sop for cleaning validation in pharma 1.0 OBJECTIVE 1.1 The objective of this SOP is to define the procedure for cleaning validation. 2.0 SCOPE 2.1 This SOP is applicable for cleaning validation 3.0 RESPONSIBILITY 3.1 Executive –Quality Assurance – Prepare the SOP and follow-up the SOP accordingly. 3.2 Asst. Manager –Quality Assurance -Provide the support … Read more
sop for validation plan 1.0 OBJECTIVE 1.1 The objective of this SOP is to define the procedure for validation plan. 2.0 SCOPE 2.1 This SOP is applicable for validation plan 3.0 RESPONSIBILITY 3.1 Executive -Quality Assurance – Prepare the SOP and follow-up the SOP accordingly. 3.2 Asst. Manager –Quality Assurance -Provide the support to … Read more
sop for approval and release of finished products for market 1.0 OBJECTIVE 1.1 The objective of this SOP is to define the procedure for approval and release of finished product for market. 2.0 SCOPE 2.1 This SOP is applicable for approval and release of finish product for market 3.0 RESPONSIBILITY 3.1 Officer–Quality assurance-Prepare the … Read more
sop for preparation checking and approval of artwork 1.0 OBJECTIVE 1.1 The printed packaging material like labels, cartons, leaflet, insert etc having any text matter intended to be printed directly on the container, held extremely important position in pharmaceutical industry as they provide valuable information on identity, strength, dosage schedule and expiry of … Read more
sop for annual product quality review APQR 1.0 OBJECTIVE 1.1 The objective of this SOP is to define the procedure for procedure for prepare annual product quality review. 2.0 SCOPE 2.1 This SOP is applicable for prepare annual product quality review of finished product manufactured 3.0 RESPONSIBILITY 3.1 Officer –Quality Assurance – Prepare the … Read more
sop for status labeling of equipment and product 1.0 OBJECTIVE 1.1 The objective of this SOP is to define the procedure for define the procedure for status labeling procedure for equipment. 2.0 SCOPE 2.1 This SOP is applicable for Status Labeling Procedure of Equipment 3.0 RESPONSIBILITY 3.1 Executive/Officer –Concerned Department/Quality Assurance 4.0 ACCOUNTABILITY 4.1 … Read more
sop for standard batch size 1.0 OBJECTIVE 1.1 The objective of this SOP is to standardize the batch size of products. 2.0 SCOPE 2.1 This SOP is applicable for standardizing the batch size of Injectable products manufacturing 3.0 RESPONSIBILITY 3.1 Asst. Officer or above –Quality assurance – Prepare the SOP and follow-up the SOP accordingly … Read more
sop for equipment log card 1.0 OBJECTIVE 1.1 The objective of this SOP is to define the procedure for recording the operation cleaning and maintenance related machine utilization details of all the individual equipment. 2.0 SCOPE 2.1 This SOP is applicable for operation, cleaning and maintenance related machine utilization details of all the individual equipment … Read more
sop for document equipment numbering system 1.0 OBJECTIVE 1.1 The objective of this SOP is to define the procedure for numbering of documents / existing & new equipment & facilities in different functional areas. 2.0 SCOPE 2.1 This SOP is applicable for numbering of documents/ existing equipments and new equipments & facility in different functional … Read more
sop for conditional release in pharma 1.0 OBJECTIVE 1.1 The objective of this SOP is to define the procedure for conditional release of raw materials and finished products. 2.0 SCOPE 2.1 This SOP is applicable for conditional release of raw materials and finished products 3.0 RESPONSIBILITY 3.1 Officer-Quality Assurance – Prepare the SOP and follow-up … Read more