About this event
High-quality information is essential for pharmacovigilance teams to maintain accurate regulatory reporting, signal detection, and reliable analysis of patient safety.
But, the volume of safety data and documents arriving daily from disparate sources and partners is extensive, and the pressure to meet deadlines is intensifying due to more regulations and strict requirements. Plus, with a majority of Safety teams operating with labour-intensive processes and disjointed systems with limited support for interoperability, the data-quality challenges are only amplified.
Professionals working in Safety have to overcome :
In order to drive efficiency across Safety processes including PV Case Management, PSMF, SDEAs, Medical Inquiries and Risk Management, and enable better collaboration with Regulatory and Quality teams, professionals need the right tools to access properly structured data to easily create not only documents but full dossiers. There needs to be a cultural shift in the approach to managing safety from a data input view point to a process transformation standpoint.
Join us for this webinar to discover how a unified, data-driven platform for Safety can help your teams strike the balance between managing high quality content while simultaneously reducing the amount of time wasted. See how the CARA Life Sciences Platform pulls reliable information from any database across the organisation and collates it for use in Safety processes, reducing the time for tasks like the PSMF from ~100 hours, to just 5 minutes.
Our experts; Christian-Schmitz Moormann, Naomi Bradley, and Stefan Rupp, will provide insight in to how simplified data management and automations can drive efficiency and collaboration across Safety and its connected functions, saving valuable time and boosting efficiency.
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