Artificial intelligence (AI) is poised to have a transformative impact across the entire drug development continuum from preclinical research to post-marketing support.
When implemented appropriately, AI-driven technologies, from natural language processing and predictive analytics to machine learning algorithms, can streamline workflows, enhance signal detection and improve risk management. The key to effectively harnessing AI in life sciences is understanding the obstacles to be overcome and how technology can be used to mitigate those challenges.
Pharmacovigilance (PV) is an area of drug development that is prime for AI transformation. Confronted with an increasing volume and velocity of data that must be sourced from diverse channels, case processors are challenged to maintain accuracy, speed and regulatory compliance. Leveraging AI as an enabler to optimize the aspects of PV that are onerous streamlines intake and tracking, reserving human resources for the work that requires human intervention.
This webinar will explore the effective use of AI across the clinical development–post-marketing continuum, with a focus on how process automation and tech-enabled innovation is reshaping the landscape of PV. The key topics will include:
- Current trends in AI for drug development
- Challenges of PV
- AI solutions for streamlining post-market safety monitoring
- Future opportunities for AI in the clinical development–post-marketing continuum
Register for this webinar to stay ahead of AI advancements in life sciences and learn how to integrate innovative solutions into drug development strategies.
Speaker

Anna Russo, VP Machine Learning and Artificial Intelligence, Ergomed
With over 15 years of experience in Data Science and Artificial Intelligence, Anna brings a wealth of expertise and a track record of innovation. Her diverse career spans industries including healthcare, luxury, travel, and media, where she has successfully led AI-driven initiatives that enhance decision-making and operational efficiency.
In her current role, Anna is responsible for leading Data, AI, and ML strategy. She focuses on optimizing processes, delivering actionable insights, and driving innovation across clinical trials and pharmacovigilance. Her leadership and deep expertise advance global healthcare through transformative, cutting-edge solutions.
Who Should Attend?
This webinar will appeal to those working in the following areas or having the following job titles:
- Pharmaceutical, biotech and medical device professionals involved in clinical development and pharmacovigilance
- Regulatory affairs and compliance specialists
- Drug safety and risk management teams
- AI and digital transformation leaders in life sciences
- Healthcare data analysts and technology innovators
- Anyone interested in leveraging AI for drug development and patient safety
What You Will Learn
Attendees will learn about:
- How AI is transforming drug development from early research to post-marketing surveillance
- The role of AI in optimizing pharmacovigilance, improving accuracy, efficiency and regulatory compliance
- Challenges in integrating AI-driven solutions and how to overcome them
- Real-world applications of AI in streamlining workflows and enhancing safety monitoring
- Future opportunities for AI in clinical development and post-market drug safety
Xtalks Partner
PrimeVigilance
PrimeVigilance, an Ergomed Group company, was established in 2008 by Dr. Miroslav Reljanovic together with co-founder Dr. Elliot Brown. PrimeVigilance offers holistic, top quality, cost-effective, innovative clinical safety and PV services for pharmaceutical, biotechnology and medical device companies. Our leaders have an unrivalled reputation in the sector with a network of SMEs across the world. These include former senior regulators and consultants with expansive industry experience.
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