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ÀÇ·á±â±â ¹Ì±¹ FDA cGMP ½Ç¹«(24³â 2Â÷)

  • °úÁ¤ºÐ·ù :  °í±Þ
  • ±³À°ÀÏÁ¤ :  2024-11-19 ~ 2024-11-20
  • ±³À°ÀÚ°Ý :  ÀÇ·á±â±â Ç°Áú°ü¸® Á÷¹« ÀçÁ÷ÀÚ
  • ¸ðÁýÀοø :  30¸í
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  • ÷ºÎÆÄÀÏ :  file4 [KMDA]FDA cGMP ½Ç¹«_11¿ù.pdf

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¡á °ú Á¤ ¸í : ÀÇ·á±â±â ¹Ì±¹FDA cGMP ½Ç¹«(24³â 2Â÷)

¡á ±³À°±â°£ : 2024. 11. 19(È­) ~ 2024. 11. 20(¼ö)

¡á ±³À°½Ã°£ : 09:30~17:30 (1ÀÏ 7½Ã°£ / ÃÑ 14½Ã°£)

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¡á ±³À°Àοø : 30¸í   

¡á±³À°Æ¯Àü : ½Ä±Ç, ±³Àç ¹«»óÁ¦°ø ¹× ¼ö·áÁõ ¹ß±Þ

 

* Á¢¼öÀÏ : 2024.10.31 (¸ñ) 10:00~

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1ÀÏÂ÷ (09:30 ~ 17:30) 

- ¹Ì±¹ cGMP inspection ÇÁ·Î¼¼½º (1½Ã°£)

- ¹Ì±¹ cGMP inspection ÇÁ·Î¼¼½º(21 CFR Part820 -Management control) (2½Ã°£)

- ¹Ì±¹ cGMP inspection ÇÁ·Î¼¼½º(21 CFR Part820 -Corrective and Preventive Actions (2½Ã°£)

- ¹Ì±¹ cGMP inspection ÇÁ·Î¼¼½º(21 CFR Part820 -Corrective and Process Controls (2½Ã°£)

 

2ÀÏÂ÷  (09:30 ~ 17:30) 

¹Ì±¹ cGMP inspection ÇÁ·Î¼¼½º(21 CFR Part820 -Material Controls) (1½Ã°£)

¹Ì±¹ cGMP inspection ÇÁ·Î¼¼½º(21 CFR Part820 -Documents/REcords/Change Control) (1½Ã°£)

- ¹Ì±¹ eMDR µî·Ï ÇÁ·Î¼¼½º (1½Ã°£)

- Á¦Ç°À̷±â·Ï(DHR)ÀÛ¼º »ç·Ê¿¬±¸ (1½Ã°£)

¹Ì±¹ cGMP ÁöÀû»çÇ× »ç·Ê¿¬±¸ (1½Ã°£) 

483 Observation ÈļÓÁ¶Ä¡ »ç·Ê¿¬±¸ (2½Ã°£)

 

* Áᫎ : 12:30~13:30

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