SOP for cleaning of FBD bag Standard Operating Procedure (SOP) Objective To lay down a procedure for cleaning of FBD bags. Scope This SOP is applicable for the cleaning of FBD bags in the formulation plant. Responsibility Production Operator/ Technician – For cleaning of the equipment. Production Officer/ Executive – For checking the cleanliness of…
SOP for operation of Tablet Inspection Machine Standard Operating Procedure (SOP) Objective To lay down the procedure for operation of Tablet Inspection Machine. Scope This SOP is applicable for the operation of Tablet Inspection Machine in the formulation plant. Responsibility Production Operator/ Technician – For operation of the machine. Production Officer/ Executive – To maintain…
Read More “SOP for operation of Tablet Inspection Machine” »
SOP for operation of Auto coater Standard Operating Procedure (SOP) Objective To lay down a procedure for operation of Auto coater. Scope This SOP is applicable for operation of Auto coater in the formulation plant. Responsibility Production Operator/ Technician – For operation of the machine. Production Officer/Executive -To maintain proper functioning of the equipment &…
Document Management System in Quality Assurance Department Standard Operating Procedure (SOP) Objective: To lay down a procedure for Management of Documents in Quality Assurance Department in Pharma Industry Scope: Applicable for Document Management system in Quality Assurance department. Responsibility: Quality Assurance Department Accountability: Head- QA shall be accountable for compliance of this SOP. Procedure: Storage…
Read More “Document Management System in Quality Assurance Department in Pharma Industry” »
SOP for operation of rapid mixer granulator (RMG) with cone mill in Pharma Industry Standard Operating Procedure (SOP) Objective To lay down a procedure for operation of rapid mixer granulator with cone mill in Pharma Industry Scope This SOP is applicable for operation of rapid mixer granulator with cone mill to the formulation plant of Pharma…
Read More “SOP for operation of rapid mixer granulator (RMG) with cone mill in Pharma Industry” »
Cleaning of Rapid Mixer Granulator with Cone Mill in Pharma Industry Standard Operating Procedure (SOP) Objective: To lay down a procedure for cleaning of Rapid Mixer Granulator with cone mill in Pharma Industry. Scope: This SOP is applicable for the cleaning of Rapid Mixer Granulator with cone mill located in oral section at formulation plant…
Read More “Cleaning of Rapid Mixer Granulator with Cone Mill in Pharma Industry” »
SOP on cleaning of Paste Kettle in Pharma Industry Standard Operating Procedure (SOP) Objective To lay down a procedure for cleaning of Paste Kettle in Pharma Industry. Scope This SOP is applicable for the cleaning of Paste Kettle in the formulation plant of Pharma Industry. Responsibility Production Operator/ Technician – For cleaning of the equipment….
Read More “SOP on cleaning of Paste Kettle in Pharma Industry” »
SOP for operation of Metal Detector in Pharma Industry Standard Operating Procedure (SOP) Objective: To lay down a procedure for operation of metal detector in Pharma Industry. Scope: This SOP is applicable for the operation of metal detector to the formulation plant of Pharma Industry. Responsibility: Production Operator/ Technician shall be responsible for operation of the…
Read More “SOP for operation of Metal Detector in Pharma Industry” »
SOP on the operation of Paste Kettle In the Pharma Industry Objective To lay down the procedure for operation of Paste Kettle In Pharma Industry. Scope This SOP is applicable for operation of Paste Kettle In Pharma Industry. Responsibility Production Operator/ Technician – For operation of the equipment. Production Officer/ Executive – For checking the…
Read More “SOP on Operation of Paste Kettle In Pharma Industry” »
Contract production, analysis, and other activities in the Pharma Industry Principle. Contract production, analysis and any other activity covered by GMP must be correctly defined, agreed and controlled in order to avoid misunderstandings that could result in a product, or work or analysis, of unsatisfactory quality. All arrangements for contract production and analysis, including technology…
Pharma Manufacturing Premises – Risk classification guide for drug good manufacturing practices observations Risk 1 (critical) observations in Pharma Industry There was no air filtration system to eliminate airborne contaminants likely to be generated during fabrication or packaging. There was generalized malfunctioning of the ventilation system(s), with evidence of widespread cross-contamination. Segregation of manufacturing or…
Read More “Pharma Manufacturing Premises – Risk classification observations” »
