25 Aug
|
Troikaa Pharmaceuticals
|
India
25 Aug
Troikaa Pharmaceuticals
India
Review of electronic data for Finished product, stability samples, AMV, RM, PM, water and EM as per review checklist, raw data, worksheet, working standards/reference standards details, instruments calibration status, acceptance criteria as per specification and MOA verify and update observations.
Prepared and Review of stability summary reports.
Review of URS, DQ, IQ, OQ, PQ documents of QC instruments.
To review of OOS, OOT, lab deviation and lab incident investigation reports.
📌 Qa Aqa Analytical Quality Assurance Api Dahej (India)
🏢 Troikaa Pharmaceuticals
📍 India