Data Quality in Pharmacovigilance

Data Quality in Pharmacovigilance
In today’s rapidly evolving pharmaceutical landscape, ensuring the safety and efficacy of drugs is more critical than ever—and pharmacovigilance plays a pivotal role in this mission. With the vast amount of data generated across the industry, maintaining high-quality information is essential for safeguarding patient health. However, common data challenges such as redundancy, inconsistencies, and gaps can disrupt pharmacovigilance workflows, delaying crucial safety decisions.
This must-attend webinar will dive into the importance of data quality in pharmacovigilance and offer practical solutions to tackle these challenges. Our expert speaker will provide insights into innovative strategies, including advanced data pipeline techniques that effectively detect and manage redundant or isolated data. You’ll also learn about best practices for optimizing data acquisition and integration, ensuring seamless pharmacovigilance operations.
We’ll explore real-world examples where deduplication and normalization techniques have been successfully applied to enhance data quality and streamline processes. Through case studies, you’ll see firsthand how efficient data management can dramatically improve the speed and accuracy of safety monitoring.
Finally, we’ll discuss the future of pharmacovigilance, with a focus on how emerging technologies like AI and machine learning are set to revolutionize data quality and integration, unlocking new opportunities to enhance pharmacovigilance operations.
Key Takeaways:
- The Importance of Data Quality: Understand how high-quality data is essential for pharmacovigilance and ensuring drug safety.
- Practical Solutions for Data Challenges: Learn actionable strategies to manage data redundancy, inconsistencies, and incomplete datasets using advanced techniques.
- Best Practices for Data Integration: Discover how deduplication, normalization, and seamless integration can enhance data consistency and workflow efficiency.
- Emerging Technologies: Explore how AI and machine learning are revolutionizing pharmacovigilance and driving improvements in data management.
- Real-World Recommendations: Gain expert advice on implementing effective data management practices that ensure better safety outcomes in pharma.
Join us to equip yourself with the latest knowledge and tools needed to enhance data quality in pharmacovigilance, ensuring better safety and efficacy of pharmaceutical products.
Speakers

Varsha Kishore
Product Management Leader, Maxis AI
Varsha Kishore Product Management Leader·Maxis AI Varsha Kishore is a strategic Product Management Leader at MaxisIT, where she spearheads the conceptualization and end-to-end delivery of flagship Agentic AI products. With over ten years of experience in clinical IT and Pharmaceutical industry, she has evolved from a high-impact Business Analyst into a visionary leader specializing in the integration of AI frameworks within GxP-compliant clinical trials. Varsha is recognized for orchestrating high-performing cross-functional teams to drive innovation and operational excellence.

Dr. Rachna Saralkar
Product Management Leader, Maxis AI
Dr. Rachna Saralkar is a double board-certified physician and Principal Investigator at Flourish Research, specializing in psychiatry, clinical informatics, and the application of AI in healthcare. She brings deep expertise at the intersection of clinical research, digital health, and emerging technologies, with a focus on advancing more efficient and patient-centered clinical development. Previously, she served as Medical Product Director at Deliberate AI, where she led the development of AI-enabled solutions for mental healthcare. She has also advised several early-stage health technology startups as a fractional Chief Medical Officer. Dr. Saralkar completed her psychiatry residency at Johns Hopkins University and holds a Master’s in Clinical Informatics Management from Stanford University School of Medicine.

