Artificial Intelligence (Al) in Manufacturing FDA-Regulated Products
Date: Novernber 25, 2024
Duration: 60 Minutes
Time: 12 PM EST
The FDA recognizes the immense potential of AI in improving manufacturing reliability, supply chain resilience, and overall product quality. With the establishment of the Emerging Technology Program (ETP) in 2014, the FDA has demonstrated its commitment to supporting companies in integrating advanced manufacturing methods, including AI.
Why should I attend:
- Optimizing Process Design and Control: Discover how AI can streamline the design and control of manufacturing processes, leading to higher efficiency and lower costs.
- Smart Monitoring and Maintenance: Learn how AI-driven monitoring systems can identify and address potential issues before they become critical, ensuring continuous production with minimal downtime.
- Process Monitoring and Fault Detection: Explore how AI-powered algorithms can detect anomalies and deviations in real-time, ensuring product quality and compliance.
- Trend Monitoring for Continuous Improvement: Harness the power of AI to analyze trends and patterns in manufacturing-related deviations, driving continuous improvement in your manufacturing practices.
- Real-World Examples and Case Studies: Our seminar isn’t just about theory; it’s about real-world applications. Throughout the event, we’ll showcase successful AI integration examples and provide case studies based on interactions and published information. Witness how AI can be used in Process Design and Scale-up, Advanced Process Control (APC), Process Monitoring and Fault Detection, and Trend Monitoring in actual pharmaceutical manufacturing settings.
- Regulatory Affairs Professionals
- Quality Assurance Professionals
- Clinical Research Professionals
- Principal Investigators
- Site Managers and Research Coordinators
- Contract Research Organizations (CROs) Staffs
- Institutional Review Board (IRB) Members
- Drug discovery and development professionals (R&D and CMC)
- Clinical trial managers
- Project Managers and Clinical trial specialists
- Pharmaceutical and Biotech Industry Professionals involved in clinical trial planning and execution.
Don’t miss this exclusive opportunity to stay ahead in the fast-paced pharmaceutical industry. Reserve your spot for our AI in Manufacturing FDA Regulated Products Seminar now! Seats are limited, so secure your place early.
Let’s shape the future of pharmaceutical manufacturing together. See you at the seminar!
Speaker: Mukesh Kumar
PhD, RAC | CEO, FDAMap
For more info, fill the box below. We will contact you within 24 hrs.
Webinar Fee
Prices are in US Dollars.
The registration fee includes: The live webinar & all related course materials.
Terms & Conditions to register for the Webinar
Your Registration for the workshop is subject to following terms and conditions. If you need any clarification before registering for this webinar please email us at info@fdamap.com
Payment
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Cancellations & Substitutions:
Written cancellations through fax or email (from the person who has registered for this conference) received at least 5 business days prior to the start date of the event will receive a refund — less a $30 administration fee. No cancellations will be accepted — nor refunds issued — within 5 business days before the start date of the event. You may however, choose to substitute the webinar for which you are registered with some other webinar in the future.
On request by email or fax (before the seminar) a credit for the amount paid minus administration fees ($30) will be transferred to any future FDA Map event and a credit note will be issued. No-shows will be charged the full amount.
Webinar material will be uploaded on the website 24 hours before the scheduled date of the webinar. In case it is not available on the website due to some technical issues, we will email the material a few hours before the start of the webinar.
In the event FDA Map cancels the webinar, FDA Map will issue a full refund to all the registrants for that webinar. Some topics and speakers may be subject to change without notice.
