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Acceptance Criteria for AI Validation: Determining What “Reliable” Actually Means in GxP SystemsAI-enabled systems are b...
08/31/2026

Acceptance Criteria for AI Validation: Determining What “Reliable” Actually Means in GxP Systems

AI-enabled systems are bringing new challenges to validation. When outputs can vary, how can organizations define and demonstrate reliability, trust, and fitness for intended use?

Join the Conference Panel and Carolyn Troiano for a 1-Day In-Person Seminar focused on practical, risk-based approaches to validating AI-enabled GxP systems.

📅 September 23, 2026
⏰ 9:00 AM – 5:00 PM EST
📍 Piscataway, NJ

Key topics include:
• FDA compliance and enforcement trends for AI
• CSV, CSA & GAMP 5, 2nd Edition
• 21 CFR Part 11 & Data Integrity
• AI acceptance criteria and risk-based validation
• AI shortcomings, including hallucinations, bias & drift
• Expert-in-the-Loop and critical thinking
• Vendor audits & inspection readiness
• Industry best practices for AI validation

🎤 Speaker: Carolyn Troiano — 45+ years of experience across FDA-regulated industries.

🔗 Learn more & register: https://conferencepanel.com/seminar-detail/acceptance-criteria-for-ai-validation-determining-what-reliable-actually-means-in-gxp-systems

A valuable opportunity for professionals involved in AI governance, CSV/CSA, QA/QC, compliance, validation, and regulatory operations.

08/27/2026

Why Are U.S. Professionals Turning to Expert Insights?

Gain practical U.S. industry insights from experts who help professionals understand changes faster, avoid costly mistakes, and make better decisions.

Check out www.conferencepanel.com now.
For expert consultation, call us at 📞+1-(877) 629-3710

08/26/2026

Why U.S. Professionals Should Be Ready Before Monday

Get ahead of the U.S. workweek with live expert training that answers real questions, builds practical skills, and helps professionals make better decisions before Monday begins.

Check out www.conferencepanel.com now.
For expert consultation, call us at 📞+1-(877) 629-3710

🔬 Today’s Webinar: Sterile Filtration of Pharmaceutical Products – Validation and Regulatory RequirementsSterile filtrat...
08/25/2026

🔬 Today’s Webinar: Sterile Filtration of Pharmaceutical Products – Validation and Regulatory Requirements

Sterile filtration is a critical component of sterile pharmaceutical manufacturing—and effective sterility assurance depends on much more than simply selecting the right filter.

Today’s webinar will provide a practical look at the design, validation, testing, and regulatory expectations surrounding pharmaceutical sterile filtration systems.

Key areas covered include:
• Sterile filtration system design and filtration media
• Sterilization methods, including SIP and autoclaving
• Microbial retention challenge testing
• Filter integrity testing and media qualification
• Product compatibility and extractables/leachables
• Operating parameters such as pressure, time, and temperature
• Potential concerns involving fibers, endotoxins, and product impact
• FDA and EU GMP regulatory requirements
• Responsibilities of filter manufacturers and pharmaceutical users

The session will also examine use-point compressed air filtration, engineering considerations, and the validation approaches needed to demonstrate reliable microbial retention.

Register, https://conferencepanel.com/conference/sterile-filtration-of-pharmaceutical-products-validation-and-regulatory-requirements

A valuable session for pharmaceutical professionals involved in sterile manufacturing, filtration validation, contamination control, and GMP compliance.

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