Regularly I act as a speaker at conferences, seminars or other events. My lectures are related to:

  • Medical Devices and (Drug/Device) Combination Products
    • Development and Design Control (according to EN ISO 13485/21 CFR Part 820.30)
    • Quality Management (according to EN ISO 13485/21 CFR Part 820), including Post-Market Surveillance, Vigilance requirements
    • Risk Management (according to EN ISO 14971)
  • Pharmaceutical packaging
    • Regulatory Requirements
    • Development
    • Quality Control (e.g., Specifications, Defect Evaluation Lists, AQL, Test methods, Planning and conducting incoming goods inspection)
  • specific Products and Technologies
    • Pre-filled syringes (PFS)
    • Medical Software / Medical Apps
    • Use of Radio Frequency Identification (RFID) in the healthcare environment
My presentations are either in German or English language.
An overview over upcoming and past lectures is given below.

Upcoming lectures

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Past lectures

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