mRNA

    Manufacturing of mRNA-Based Therapeutics

    22 – 24 June 2022, live online training

    Summary

    This 3-day online training is a deep dive into the world of messenger ribonucleic acid (mRNA). You will obtain detailed information about the manufacturing and quality characteristics and intensify your know-how about the process of scaling up and the transfer of know how from the development stage to the market manufacturing stage.

    Learning Objectives

    • Understand the regulatory landscape
    • Overview over GMP and quality requirements for the manufacture of mRNA medicinal products
    • Learn about development and the basic requirements for manufacturing
    • How to manage facilities, utilities and equipment?
    • Modern cross contamination prevention concepts
    • Modern process validation concepts
    • How to implement effective process changes?
    • Implementation of analytical methods
    • How to implement a good In-Process Control concept?
    • Tech transfer from the development to the market manufacturing department

    Key Topics

    • Regulatory framework
    • Quality & GMP requirements
    • Manufacturing of the drug substance
    • Sterile filling
    • Process validation
    • Managing process changes
    • Analytical methods
    • Release specification vs IPC requirements

    Who should attend?

    Quality Assurance and Quality Control Manager, Regulatory Affairs Manager, Process Validation Specialist, Manufacturing Management, Process Development, Research and Development

    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 30 days
    • Training in digital format
    • Digital and LinkedIn certificates

    Trainers

    quality, biotech, biologics, regulatory
    Head of Manufacturing
    Dr. Felix Tobias Kern is Head of Manufacturing 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.
    Fritz Roder
    Global Engineering Manager
    Fritz Röder is Global Engineering Manager at Merck KGaA in Germany and is a recognized expert in the pharmaceutical industry. He has large experience in pharmaceutical media supply, GMP environments and the processing of solid, semisolid and liquid (sterile) dosage forms.

    Manufacturing of mRNA-Based Therapeutics

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

    Online Participation
    1 650  Price incl. VAT: 1 650 
    Equivalent of approx. 1 777 USD.
    The price calculation in USD is informative and might slightly differ from your bank exchange rate
    .

    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
      22. June 2022
      09:00 AM Vienna time
      08:00 AM London time
      03:00 AM New York time
      12:00 AM Los Angeles time
    • End Date
      24. June 2022