Quality Assurance


What is the BPR and review & Dispensing Activity? (6)
What is COPP & some details of FDA Documentation? (3)
Hold time of unfiltered sterile product formulation (2)
Fitration process - sterile eye drops ( 2 ) (37)
SIP Mapping- Maximum allowable temperature (7)
Cleaning validation (7)
HOLD TIME STUDY (3)
Planned Power shut down for 2 weeks and power resume (14)
Stability sample in first b (3)
Market complaint related to packaging (2)
Finished product sampling (2)
Recommissioning of equipment (3)
Equipment Dirty Holding Time (3)
Employee medical checkup (1)
Deviation and change control (8)
Hardness tester failure (1)
Stability study of intermediate condition (1)
Quality check of media used in microbiological analysis with examples of positive and negative control organism of individual media? (2)
Air particle counter equipment qualification (IQ and OQ) (3)
ISO 13485 quality system principle (2)
Audit and Inspection of new Pharma company (2)
Analysis of Detergent Powder (1)
BMR preparation (6)
Method Validation (1)
Same Material Entry and Finished Product Exit Area (6)
Need few information regarding QA department (4)
Procedure of Dispensing (5)
Reuse of sample in IPQA test (2)
1 micron particles (1)
About Non - Conformance (2)