GMP Lead Auditor - Online GMP Certification
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    GMP Lead Auditor

    Advanced Strategies and Future Trends in GMP Auditing

    19-21 March 2025, live online training

    Summary

    Dive into the World of Advanced Strategies and Future Trends in GMP Auditing! Join us for our exclusive webinar tailored for professionals in the pharmaceutical, biotech, and medical device industries who are keen on elevating their GMP auditing skills. Immerse yourself in an engaging and informative experience as we delve into a variety of topics aimed at deepening your understanding and refining your approach to GMP auditing. Through interactive case studies, you’ll have the opportunity to dissect real-world scenarios, gaining practical insights into navigating complex audit situations. Benefit from expert insights shared by industry leaders, providing you with valuable perspectives and strategies to stay ahead in the ever-evolving landscape of GMP regulations. Participate in hands-on workshops designed to equip you with the tools and techniques necessary to excel in GMP auditing, ensuring you are well-prepared to meet the latest requirements and adhere to best practices. Don’t let this opportunity pass you by! Register now to expand your expertise, connect with fellow professionals, and position yourself as a leader in the field of GMP auditing.

    Learning Objectives

    • Understand advanced strategies for planning and executing GMP audits effectively
    • Gain insights into global GMP compliance requirements and harmonization efforts
    • Enhance problem-solving skills through interactive case studies on complex audit scenarios
    • Develop a comprehensive understanding of advanced FDA regulations and compliance expectations
    • Learn strategic approaches to navigate FDA compliance challenges through interactive sessions
    • Acquire techniques for thorough classification and impact assessment of audit findings
    • Master essential skills for expert GMP auditors, including regulatory knowledge and effective communication
    • Improve communication proficiency during audits through practical workshops and role-playing exercises
    • Explore future trends and innovations in GMP audits, enabling strategic planning and adaptation to regulatory changes

    Key Topics

    • Advanced GMP Audit Strategies: Detailed exploration of sophisticated methodologies for planning, executing, and documenting GMP audits, focusing on efficiency and effectiveness
    • Global GMP Compliance: In-depth analysis of international GMP regulations and harmonization efforts, emphasizing the importance of aligning with diverse regulatory requirements
    • Interactive Case Studies on Complex Audit Scenarios: Examination of real-world audit scenarios, facilitated by industry experts, to enhance problem-solving skills and decision-making capabilities in challenging situations
    • Advanced FDA Requirements and Regulatory Expectations: Comprehensive review of advanced FDA regulations and expectations, providing insights into compliance strategies and risk mitigation techniques
    • Strategic Navigation of FDA Compliance: Interactive case studies focusing on FDA compliance challenges, encouraging participants to develop strategic approaches and share best practices
    • Thorough Classification and Impact Assessment of Audit Findings: Detailed categorization and evaluation of audit findings to prioritize corrective actions effectively and drive continuous improvement initiatives
    • Essential Skills for Expert GMP Auditors: Identification of core competencies required for GMP auditors, including regulatory knowledge, analytical abilities, and effective communication skills
    • Mastering Communication Techniques for GMP Auditors: Practical workshop aimed at enhancing communication proficiency during audits, covering strategies for clarity, active listening, conflict resolution, and role-playing exercises
    • Future Trends and Innovations in GMP Audits: Exploration of emerging trends and technological advancements shaping the future of GMP auditing, with a focus on strategic planning and regulatory forecasting

    Who should attend?

    Everyone who is concerned with GxP audits, for example:

    GMP Auditors, QA Professionals, CMO and CLO Managers and Representatives, Manufacturing Experts, Quality Control Experts, Regulatory Affairs Managers, Validation Experts, Supply Chain Managers, Sales Representatives, IT Managers in the fields of GxP, EHS Managers.

    The course is designed for advanced expert GMP auditors.

    Our online training experience includes

    • Our client zone – a single source for all training materials as well as pre and post-training communication
    • Live interactive format via the Zoom platform
    • Direct interaction with the trainer
    • Q&As, case studies, polls
    • Revisit recorded sessions for 7 days
    • Training in digital format
    • Digital and LinkedIn certificates

    Trainers

    quality, biotech, biologics, regulatory
    Dr. Felix Tobias Kern is the Associate Director - Head of Compliance Launch and Technology Center at the Merck KGaA in Darmstadt (Germany). He studied pharmacy in Mainz (Germany) and graduated at the Ludwig-Maximilians-University in Munich (Germany). He is an expert pharmacist for pharmaceutical analytics and pharmaceutical technology.

    Advanced Strategies and Future Trends in GMP Auditing

    Download the full training agenda to reveal complete session details, training takeaways, case studies, daily schedule, special features and full trainer bio.

    Online Participation
    1 850  Price incl. VAT: 1 850 

    Price per delegate including:

    Online participation

    Online workbook & materials

    Certificate

    PC, microphone, camera, stable internet connection and the Zoom application.

    Yes, we will make every effort to ensure best possible interaction. You will see the slides, interact with the trainer and fellow participants. Questions and group exercises will be facilitated through the online meeting platform.

    Yes, you can transfer the registration to a colleague at any time.

    Yes, you may transfer your registration to a different event up to one month before the scheduled dates, provided the training fee has been paid in full.

    pharma learning leader

    Lydia Makori

    l.makori@symmetric.events
    +421 222 200 543

    Training Details
    • Start Date
      19. March 2025
      01:30 PM Vienna time
      12:30 PM London time
      08:30 AM New York time
      05:30 AM Los Angeles time
    • End Date
      21. March 2025
    What participants said about Symmetric courses

    "I was happily pleased with the enormous experience of the trainer, i enjoyed it a lot and learned a lot."
    Senior Development Pharmacist, Orion Corporation

    "Keep up the excellent standard of training courses!"
    FDF Industrialisation Manager, Medichem Manufacturing

    "I have received a lot of knowledge that will be of big use for my profession."
    Quality manager, Vironova AB

    "Thank you for a very informative training course. The timing of start/break/finish was perfect."
    Clinical Project Manager, Regen Lab

    "Would highly recommend this course, great practical insights throughout helped to make it all very real, many thanks."
    Head of API and Contract Manufacturing, Zentiva Group

    "Very informative and memorable training course for me."
    Quality Vice President, Darou Pakhsh

    "The trainer was very knowledgeable about the topics and was able to answer all questions."
    Drug Product Subject Matter Expert, Pfizer