In this free webinar, learn about the challenges and approaches to safety data management and ICSR reporting. Attendees will learn how technology makes it easier to comply with global and regional requirements. The featured speaker will discuss the considerations for incorporating affiliates into one pharmacovigilance solution. Attendees will learn the strategies for adopting a single multilingual safety solution to meet country specific regulatory requirements.
TORONTO, Oct. 11, 2022 /PRNewswire-PRWeb/ -- Directly supporting multilingual case processing and regional regulatory requirements in a global pharmacovigilance solution, eliminates multiple reporting systems and provides a single trusted source of safety information. With real-time and unified data foundation, it is easier to track compliance and enable more timely reporting, submissions and distribution. In this webinar, the featured speaker will focus on managing ICSR reporting with improved pharmacovigilance solutions.
The traditional "hub and spoke" model for affiliate safety data management and reporting is inefficient with siloed information and lack of data standardization. Often, there are affiliate-specific workflows and multilingual intake and submission. Maintaining oversight and quality is challenging with a fragmented view, and impacts analysis and downstream requirements such as aggregate reporting.
Pharmacovigilance teams need agile processes for collecting and reporting data that can easily scale with increasing number of adverse events and evolving regulatory landscape. Allowing affiliates to process local cases in a global safety solution centralizes information and delivers greater oversight and monitoring for pharma companies.
Modern solutions are transforming safety with collaborative and streamlined processes by providing a flexible security model, greater accessibility to pharmacovigilance data and highly configurable workflows. Companies can manage the entire ICSR reporting lifecycle — with full visibility and traceability from collection to case submission, even when outsourcing and working with affiliates.
With real-time safety data, pharmacovigilance teams can improve compliance and perform timely benefit-risk evaluation and decision-making. Register to learn about reshaping global ICSR reporting to deliver real-time visibility and oversight.
Join David Kolosic, Senior Manager, Safety Strategy, Veeva Systems, for the live webinar on Tuesday, October 25, 2022, at 9am EDT (3pm CEST/EU-Central).
For more information, or to register for this event, visit Reshaping Global ICSR Reporting to Deliver Real-Time Visibility and Oversight.
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Contact:
Vera Kovacevic
Tel: +1 (416) 977-6555 x371
Email: [email protected]
Media Contact
Vera Kovacevic, Xtalks, +1 (416) 977-6555 x371, [email protected]
SOURCE Xtalks
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