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Returned Goods Handling

Production
Returned Goods Handling is described in this blogpost that help to handle of return goods OBJECTIVE: To describe the procedure for returned goods received from distributors/market. PROCEDURE: i) Returned goods received from Distributors will be received on a document. ii) This stock will be sorted out and segregated into 4 categories Category No.1 Stock can be reused if having reasonable shelf life at least more than six months after checking from Q.C. and redressing if required. Category No.2 If left over shelf life is between 3-6 months it will be converted to Physician sample after Q.C. checking. Category No.3 If the shelf life is below three months, it can be donated to any running clinic, or charity organization after checking from Q.C. and redressing if required, with fina...

Retaining Of Sample Of Finished Goods

Production
In this blog we come to know how to retaining of sample of finished Goods in pharmaceuticals industry. Retaining Of Sample Of Finished GoodsOBJECTIVE 1.1 To lay down the procedure for retaining of sample. SCOPE 2.1 The scope of this SOP applies to the procedure for retaining of sample of a product from packing line in packaging section of production department. RESPONSIBILITIES 3.1 It is the responsibility of Line Supervisors (packaging) to follow this SOP as it is written. 3.2 It is the responsibility of Production Pharmacist (packaging) to ensure that this SOP is followed as it is written. 3.3 It is the responsibility of Production Manager to ensure that this SOP is followed in its entirety, reviewed and updated as necessary. DEFINITIONS & ABBREVIATIONS 4.1 SOP: Standar...

Batch Stamp Preparation SOP in Pharma

Production
In pharmaceutical industry Batch Stamp Preparation SOP is used for printing on unit carton, label etc Batch Stamp Preparation OBJECTIVE 1.1 To lay down the procedure for making batch stamp. SCOPE 2.1 The scope of this SOP pertains to procedure for making batch stamp. RESPONSIBILITIES 3.1 It is the responsibility of Production Pharmacist (packing) to ensure that this SOP is followed as it is written. 3.2 It is the responsibility of Production Manager, to ensure that this SOP is followed in its entirety, reviewed and update as necessary. DEFINITIONS & ABBREVIATIONS 4.1 SOP: Standard Operating Procedure 4.2 BPR: Batch Processing Record MATERIALS & EQUIPMENTS NA PROCEDURES 6.1 Confirm batch number from batch order. 6.2 Confirm manufacturing date from final release ...
Dextromethorphan Hydrobromide Raw Material Testing

Dextromethorphan Hydrobromide Raw Material Testing

Testing Methods, Raw Material
Dextromethorphan Hydrobromide Raw Material Testing specification & analysis prescribes the requirements with IR spectrum and Alternate Method of Analysis on UV System and Other Testing procedures. Dextromethorphan Hydrobromide Raw Material Testing PURPOSE This raw material specification & analysis prescribes the requirements Dextromethorphan Hydrobromide Raw Material Testing which is used in Syrup & Tablet. 1.0 PURPOSE This raw material specification & analysis prescribes the requirements for Dextromethorphan Hydrobromide which is one of the components of Syrup & Tablet. 2.0 SCOPE It is applicable in Material Department, Product Development and Quality Assurance Department to confirm its physical and chemical specifications. 3.0 REFERENCES USP/BP 4.0 DE...
Deionized Water Testing Procedure

Deionized Water Testing Procedure

Testing Methods, Raw Material
Deionized Water Testing Procedure Raw Material specification & analysis prescribes the requirements with and Other Testing procedures. Deionized Water Testing Procedure for Raw Material PURPOSE Deionized Water Testing Procedure PURPOSE This raw material specification & analysis prescribes the requirements for De-ionized water, which is used in different pharmaceutical preparations. SCOPE It is applicable for the analysis of Do-ionized water manufactured in water treatment section. REFERENCES In-house DEFINITIONS Follow SOP determination Pharmaegg.com SPECIFICATIONS In-house PHYSICAL ANALYSIS TESTS SPECIFICATIONS 1. Physical Form Liquid 2. Colour Colourless 3. pH Between 5.0 to 7.0 at 30°C 4. Conductivity Should not be more than 1.4µS/cm at 30°C CHEMICAL ANALYSIS ...
How to Test Cloxacillin Sodium

How to Test Cloxacillin Sodium

General Topics, Raw Material, Testing Methods
How To Test Cloxacillin Sodium Raw Material specification & analysis prescribes the requirements with IR spectrum and Alternate Method of Analysis on HPLC System and Other Testing procedures. How To Test Cloxacillin Sodium Raw Material PURPOSE This raw material specification & analysis prescribes the requirements for How To Test Cloxacillin Sodium Raw Material which is used in Capsules. PURPOSE This raw material specification & analysis prescribes the requirements for Cloxacillin Sodium (Compacted) which is one of the component of Capsule. SCOPE It is applicable in Material Department, Product Development and Quality Assurance Department to confirm its physical and chemical specifications. REFERENCES USP/BP/Inhouse DEFINITIONS Follow SOP pharmaegg.co...
Assigning Work To Various Workers On A Line For Packaging

Assigning Work To Various Workers On A Line For Packaging

Production
Assigning Work To Various Workers On A Line For Packaging SOP is created for the Production area of pharmaceuticals. Assigning Work To Various Workers On A Line For Packaging OBJECTIVE 1.1 To assign the work to various workers on a line for packaging. SCOPE 2.1 The scope of this SOP applies to assign work to various workers on a packing line in packaging section of production department. RESPONSIBILITIES 3.1 It is the responsibility of packing line Supervisor (packaging) to follow this SOP as it is written. 3.2 It is the responsibility of Production Pharmacist (packaging) to ensure that this SOP is followed as it is written. 3.3 It is the responsibility of Production Manager, to ensure that this SOP is followed in its entirety, reviewed and update as necessary. DEFINITIONS...
Packing Of Tablets And Capsules In Packaging Section

Packing Of Tablets And Capsules In Packaging Section

Production
In this post completely explained about Packing Of Tablets And Capsules In Packaging Section in pharma. Packing Of Tablets And Capsules In Packaging Section OBJECTIVE 1.1 To describe the procedure for packing of tablets and capsules in packaging section. SCOPE 2.1 The scope of this SOP applies to packaging of tablets and capsules in packaging section of production department. RESPONSIBILITIES 3.1 It is the responsibility of Line Supervisor (packaging) to follow this Packing Of Tablets And Capsules In Packaging Section SOP as it is written. 3.2 It is the responsibility of Packaging Pharmacist to ensure that this Packing Of Tablets And Capsules In Packaging Section SOP is followed as it is written. 3.3 It is the responsibility of Production Manager, to ensure that this SOP is...
Packing of Products on a Packaging Line SOP

Packing of Products on a Packaging Line SOP

Production
In this SOP the complete procedure of Packing of Products on a Packaging Line is described which is applied in the pharmaceuticals production section. Packing of Products on a Packaging Line OBJECTIVE 1.1 To lay down the procedure for packing of a product on a packaging line. SCOPE 2.1 The scope of this SOP applies to the procedure for packing of a product on packaging line in packaging section of production department. 3.0 RESPONSIBILITIES 3.1 It is the responsibility of Line Supervisor (packaging) to follow this SOP as it is written. 3.2 It is the responsibility of Packaging Pharmacist to ensure that this SOP is followed as it is written. 3.3 It is the responsibility of Production Manager to ensure that this SOP is followed in its entirety, reviewed and updated as necessa...

General Cleanliness In Packaging Section SOP

Production
This is SOP of General Cleanliness In Packaging Section of pharmaceuticals industry which applied for cleaning. General Cleanliness In Packaging Section OBJECTIVE 1.1 To lay down the procedure for general cleanliness in packaging section. SCOPE 2.1 The scope of this SOP pertains to general cleanliness in packaging section of production department. RESPONSIBILITIES 3.1 It is the responsibility of Supervisor (packaging) to follow this SOP as it is written. 3.2 It is the responsibility of Production Pharmacist (packaging) to ensure that this SOP is followed as it is written. 3.3 It is the responsibility of Production Manager, to ensure that this SOP is followed in its entirety, reviewed and updated as necessary. 4.0 DEFINITIONS & ABBREVIATIONS 4.1 SOP: Standard Operating...