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We design customized, innovative, and cost-efficient processes for clinical safety, pharmacovigilance, and medical affairs. Our deep industry knowledge and up to date insights let us combine agile, people-powered intelligence with big data in pioneering customer-centric solutions.
Discover the nuances of multilingual intake, local literature search, and local PV responsible/safety officer implementation with our expert-led webinar on: EU PV Optimization: Streamlined Technology Driven Oversight & Unified Governance
Don’t miss out! Register now @ https://bit.ly/Webinar-EuPv
03/13/2024
Join our experts Dr. Sumit Verma and Dr. Parul Singla for an in-depth exploration of EU PV Optimization: Streamlined Technology Driven Oversight & Unified Governance on 4th April.
Key takeaways:
• Comprehensive Understanding of Local Responsible Person (LRP) Requirements: Participants will gain insights into the landscape of LRP requirements in the EU.
• Importance of local literature searches in pharmacovigilance within the EU.
• Practical strategies for handling the complexities of multi-language adverse event (AE), product quality complaints (PQC), and medical information intake for drugs and devices in the EU.
• Explore methods for seamless integration with the central QPPV office, emphasizing on centralized operations management and governance, along with leveraging technologies to optimize overall pharmacovigilance processes.
Don't miss this opportunity to gain valuable knowledge and optimize your EU PV practices. Register @ https://bit.ly/Webinar-EuPv
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