Author: Auditor

SOP for Conducting Spray Drying for Formulation Screening

SOP for Conducting Spray Drying for Formulation Screening Standard Operating Procedure (SOP) for Conducting Spray Drying for Formulation Screening 1) Purpose The purpose of this Standard Operating Procedure (SOP) is to outline the process for conducting spray drying in the screening of pharmaceutical formulations. Spray drying is a critical technique used in the preparation of…

Drug Discovery

Ointments: SOP for Particle Size Analysis in Ointments – V 2.0

SOP for Particle Size Analysis in Ointments – V 2.0 Procedure for Particle Size Analysis in Ointments Department Quality Control (QC)/Quality Assurance (QA)/Analytical Development SOP No. SOP/Ointment/066 Supersedes V 1.0 Page No. Page X of Y Issue Date [Insert Issue Date] Effective Date [Insert Effective Date] Review Date [Insert Review Date] 1. Purpose The purpose…

Ointments V 2.0

Tablets: SOP for Using Automated Spray Coating Systems – V 2.0

Tablets: SOP for Using Automated Spray Coating Systems – V 2.0 Standard Operating Procedure for Using Automated Spray Coating Systems Department Tablet SOP No. SOP/TAB/066/2025 Supersedes SOP/TAB/066/2022 Page No. Page 1 of 6 Issue Date 10/01/2026 Effective Date 15/01/2026 Review Date 10/01/2027 1. Purpose To provide guidelines for the use of automated spray coating systems…

Tablet Manufacturing V2.0

Aerosol: SOP for Verifying Weighed Quantities of Raw Materials – V 2.0

Aerosol: SOP for Verifying Weighed Quantities of Raw Materials – V 2.0 SOP for Verifying Weighed Quantities of Raw Materials Department Aerosol SOP No. SOP/Aerosol/006/2025 Supersedes SOP/Aerosol/006/2022 Page No. Page 1 of Y Issue Date 06/02/2025 Effective Date 16/02/2025 Review Date 06/02/2028 1. Purpose This Standard Operating Procedure (SOP) outlines the process for verifying the…

Aerosols V 2.0

SOP for Rheological Studies in Formulation Screening

SOP for Rheological Studies in Formulation Screening Standard Operating Procedure (SOP) for Rheological Studies in Formulation Screening 1) Purpose The purpose of this Standard Operating Procedure (SOP) is to define the procedure for conducting rheological studies during the screening of pharmaceutical formulations. Rheological studies are critical for understanding the flow, viscosity, and shear stress characteristics…

Drug Discovery

SOP for Verification and Compliance of Storage Conditions Before Receipt – V 2.0

SOP for Verification and Compliance of Storage Conditions Before Receipt – V 2.0 Standard Operating Procedure for Verification and Compliance of Storage Conditions Before Receipt Department Warehouse / Quality Assurance / Quality Control / Procurement SOP No. SOP/RM/054/2025 Supersedes SOP/RM/054/2022 Page No. Page 1 of 15 Issue Date 01/02/2025 Effective Date 05/02/2025 Review Date 01/02/2026…

Raw Material Warehouse V 2.0

Ointments: SOP for Visual Inspection of Ointments – V 2.0

SOP for Visual Inspection of Ointments – V 2.0 Procedure for Visual Inspection of Ointments Department Quality Control (QC)/Quality Assurance (QA)/Production SOP No. SOP/Ointment/065 Supersedes V 1.0 Page No. Page X of Y Issue Date [Insert Issue Date] Effective Date [Insert Effective Date] Review Date [Insert Review Date] 1. Purpose The purpose of this Standard…

Ointments V 2.0

Tablets: SOP for Multi-Layer Tablet Manufacturing Process – V 2.0

Tablets: SOP for Multi-Layer Tablet Manufacturing Process – V 2.0 Standard Operating Procedure for Multi-Layer Tablet Manufacturing Process Department Tablet SOP No. SOP/TAB/065/2025 Supersedes SOP/TAB/065/2022 Page No. Page 1 of 6 Issue Date 05/01/2026 Effective Date 10/01/2026 Review Date 05/01/2027 1. Purpose To define the procedure for manufacturing multi-layer tablets, ensuring proper layer formation, uniformity,…

Tablet Manufacturing V2.0

SOP for Assessing Mechanical Properties of Formulations

SOP for Assessing Mechanical Properties of Formulations Standard Operating Procedure (SOP) for Assessing Mechanical Properties of Formulations 1) Purpose The purpose of this Standard Operating Procedure (SOP) is to establish the process for assessing the mechanical properties of pharmaceutical formulations, particularly solid dosage forms such as tablets, capsules, and granules. Mechanical properties, including hardness, friability,…

Drug Discovery

Ointments: SOP for Identifying Active Ingredient Potency in Ointments – V 2.0

SOP for Identifying Active Ingredient Potency in Ointments – V 2.0 Procedure for Identifying Active Ingredient Potency in Ointments Department Quality Control (QC)/Quality Assurance (QA)/Analytical Development SOP No. SOP/Ointment/064 Supersedes V 1.0 Page No. Page X of Y Issue Date [Insert Issue Date] Effective Date [Insert Effective Date] Review Date [Insert Review Date] 1. Purpose…

Ointments V 2.0