22 July - 15:00 - 16:00 BST / 10:00 - 11:00 ET / 16:00 – 17:00 CET
The Future is Now – Transforming Regulatory Processes with AI, ML, NLP, and RPAs
In today's rapidly evolving regulatory landscape, staying compliant and efficient is more challenging than ever. Join us for an exclusive webinar where we explore how cutting-edge technologies like Artificial Intelligence (AI), Machine Learning (ML), Natural Language Processing (NLP), and Robotic Process Automation (RPA) are revolutionizing regulatory processes. Discover how these innovations can streamline workflows, enhance decision-making, and ensure continuous compliance, helping your organization maintain a competitive edge.
Learning Outcomes
• Understand the Basics: Gain a foundational understanding of AI, ML, NLP, and RPA and their applications in regulatory affairs.
• AI/ML-Enabled Workflows: Discover how AI and ML can automate routine tasks, enhance decision-making, and provide dynamic task management.
• AI-Assisted RIMS: Understand how AI can improve compliance monitoring, streamline document generation, and provide personalized regulatory insights.
• Automated Content Generation: See how predictive and generative AI can create regulatory submission documents, automate quality checks, and ensure data accuracy.
• Explore RIA: Learn how IQVIA Regulatory Intelligence Assistant (RIA) leverages AI and extensive regulatory intelligence data to provide accurate, real-time insights.
Target Audience
• Regulatory Affairs Managers
• Compliance Officers
• Quality Assurance Managers
• Clinical Research Associates
• Medical Writers
• Regulatory Intelligence Analysts
• Pharmacovigilance Specialists
• Regulatory Operations Managers
Speakers
Michelle Gyzen
Michelle has over 20 years of experience in pharmaceuticals, biotech, and medical devices. A senior director with expertise in designing large-scale regulatory outsourcing programs, offshore resource modeling, and regulatory tech integration and automation. In her current role, Michelle is involved in designing strategic solutions for regulatory, focused on operational efficiency, scalability, and technology.
Kiran Chinnalla
Kiran has over 17 years of experience in global regulatory affairs and technology enablement. As a Product Manager specializing in advanced Generative AI and RPA applications for Regulatory Intelligence, automated content generation, and process automation, Kiran excels in regulatory strategy, labeling, medical and scientific writing, pharmacovigilance, and technology transformation. With a strong background in global regulatory affairs and extensive experience in the pharmaceutical & healthcare industries, Kiran holds a Master's in Pharmacology and Toxicology.
Ankit Tyagi
Ankit has over 15 years of experience in global regulatory affairs. A seasoned program manager with a master’s in business administration and an MS in pharmacoinformatic with diverse experience in handling regulatory strategy, lifecycle maintenance and post-approval submissions, labeling and RIMS Data Management. In his current role, Ankit is involved as a project oversight for strategic lifecycle maintenance projects.
This webinar is sponsored by IQVIA
Disclaimer: Whilst TOPRA is running this webinar for IQVIA, this is not an endorsement of IQVIA, IQVIA's affiliates, employees or its products and services. TOPRA is also not responsible for the content or views expressed during the webinar.
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Pricing
- Members: free
- Non-members: free
Terms and Conditions
By purchasing this webinar, you are agreeing to TOPRA's training terms and conditions.