Production - Pharma Egg

Mar12022 by KBS.No Comments

Training in Pharmaceuticals Industries

Production

In this post the complete detail is given about Training in Pharmaceuticals Industries, which help to personnel work-friendly in the pharmaceuticals industry. Training in Pharmaceuticals Industries OBJECTIVE 1.1. The purpose of this SOP is to describe the procedure for Training in Pharmaceuticals Industries of the personnel working under cGMP environment at Pharmaceutical. SCOPE 2.1. The scope of this Training in Pharmaceuticals Industries SOP pertains to all the persons working at Pharmaceutical. RESPONSIBILITY 3.1. It is the responsibility of departmental heads to follow this SOP as it is written. 3.2. It is the responsibility of QA to ensure that all employees have been trained and qualified in their respective job functions, regulatory and compliance procedures and safety regula...

Mar12022 by KBS.No Comments

Destruction Of Expired and Rejected Material

Production

Destruction Of Expired and Rejected Material SOP is described in this blogpost. PURPOSE: This procedure is established to destroy Expired Raw Materials, Expired & Rejected Returned Stock, Rejected In-process products, Rejected Packaging Components and obsolete records & documents. Responsibility: Warehouse Incharge, QC/QA Manager, Plant Manager and Chief Executive Officer. Procedure: Destruction is to be carried out semiannually preferably in the month of January & July of every year or when ever required. Segregate and Collected the Items as under:- 1. All rejected Raw Material (Active & non Active. 2. All Rejected inprocess products batches. 3. All Returned and Rejected Finished Stock from market & production. 4. All Rejected Packaging Components and o...

Mar12022 by KBS.No Comments

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...

Mar12022 by KBS.No Comments

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...

Mar12022 by KBS.No Comments

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 ...

Feb122022 by KBS.No Comments

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...

Feb122022 by KBS.No Comments

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...

Feb122022 by KBS.No Comments

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...

Feb122022 by KBS.No Comments

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...

Feb122022 by KBS.No Comments

Handling of Controlled Items in Production Area SOP

Production

Handling of Controlled Items in Production Area is prepared for the Production area of pharmaceuticals factory. Handling of Controlled Items in Production Area OBJECTIVE 1.1 To lay down the procedure for handling of controlled items in the production area. SCOPE 2.1 The scope of this SOP pertains to the handling of controlled items in the tablet section of the production area. RESPONSIBILITIES 3.1 It is the responsibility of Supervisor (Tablet) to follow this SOP as it is written. 3.2 It is the responsibility of Production Pharmacist (Tablet) to ensure that this procedure is followed in its entirety. 3.3 It is the responsibility of QAO to verify that this SOP is properly followed in its entirety. 3.4 It is the responsibility of Production Manager to make certain that thi...