sop for handling of rejected material in pharma 1.0 OBJECTIVE 1.1 The objective of this SOP is to define the procedure for handling of rejected/expired material. 2.0 SCOPE 2.1 This SOP is applicable for handling of rejected/expired material 3.0 RESPONSIBILITY 3.1 Asst. Officer or above–Quality assurance-Prepare the SOP and follow-up the SOP accordingly 3.2 … Read more
sop for online rejection in pharma 1.0 OBJECTIVE 1.1 The objective of this SOP is to define the procedure for online rejection. 2.0 SCOPE 2.1 This SOP is applicable for online rejection of raw material/packing material/finished goods during complete processing of any batch 3.0 RESPONSIBILITY 3.1 Officer-Quality Assurance – Prepare the SOP and follow-up … Read more
sop for handling of returned goods 1.0 OBJECTIVE 1.1 The objective of this SOP is to define the procedure for handling of returned goods. 2.0 SCOPE 2.1 This SOP is applicable for handling of returned goods 3.0 RESPONSIBILITY 3.1 Officer –Quality assurance-Prepare the SOP and follow-up the SOP accordingly 3.2 Asst. manager –Quality assurance … Read more
sop for mock recall in pharma 1.0 OBJECTIVE 1.1 The objective of this SOP is to define the procedure of mock recall to evaluate the effectiveness of the arrangements of recall procedure. 2.0 SCOPE 2.1 This SOP is applicable to finished products to mock recall which were manufactured 2.1 Procedure for mock recall for domestic … Read more
sop for product recall in pharma 1.0 OBJECTIVE 1.1 The objective of this SOP is to define the procedure of recall of marketed product. 2.0 SCOPE 2.1 This SOP is applicable to finished products to be recalled which were manufactured and distributed in: 2.1.1 Domestic market through distributors (C&F), stockiest, retailers and marketing managers … Read more
sop for handling of market complaint in pharma 1.0 OBJECTIVE 1.1 The objective of this SOP is to define the procedure for errors and other unpredictable events can result in defective or unsafe products being released for distribution, with the potential for such goods to cause harm to the people who use them. This … Read more
sop for handling of out of specification results OOS 1.0 OBJECTIVE 1.1 The objective of this SOP is to define the procedure for handling of out of specification results (OOS) generated during the testing of Raw material, packing material, In-process samples, finished product samples and stability samples. 2.0 SCOPE 2.1 This SOP is applicable … Read more
sop for control sample management 1.0 OBJECTIVE 1.1 The objective of this SOP is to define the procedure for the collection, storage, periodical inspection, and destruction of control samples & to maintain the relevant Records. 2.0 SCOPE 2.1 This SOP is applicable for collection, storage, periodical inspection, and destruction of control samples & to … Read more
sop for prevention of cross contamination 1.0 OBJECTIVE 1.1 The objective of this SOP is to define the procedure for checks follows for prevention of cross contamination. 2.0 SCOPE 2.1 This SOP is applicable for various system controls to prevent cross contamination in manufacturing and packing area in factory premises 3.0 RESPONSIBILITY 3.1 Asst. … Read more
sop for entry of authorized person 1.0 OBJECTIVE 1.1 The objective of this SOP is to define the procedure for entry of authorized person. 2.0 SCOPE 2.1 This SOP is applicable for entry of authorized person in concerned department 3.0 RESPONSIBILITY 3.1 Asst. Officer or above-Quality Assurance – Prepare the SOP and follow-up the … Read more