Tag: Viscosity testing for injections

Injectables: SOP for Change Control Management

SOP for Change Control Management Standard Operating Procedure for Change Control Management 1) Purpose The purpose of this Standard Operating Procedure (SOP) is to establish procedures for initiating, documenting, reviewing, approving, and implementing changes within the pharmaceutical manufacturing facility to ensure compliance with regulatory requirements, maintain product quality, and manage risks effectively. 2) Scope This…

Injectables

SOP for Validation of Analytical Methods

SOP for Validation of Analytical Methods Standard Operating Procedure for Validation of Analytical Methods 1) Purpose The purpose of this Standard Operating Procedure (SOP) is to establish procedures for the validation of analytical methods used for testing pharmaceutical raw materials, intermediates, and finished products to ensure accuracy, reliability, and compliance with regulatory requirements. 2) Scope…

Injectables

SOP for Cleaning and Sanitization of Manufacturing Equipment

SOP for Cleaning and Sanitization of Manufacturing Equipment Standard Operating Procedure for Cleaning and Sanitization of Manufacturing Equipment 1) Purpose The purpose of this Standard Operating Procedure (SOP) is to establish procedures for the cleaning and sanitization of manufacturing equipment used in pharmaceutical production to prevent cross-contamination, ensure product quality, and comply with regulatory requirements….

Injectables

SOP for Handling and Storage of Controlled Substances

SOP for Handling and Storage of Controlled Substances Standard Operating Procedure for Handling and Storage of Controlled Substances 1) Purpose The purpose of this Standard Operating Procedure (SOP) is to establish procedures for the safe handling, storage, distribution, and disposal of controlled substances within the pharmaceutical manufacturing facility to prevent diversion, misuse, and ensure compliance…

Injectables

SOP for Managing and Archiving Batch Records

SOP for Managing and Archiving Batch Records Standard Operating Procedure for Managing and Archiving Batch Records 1) Purpose The purpose of this Standard Operating Procedure (SOP) is to establish procedures for the management, review, approval, and archival of batch records generated during pharmaceutical manufacturing processes to ensure compliance with regulatory requirements and product quality standards….

Injectables

SOP for Process Analytical Technology (PAT) Implementation

SOP for Process Analytical Technology (PAT) Implementation Standard Operating Procedure for Process Analytical Technology (PAT) Implementation 1) Purpose The purpose of this Standard Operating Procedure (SOP) is to establish procedures for the implementation of Process Analytical Technology (PAT) in pharmaceutical manufacturing processes to enhance process understanding, control, and efficiency. 2) Scope This SOP applies to…

Injectables

SOP for IT Systems Validation and Data Integrity

SOP for IT Systems Validation and Data Integrity Standard Operating Procedure for IT Systems Validation and Data Integrity 1) Purpose The purpose of this Standard Operating Procedure (SOP) is to establish procedures for the validation and maintenance of information technology (IT) systems used in pharmaceutical manufacturing to ensure data integrity, system reliability, and compliance with…

Injectables

SOP for Requalification of Equipment and Systems

SOP for Requalification of Equipment and Systems Standard Operating Procedure for Requalification of Equipment and Systems 1) Purpose The purpose of this Standard Operating Procedure (SOP) is to establish procedures for the requalification of equipment, utilities, facilities, and systems within the pharmaceutical manufacturing facility to ensure continued compliance with regulatory requirements and consistent product quality….

Injectables

Injectables: SOP for Requalification of Equipment and Systems

Injectables

SOP for Validation Master Plan Preparation and Approval

SOP for Validation Master Plan Preparation and Approval Standard Operating Procedure for Validation Master Plan Preparation and Approval 1) Purpose The purpose of this Standard Operating Procedure (SOP) is to establish procedures for the preparation, approval, and maintenance of a Validation Master Plan (VMP) to ensure that all validation activities within the pharmaceutical manufacturing facility…

Injectables