0.01 M Sodium Tetraphenylborate Preparation and Standardization

by
0.01 M Sodium Tetraphenylborate Preparation and Standardization

Preparation and Standardization of 0.01 M Sodium Tetraphenylborate (C6H5)4BNa) solution and calculating formula in Pharmaceutical labs. Name: 0.01 M Sodium Tetraphenylborate (C6H5)4BNa) Reagents: Sodium TetraphenylborateSodium HydroxideAluminium HydroxideSodium ChlorideCetylpyridinium ChloridePotassium Chloride Method of Preparation: Method of Standardization: Calculation: The calculation formula is : Where ‘a’ is the volume of 0.005 M cetylpyridinium chloride required without potassium … Read more

0.1 M Tetrabutylammonium Hydroxide Solution Preparation and Standardization

by
0.1 M Tetrabutylammonium Hydroxide Solution

Preparation and Standardization of 0.1 M Tetrabutylammonium Hydroxide (C16H37NO) Solution in Pharmaceutical Labs. Name: 0.1 M Tetrabutylammonium Hydroxide (C16H37NO) Reagents : Preparation of 0.1 M Tetrabutylammonium Hydroxide: Method of Standardization: Storage: Store below 25°C & store in an amber-colored bottle. Protect exposure from CO2 & water. Shelf life: The shelf life of the above solution … Read more

Technology Transfer Checklist For Sending Plant

by

When the process of moving technology including (Chemicals, Production/ Manufacturing, Control, and drug product-related documents) from one place to another, so we can make the same good stuff every time, that’s called technology transfer. Below is the full Checklist of Technology Transfer For Sending the Plant. Project identification No. — Name of Product — Technology … Read more

Understanding Temperature Mapping of Storage Areas: Procedure and Guidelines

by
Temperature Mapping of Storage Area

Learn about Temperature Mapping of Storage Areas their Objective, Frequency, methodology, protocol, significance, Procedure, and Guidelines. Definition and significance: Definition: temperature mapping is a study in which it is ensured that the environmental condition of the studied area is uniform and well within the acceptance criteria Objectives: The objective of Temperature Mapping is to provide … Read more

SOP on Reference Standards and impurities

by
SOP on Reference Standards and impurities

Standard Operating Procedure on Procurement, Storage, Usage, and Destruction of Reference Standards and Impurities. In this SOP you will learn about the following: Related SOP: SOP on Withdrawal, Storage, Observation & Destruction of Control Sample 1.0 Objective: 1.1 To lay down a procedure for the Procurement, Storage, Usage, and Destruction of Reference Standards and impurities.2.0 … Read more

SOP on Working Standards- Preparation, Qualification, Usage, Storage, and Destruction

by
SOP on Working Standards

Standard operating procedure on Preparation, Qualification, Usage, Storage, and Destruction of Working Standards in Pharmaceutical Labs. Working standard SOP will cover the following points: 1.0 Objective: 1.1 To lay down a procedure for the Preparation, Qualification, Usage, Storage, and Destruction of Working Standards.2.0 Scope: 2.1. This procedure applies to the Preparation, Qualification, Usage, Storage, and … Read more

SOP on Operation of Fume Hood

by
SOP on Operation of Fume Hood

Standard operating procedure on Operation of Fume Hood and the Precaution to be taken before its operation. 1.0 Purpose: For proper handling of the instrument and to save the environment of the QC laboratory from hazards and corrosive chemicals in the laboratory. 2.0 Scope: This SOP is applicable to all hazards, volatile and corrosive chemicals … Read more

SOP on Procurement, Usage, and Storage of Primary Standards

by
SOP on Procurement, Usage, and Storage of Primary Standards

Standard Operating procedure on Procurement, Usage, and Storage of Primary Standards in Pharmaceutical Quality control Department. 1.0 Objective: 1.1 To lay down a procedure for Procurement, usage, and storage of primary standards 2.0 Scope: 2.1 This procedure is applicable for the Procurement, usage, and storage of primary standards being used in the Quality Control Department … Read more

SOP on intimation to QC Department for Retesting of Raw Materials

by
SOP on intimation to QC Department for Retesting of Raw Materials

Standard operating procedure on intimation to QC Department for Retesting of Raw Materials 1.0 Objective: To lay down the procedure for intimation to the QC Department for Retesting of Raw Materials2.0 Aim: This procedure applies to the Warehouse department in the pharmaceutical industry.3.0 Responsibility: 3.1 Raw material warehouse personnel to follow the procedure.3.2 Q.C. officer … Read more

Difference Between Endotoxins and Exotoxins

by
Difference Between Endotoxins and Exotoxins

Here, Let’s understand the Key Difference Between Endotoxins and Exotoxins. Endotoxins are biological toxins associated with the outer cell wall membrane of gram-negative bacteria such as E.coli, Salmonella, Shigella, Pseudomonas, vibrio cholera, etc. (Endotoxins are invariably associated with gram-negative bacteria whether the organisms are pathogenic or not). Endotoxins cause big reactions in our bodies, like … Read more

SOP for Operation and Calibration of Flame Photometer

by
SOP for Operation and Calibration of Flame Photometer

Standard operating procedure for Operation and Calibration of Flame Photometer 1.0 Objective: To lay down the procedure for the operation and calibration of the Flame photometer.2.0 Scope: This procedure applies to Flame Photometer instrument installed in the Quality Control Department in Pharmaceutical.3.0 Responsibility: Officer/ Execution responsible for the implementation of this procedure.QC Asst. Manager/ Manager … Read more

SOP for Operation of Digital Griffin Flask Shaker

by
Digital Griffin Flask Shaker

Standard Operating Procedure for Operation of Digital Griffin Flask Shaker 1.0 Objective: To provide a procedure for operating the digital Griffin flask shaker. 2.0 Scope: The procedure shall be applied when operating the digital Griffin flask shaker in the Q.C Laboratory. 3.0 Responsibility: QC Executive and any personnel using the equipment to follow the outlined … Read more

Silica Based Column Cleaning, Regeneration and Storage

by
Silica Based Column Cleaning, Regeneration and Storage

Column Cleaning, Regeneration, and Storage of Silica Based Columns are necessary to prevent unnecessary problems during the Process. So when you’re using those in-line filters or guard cartridges for your HPLC columns, it’s like giving them armor against getting clogged or stuff sticking to them. But you know what? Even with these guard things, over … Read more

SOP on Temperature Mapping in RM, PM, FG and Control Sample Area

by

Standard Operating procedure on SOP on Temperature Mapping in RM, PM, FG, and Control sample Area 1.0 Objective: To Lay down the Procedure for Temperature Mapping in PM, RM, FG, and Control Sample area (Storage Area).2.0 Scope: 2.1 This SOP shall apply to all storage areas in Pharmaceutical industries.3.0 Reference: In –House 4.0 Responsibility:4.1 RM, … Read more

SOP on Preventive Maintenance of Auto Coater Machine

by
SOP on Preventive Maintenance of Auto Coater Machine

Learn about Standard operating procedures on Preventive Maintenance of Auto Coater machines in Pharmaceutical industries. 1.0 Objective: To lay down a procedure for Preventive Maintenance of Auto Coater. 2.0 Responsibility: 2.1 Operator, and Officer to perform the preventive maintenance activities as per the respective SOP.2.2 Executives (Eng.Dept.) to prepare and comply with the preventive maintenance … Read more