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DESCRIPTION:https://fleming.events/new-ich-and-ema-quality-guidelines/\n\n
 In summary\, this course will help the delegates to identify important ne
 w GMP and Regulatory aspects which should be considered throughout the en
 tire life cycle of their specific products and avoid waste of time and mo
 ney\, thereby.\n\nKey topics: \n\n\nICH Q12 Lifecycle Management\nICH Q13
  Continuous Manufacturing\nEMA Guideline on quality documentation for med
 icinal products when used with a medical device\nICH Q14 Analytical Proce
 dure Development\nICH Q2(R2) Analytical Validation\nCurrent EMA Quality D
 iscussions and Initiatives\n\nTraining audience: \n\n\nRegulatory affairs
 \nQA/QC\nAnalytical Development\nR&amp\;D Scientists\nManufacturing Scien
 tists\nCMC\nGMP\nRegulators\n\n&nbsp\;\n\n&nbsp\;\n
DTEND:20230224T180000
DTSTAMP:20260514T153457Z
DTSTART:20230223T140000
LOCATION:\,
SEQUENCE:0
SUMMARY:https://fleming.events/new-ich-and-ema-quality-guidelines/\nIn sum
 mary\, this course will help the delegates to identify important new GMP 
 and Regul...
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