SCHEDULE M – GMP – PART 1
GOOD MANUFACTURING PRACTICES – SCHEDULE M
SCHEDULE M – GMP – PART 1 Read More »
QA
Self Inspection Checklist
Self inspection checklist for Raw Material, Packaging Material, Quality Assurance, Quality Control, Microbiology Dept, Engineering Dept.
Self Inspection Checklist Read More »
Rinse and Swab Sampling From Equipment’s Product Contact Surface SOP
SOP for Rinse and Swab Sampling From Equipment’s Product Contact Surface.
Rinse and Swab Sampling From Equipment’s Product Contact Surface SOP Read More »
Allocating identification number to instrument / equipment / utility
SOP For Allocating identification number to instrument / equipment / utility
Allocating identification number to instrument / equipment / utility Read More »
Specimen Signature SOP
Standard Operating Procedure for Specimen Signature in Pharmaceutical Industries.
Specimen Signature SOP Read More »
User Requirement Specification Example – InstrumentÂ
Example of filled User Requirement Specification – InstrumentÂ
User Requirement Specification Example – Instrument Read More »
Preparation of User Requirement Specification (URS) SOP
SOP for Preparation of User Requirement Specification – URS in Pharmaceutical industries.
Preparation of User Requirement Specification (URS) SOP Read More »
Handling of Out Of Trend (OOT) SOP
SOP For Handling of Out Of Trend (OOT)
Handling of Out Of Trend (OOT) SOP Read More »
Out of Specification Flow Chart of Investigation for different Phases
Out of Specification Flow Chart of Investigation for different Phases
Out of Specification Flow Chart of Investigation for different Phases Read More »
Flowchart for Quality Risk Management and Quality Risk Management Process
Flowchart for Quality Risk Management and Quality Risk Management Process
Flowchart for Quality Risk Management and Quality Risk Management Process Read More »