As the healthcare industry continues to evolve, Artificial Intelligence (AI) is emerging as a key enabler of innovation, compliance, and operational efficiency. This webinar delves into the transformative impact of AI in the pharmaceutical and MedTech sectors, with a focus on driving efficiency through Validation, Qualification, and Testing (VQT), Good Manufacturing Practices (GMP), and overcoming data compatibility, sustainability, and scalability challenges.
We'll also explore the changing regulatory landscape, covering the implications of the EU AI Act and the FDA’s Good Machine Learning Practice (GMLP) standards on AI adoption. Participants will walk away with key insights into how to measure AI's impact and validate its benefits within clinical and healthcare workflows, ensuring both innovation and compliance.
Join this webinar to:
• Get insights into the EU AI Act and FDA’s GMLP guidelines, and their impact on AI adoption.
• Explore how AI is transforming VQT and GMP processes within pharma and MedTech sectors.
• Address the challenges related to data compatibility, scalability, and sustainability when integrating AI in healthcare.
• Learn about metrics and validation techniques to ensure AI's reliability in clinical decision support systems and healthcare workflows.
Don’t miss this opportunity to stay at the forefront of AI adoption in healthcare! Register now to secure your spot.
Panel Members:
Rahul Jain
Head of Validation and Quality
DDIT R&D, The Healthcare Business of Merck kGaA, Darmstadt, Germany
Sachin Bhandari
Head of CSV & Qualification Standards
Boehringer Ingelheim
Harshal Sawant
Practice Head – Healthcare Software Services
Tata Elxsi
Vidhya Jain
Practice Lead – Healthcare Software Services
Tata Elxsi