Mastering ATMP Manufacturing: Key Principles and Practical Insights
Online Masterclass
- 23rd - 24th October 2024
- 09.00AM – 01.30PM CEST+2
Trainer
Dr. Felix Tobias Kern
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Introduction
This two-day course offers advanced insights into the manufacturing of Advanced Therapy Medicinal Products (ATMPs), catering to both experienced professionals and beginners seeking an overview of the field. Emphasizing strategies for success and adherence to regulatory standards, including the EU-GMP guide, industry experts will guide participants through ATMP fundamentals, manufacturing processes, risk management, essential operations, quality assurance, and advanced techniques.
Through interactive sessions, breakout discussions, and Q&A sessions, attendees will gain practical knowledge and skills essential for effective ATMP production. Designed for professionals in the pharmaceutical and biotechnology industries, this course provides a comprehensive understanding of ATMP manufacturing, equipping participants with the tools needed to navigate challenges and optimize production processes while ensuring compliance with industry standards. Join us to elevate
your expertise in ATMP manufacturing and ensure compliance with regulatory requirements.
Who Should Attend
- Experienced professionals and novices in pharmacy and biotechnology
- Employees in pharmaceutical and biotechnology industries, particularly those in ATMP production, quality control, and regulatory compliance.
- Regulatory compliance experts
- Specialists in risk management, quality assurance, and process optimization.
- Quality control specialists, production managers, regulatory affairs personnel, and research scientists in pharmaceutical development
Meet The Trainer
Dr. Felix Tobias Kern is Associate Director at the Merck KGaA in Darmstadt (Germany). He studied pharmacy in Mainz (Germany) and graduated at the Ludwig-Maximilians-University in Munich. He is expert pharmacist for pharmaceutical analytics and pharmaceutical technology.
In the past 10 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
