GMP Auditing for Quality Assurance Training Course for FDA Regulated Industries (ONLINE EVENT)

Core Insights - The training course on GMP Auditing for Quality Assurance is designed to enhance auditing skills in the pharmaceutical industry, focusing on compliance with FDA regulations and quality standards [1][2] Group 1: Training Course Details - The GMP Auditing course will take place on January 28th - 29th, 2026, and aims to equip professionals with the necessary competencies for effective auditing [1] - The course includes a comprehensive overview of GMP regulatory frameworks, types of audits, and audit planning [5] - Participants will receive a certificate of participation, presentation slides, and free handouts on GMP Auditing [6] Group 2: Learning Objectives - Attendees will learn to evaluate audit findings, identify critical components for audit reports, and conduct audits using trails and checklists [6][10] - The course covers the importance of GMP in quality assurance and the role of auditing in compliance and risk management [6] - Key topics include internal audits, supplier audits, regulatory inspections, and developing effective audit plans [6][9] Group 3: Target Audience - The training is suitable for QA/QC professionals, regulatory compliance managers, manufacturing supervisors, GMP auditors, and anyone responsible for GMP compliance in pharmaceuticals, supplements, or food industries [6][7] Group 4: Expert Instructors - The course will be led by Kelly Thomas, who has over 20 years of experience in cGMP and quality systems within the pharmaceutical and medical device sectors [7][8] - Ms. Thomas's expertise includes validation processes, risk-based approaches, and managing complex projects [8]