenges for regulatory affairs and operations professionals, especially when managing a sprawling, global product portfolio.

Fortunately, the rapid pace of technology innovation and emerging global data standards provide industry with a new toolset that can be harnessed to bring drugs to market safely and efficiently while achieving commercial success. Life sciences companies can leverage advanced technologies like artificial intelligence (AI) to reduce manual effort and save time by shifting functions like ingestion and tracking of health authority correspondence from mostly manual to automated. Global data standards like ISO Identification of Medicinal Products (IDMP) and HL7’s Fast Healthcare Interoperability Resources (FHIR) promote quick and efficient exchange of information. Interoperability between systems and regions of the world has great potential to lower the cost of operations and create meaningful connections between functional areas such as regulatory and pharmacovigilance.

Join this webinar as ArisGlobal regulatory leaders highlight the potential of intelligent automation and interconnected regulatory data to inform strategic decisions and other key strategies for proactive management of a global product portfolio. They’ll also share use cases and practical steps that regulatory leaders in life sciences can take to ride the next wave of innovation in technology and global data standards.

Join Laura Jones, Director, Regulatory Product Management, ArisGlobal; Robin Schilling, Associate Director, Regulatory Product Management, ArisGlobal; and Renato Rjavec, Director of Products, Amplexor Life Sciences, for the live webinar on Friday, May 12, 2023, at 11am EDT (4pm BST/UK).

For more information, or to register for this event, visit Global Product Management: Navigating Regulatory Pressures with Automation & Interconnected Data.

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Contact:
Vera Kovacevic
Tel: +1 (416) 977-6555 x371
Email: vkovacevic@xtalks.com

Media Contact

Vera Kovacevic, Xtalks, +1 (416) 977-6555 x371, vkovacevic@xtalks.com

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