SOP for Quality Management Review (QMR)
Quality Management Review (QMR) 1.0 OBJECTIVETo lay down the procedure for to ensure that the objective &effectiveness of the quality […]
Quality Management Review (QMR) 1.0 OBJECTIVETo lay down the procedure for to ensure that the objective &effectiveness of the quality […]
Handling of Product Failure 1.0 OBJECTIVETo lay down the procedure for investigation on Handling of Product Failure of any batch.2.0
Handling of Returned Product 1.0 OBJECTIVETo lay down the procedure for handling of returned drug product in quality assurance department.
Good Documentation Practices (GDP) 1.0 OBJECTIVETo lay down the procedure for good documentation practices for GxP documents (electronic records and
Handling of Deviation 1.0 OBJECTIVETo lay down the procedure for handling of deviation In Quality assurance department. 2.0 SCOPE2.1 This
Handling of Swab Sampling 1.0 OBJECTIVETo lay down the procedure for swab sampling of equipment. 2.0 SCOPEThis procedure is applicable
Handling of Technology Transfer 1.0 OBJECTIVETo lay down the procedure for technology transfer (TT) of new products intended to be
Line Clearance 1.0 OBJECTIVETo lay down the procedure to ensure that the area and equipment, required for the dispensing, manufacturing
Responsibility of IPQA Personnel 1.0 OBJECTIVETo lay down the procedure for the responsibilities of IPQA personnel in sterile dry powders,
Starting Material Non-Conformance/Discrepancy Intimation 1.0 OBJECTIVETo lay down the procedure to communicate the vendor in case of non-conformance/discrepancy observed in