Revision history of "Cleanroom training" (Q3542887)

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22 March 2024

16 February 2024

20 June 2023

12 June 2023

15 July 2022

  • curprev 21:5921:59, 15 July 2022DG Regio talk contribs 48,261 bytes +31,520 Changed label, description and/or aliases in da, el, hr, ro, sk, mt, pt, fi, pl, sl, cs, lt, lv, bg, hu, ga, sv, et, nl, fr, de, it, es, and other parts: Adding translations: da, el, hr, ro, sk, mt, pt, fi, pl, sl, cs, lt, lv, bg, hu, ga, sv, et,

23 January 2022

20 January 2022

21 December 2021

9 December 2021

21 November 2021

18 November 2021

17 November 2021

  • curprev 23:1223:12, 17 November 2021DG Regio talk contribs 9,440 bytes +77 Changed label, description and/or aliases in en: translated_label
  • curprev 23:1223:12, 17 November 2021DG Regio talk contribs 9,363 bytes +1,460 Created claim: summary (P836): High standards (Good Manufacturing Practice-GMP) and extensive legal requirements must be met in order to ensure the protection of patients and other users when manufacturing products for medical technology that can affect people’s health and quality of life in the broadest sense. Therefore, extensive training is necessary for the employees, who work in the cleanroom areas and monitor the production. These trainings include validation, qu...

7 November 2021

6 November 2021