1.GMP documents review, approve, effective and issuance.
2.Logbook and Notebook management.
3.MBR and PBR issuance.
4.Document retrieval
5.Tracking revised SOP and MBR/PBR Training.
6.Lock the data sheets of QC analysis method.
7.二級包材規格確認及審核
8.協助線上系統管理