Learnaboutgmp Community

Topic	Replies	Views	Activity
Continue use of API GOOD MANUFACTURING PRACTICE (cGMP)	0	990	January 21, 2019
What is Cp & CpK? SIX SIGMA	16	4784	January 20, 2019
Lyophilizer qualification - pq protocol GOOD MANUFACTURING PRACTICE (cGMP)	0	1172	January 14, 2019
Release Notes Assessment GOOD DOCUMENTATION PRACTICE (GDocP)	0	949	January 17, 2019
Inprocess test covers for OOS investigation as per MHRA GOOD LABORATORY PRACTICE (cGLP)	0	913	January 15, 2019
Electronic Audit trail cheklist GOOD LABORATORY PRACTICE (cGLP)	0	1043	January 14, 2019
PDA Technical Report 3, Revised 2013 REGULATORY TRENDS AND QA	2	4036	January 14, 2019
Mixing after coating GOOD MANUFACTURING PRACTICE (cGMP)	3	1263	January 14, 2019
Sieve and screen qualifications GOOD MANUFACTURING PRACTICE (cGMP)	0	1112	January 9, 2019
Audit Trail - Shall the Audit Trail Keep the Record of the Access Attempt By COMPUTER SYSTEM VALIDATION (CSV)	2	1357	January 4, 2019
Stainless Steel Plate for Swab Recovery CLEANING VALIDATION	6	5244	December 26, 2018
Fluid Bed Dryer and Ethanol Content GOOD MANUFACTURING PRACTICE (cGMP)	6	1434	December 22, 2018
Validation of Needle Tip damage vision system GOOD VALIDATION PRACTICE (cGVP)	0	797	December 18, 2018
Qualification of legacy utility and equipment EQUIPMENT VALIDATION	0	1093	December 18, 2018
Validation on Dummy Environment COMPUTER SYSTEM VALIDATION (CSV)	0	1117	December 10, 2018
Open Vs Closed System COMPUTER SYSTEM VALIDATION (CSV)	6	12566	December 7, 2018
HEPA Certification Under Grade A GOOD MANUFACTURING PRACTICE (cGMP)	1	1256	December 6, 2018
What Do The cGMPs Mean By Separate Facilities? GOOD MANUFACTURING PRACTICE (cGMP)	18	7882	December 4, 2018
FBD & RMG Capacity TEMPLATES & PRESENTATIONS	3	20174	November 29, 2018
WFI distribution system 121 C hot water sanitization EQUIPMENT VALIDATION	1	1825	November 21, 2018
Autoclaving equipment using Steam/Air mixture EQUIPMENT VALIDATION	8	2805	November 16, 2018
Autoclave Qualification Acceptance Criteria EQUIPMENT VALIDATION	9	5216	November 16, 2018
Capacity calculation EQUIPMENT VALIDATION	0	1145	November 14, 2018
Vacuum pump Performance Qualification EQUIPMENT VALIDATION	2	2764	November 14, 2018
Membrane 0.2 micron filter for compressed air GOOD VALIDATION PRACTICE (cGVP)	1	976	November 12, 2018
Compressed Air for Pharma Plant GOOD MANUFACTURING PRACTICE (cGMP)	24	14147	November 10, 2018
Repetitive Deviation DEVIATION AND DISCREPANCY HANDLING	3	2134	November 10, 2018
Perforated SS 316 Plate Screen qualification GOOD MANUFACTURING PRACTICE (cGMP)	0	999	November 10, 2018
What do you do when a critical deviation is performed? DEVIATION AND DISCREPANCY HANDLING	1	1106	November 9, 2018
Manufacturing Execution Systems (MES) & Validation COMPUTER SYSTEM VALIDATION (CSV)	5	3063	October 17, 2018