OBJECTIVE To lay down a procedure for Environmental Monitoring of Manufacturing Area. 2. SCOPE...
Mfg
1-OBJECTIVE To lay down a procedure for product recall. 2-SCOPE This procedure is applicable for Product recall...
Cleaning Validation Manufacturing Facility & equipment – Manufacturing facility is nothing different, the same principles apply....
In Pharmaceutical Industries human error and its reduction is very bib challenge. During regulatory audit most of...
Audit Trail: “An audit trail (also called audit log) is a security-relevant chronological record, set of records, and/or destination and source...
Introduction: Cleaning Validation is very important topic in Pharmaceutical Industries. Our cleaning procedure and cleaning validation should...
Brief: In any pharmaceutical organization compliance of 21 CFR part 11 is very important and basic requirements...
1.0 OBJECTIVE: To lay down a procedure for investigation and evaluation of out-of-specification test results obtained...
In Pharmaceutical Industries, it’s is very important to know the guidance for significant figure and rounding of...
In Pharmaceutical Industries generally following investigation tools are used by investigator- Different Investigation tools: A-5W and 1-How:...
