Non-compliance is a costly risk that healthcare companies cannot afford. To avoid product approval delays, recalls, and adverse impacts on shareholder value, companies must establish robust GxP compliance strategies and risk mitigation approaches. This seminar will cover the essential strategies for ensuring compliance with GCP, GLP, GMP, and other FDA regulations. We'll discuss how to implement a risk-based approach to managing quality and regulatory compliance, emphasizing the importance of effective risk management, document control, compliance training, ongoing auditing, and monitoring activities.
This two-day seminar is designed to equip pharmaceutical, biopharmaceutical, biologics, and medical device professionals with the necessary tools to efficiently manage FDA inspections. Learn the fundamentals of preparing for and surviving FDA inspections, whether you are a Class I, II, III device manufacturer or a pharmaceutical or biologics producer. The course will cover the do's and don'ts of FDA inspections, including interviewing techniques, responding to questions, reviewing documentation, and handling 483's and Warning Letters. We will also explore the procedures for hosting and following up on inspections, ensuring readiness, and managing scheduled or unscheduled inspections.
In addition to FDA inspections, this seminar will provide insights into inspections conducted by international and non-FDA agencies, including self-inspections and mock audits. Participants will learn how to prepare for inspections, handle them effectively, and understand the follow-up process. This comprehensive training will ensure all employees are aware of inspection procedures, minimizing surprises and enhancing compliance.
WHY YOU SHOULD ATTEND | WHO SHOULD ATTEND | |
Attending this seminar will enable you to define and execute proven GxP compliance strategies, ensuring operational readiness and optimal pathways during inspections. You will learn to identify visible signs of GxP compliance and demonstrate risk-based awareness, improving credibility and trust with FDA and other regulators. Gain a deeper understanding of how to interact and communicate effectively with the FDA, learning the ground rules and do's and don'ts of FDA inspections. This seminar will cover critical training areas in GxP compliance, helping you understand what the FDA can and cannot request during an inspection. Learn the importance of pre-inspection planning and how to navigate the inspection process from preparation to close-out. Understand the FDA's authority and processes, including handling 483s, Warning Letters, and recalls. Explore the benefits of mock audits and the required documentation, formats, and archiving methods. By attending, you will learn how to respond to inspection and audit results, discussing pain points and challenges in a group setting to find workable solutions for FDA inspections. Prepare for interactive discussions and a mock inspection exercise to enhance your skills in communicating with the FDA and referencing FDA guidance and resources. This seminar is essential for anyone involved in FDA-regulated industries, providing the knowledge and tools to ensure your company remains compliant and prepared for any inspection. |
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AGENDA | ||
DAY 1 (9 AM to 2 PM) ecture 1: Introduction and FDA Inspection Authority
| DAY 2 (9 AM to 2 PM) Lecture 1: Maintaining Regulatory Compliance
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