Quality Assurance


Topic Replies Activity
CGMP Annual Refresher training 1 July 17, 2019
Preparation of Documents 1 July 17, 2019
Purified water toc 6 July 17, 2019
Cleaning Validation 3 July 15, 2019
Fungal growth in sterile 7 July 14, 2019
Media fill validation 3 July 13, 2019
HPLC Calibration 1 July 13, 2019
Why 6.5 gm required to do a friablity test for tablets 5 July 13, 2019
Mock Recall procedure 1 July 11, 2019
Dynamic Pass box class 2 July 11, 2019
Integrity test/Inprocess test -Media fill 3 July 11, 2019
Standard Test Procedures for syrup 5 July 10, 2019
What is the importance of IPQA in pharmaceutical 4 July 9, 2019
Method validation 3 July 7, 2019
Particle Size Sieve Analysis 2 July 7, 2019
How to classify a equipment 3 July 6, 2019
Risk Assessment Procedure 2 July 6, 2019
RM vendor Qualification 2 July 6, 2019
PH of the resulting solutions 1 July 2, 2019
Dissolution Apparatus 6 July 1, 2019
Cleaning validation 3 June 27, 2019
Risk assessment of dry heat sterilizer autoclave, and Hplc 2 June 24, 2019
Stand alone CAPA 3 June 22, 2019
API chemical store 2 June 22, 2019
Plant layout for finished formulations 4 June 20, 2019
Media fill simulation 2 June 18, 2019
Particulate measuring system-liquids eye drops 1 June 18, 2019
Extension of Media fill periodic validation 1 June 18, 2019
Equipment qualifications 3 June 18, 2019
Instrument Calibration 4 June 18, 2019