Date to be announced
Contact us for more infoTRAINING TIMES
Learn sophisticated methodologies for planning, executing, and documenting audits to maximize efficiency and compliance impact.
Understand diverse international GMP regulations and harmonization efforts to operate seamlessly across borders.
Apply strategies to real audits involving data integrity, cross-border compliance, and conflict resolution.
Stay ahead of industry trends and technological advancements to adapt to evolving GMP audit landscapes.
Three days of expert-led Zoom sessions packed with discussions, Q&As, and real-world scenarios.
All slides, tools, and supporting materials available in one place - before, during, and after the course.
Receive a digital certificate (also LinkedIn-ready) that verifies your skills in strategic trial planning.
Learn sophisticated methods for planning, executing, and documenting audits to ensure efficiency and compliance.
Understand and apply diverse international GMP regulations and harmonization standards to operate across regions.
Apply proven strategies to audits involving data integrity, cross-border compliance, and conflict resolution.
Enhance clarity, active listening, and conflict resolution abilities to manage challenging audit interactions.
Anticipate regulatory shifts and integrate emerging technologies to strengthen audit processes.
Designed for professionals who want to enhance their expertise and advance their careers
Associate Director – Head of Compliance Launch and Technology Center
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. In the past 6 years he worked as a QA Manager in a worldwide operating medical device and medicinal product company, as well as head of manufacturing for the production of bulk tablets. Same time he gave lectures and practiced as consultant in the fields of GMP, quality, risk management, as well as regulatory requirements in the fields of medicinal products and medical devices. On top, Felix was involved in mRNA projects in Europe concerning design, manufacturing and quality topics of mRNA processes. We are live on webchat!
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