Qualification of climatic equipment, systems for the production and distribution of pharmaceutical gases, quality control of pure steam

Qualification of climatic equipment, systems for the production and distribution of pharmaceutical gases, quality control of pure steam

Details

  • Start date: 05 December 2022
  • Start time: 10:00 (Kyiv)
  • Finish date: 05 December 2022
  • Finish time: 14:30 (Kyiv)
  • Duration: 4 hours
  • Break: yes
  • Category: Production (GMP)
  • Format: Streaming
  • Online broadcast available: yes
  • Venue: Online
  • Language class: Русский
  • Cost for connecting to the webinar of one computer (participant): $173.

    VAT is not paid.

    $87 discounted price:

    – for each subsequent participant from one organization;

    – students, subject to the presentation of a student card.

    $121 discounted price:

    – clients of the Conformity Assessment Body UKRMEDCERT LLC and GXP UMEDCER LLC.

     

    The price includes: information service, video recording of the webinar, a set of training materials and a certificate in pdf format.

     

    Target audience: authorized persons, quality directors, persons responsible for the implementation and operation of the quality management system, specialists in the qualification and validation of enterprises engaged in economic activities for the production and wholesale of medicines.

     

    Webinar program:

    1. Regulatory framework.

    2. Terms and definitions.

    3. Validation of warehouses. Approaches to temperature mapping.

    4. Vehicle qualification. Features of the organization of the process. Process optimization.

    5. Qualification of climate technology (refrigerators, refrigerators, Frigo chambers, freezers, low-temperature climate technology).

    6. Qualification of thermal containers. Classic mistakes.

    7. Qualification of systems for the production and distribution of pharmaceutical gases (compressed air, compressed nitrogen).

    8. Checking the quality of pure steam (Steam Quality Test). Practical aspects of testing.

    9. Conclusion.