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Drug approval - Regulatory Affairs

8 courses found

Free of cost

by funding

  • Quality management in the area of drug approval (Regulatory Affairs)

    4 Weeks

  • GCP - Good Clinical Practice and QM in the area of drug approval (Regulatory Affairs)

    8 Weeks

  • GMP specialist and QM in the area of drug approval (Regulatory Affairs)

    8 Weeks

  • Quality management in the area of drug approval (regulatory affairs) and statistics

    8 Weeks

  • Quality management in the medical device industry and in the area of drug approval (regulatory affairs)

    8 Weeks

  • Regulatory Affairs (quality management in the area of drug approval) with business English

    8 Weeks

  • Project management IPMA® Level D and quality management in the area of drug approval

    12 Weeks

  • Life Science Manager and Regulatory Affairs (QM in the area of drug approval)

    16 Weeks

  • 13. January 2025

    Free seats available

  • 27. January 2025
  • 10. February 2025
  • 24. February 2025
  • 10. March 2025
Teaching Times
  • 8
  • 8
  • 0
Duration
  • 8
  • 1
  • 6
  • 1
  • 0

  • Free advice

    0800 3456-500

    Mon. - Fri. from 8 am to 5 pm
    free of charge from all German networks.

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We will gladly advise you free of charge. 0800 3456-500 Mon. - Fri. from 8 am to 5 pm
free of charge from all German networks.
Contact
We will gladly advise you free of charge. 0800 3456-500 Mon. - Fri. from 8 am to 5 pm free of charge from all German networks.