Gap Analysis For Regulatory Complience
by Check the list of the documents of the respective department and identify the areas to be analyzed for gap, according to the criticality of the …
Category: Audit
Worst Case Identification in Cleaning Validation
Cleaning is a crucial step in the manufacturing of pharmaceutical products, and it is essential to validate that the equipment is cleaned thoroughly. In identifying …
SOP For Out of Calibration (OOC) of Laboratory Instruments
PURPOSE: To lay down a procedure for the handling out of calibration (OOC) results of Quality Control Laboratory Instruments and Equipment. SCOPE: This SOP …
Audit / Engineering / GMP / Microbiology / Production / Quality Assurance / Quality Control / SOPs / Store / Ware house / Uncategorized
SOP FOR HANDLING OF CHANGE CONTROL
OBJECTIVE To lay down a procedure to describe the handling of change control which include the procedure for initiation, evaluation, review, approval/ rejection of proposed …
Audit / Engineering / GMP / Microbiology / Quality Assurance / Quality Control / SOPs / Store / Ware house
SOP FOR HANDLING OF DEVIATION
OBJECTIVE To describe the procedure for handling of deviations. 2.0 SCOPE This SOP is applicable for any deviation in an established process in all …
Entry & Exit Procedure In Quality Control Lab.
OBJECTIVE:To lay down a procedure entry & exit procedure in QC Lab.SCOPE:This procedure is applicable for entry & exit procedure in QC Lab.RESPONSIBILITY:QC Officer/ QC …