Skip to content
  • Clinical Studies
  • Pharma GMP
  • Pharma Tips
  • Stability Studies
  • Pharma Books
  • Schedule M

SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

  • Home
  • Job Safety Analysis (JSA)
    • Oral Dosage Forms (Tablets & Capsules)
    • Oral Liquid Dosage Forms (Syrups, Elixirs, Suspensions, Emulsions)
    • Powder and Granule Dosage Forms
    • Topical Dosage Forms (Creams, Ointments, Gels, Lotions, Pastes)
    • Transdermal Dosage Forms (Patches)
  • Standard Test Procedures (STP)
  • SOP – Blog Post
  • Toggle search form

Tag: SOP for Equipment Validations

SOP for Qualification of Strip Packaging Machines

Posted on By

SOP for Qualification of Strip Packaging Machines Standard Operating Procedure for Qualification of Strip Packaging Machines 1) Purpose The purpose of this Standard Operating Procedure (SOP) is to define the process for qualifying strip packaging machines used in pharmaceutical manufacturing. This SOP ensures that the strip packaging machines are correctly installed, operate according to specifications,…

Read More “SOP for Qualification of Strip Packaging Machines” »

Validations and Qualifications

SOP for Qualification of Powder Sieving Machines

Posted on By

SOP for Qualification of Powder Sieving Machines Standard Operating Procedure for Qualification of Powder Sieving Machines 1) Purpose The purpose of this Standard Operating Procedure (SOP) is to define the process for qualifying powder sieving machines used in pharmaceutical manufacturing. This SOP ensures that the sieving machines are correctly installed, operate according to specifications, and…

Read More “SOP for Qualification of Powder Sieving Machines” »

Validations and Qualifications

SOP for Qualification of Tablet Dedusters

Posted on By

SOP for Qualification of Tablet Dedusters Standard Operating Procedure for Qualification of Tablet Dedusters 1) Purpose The purpose of this Standard Operating Procedure (SOP) is to define the process for qualifying tablet dedusters used in pharmaceutical manufacturing. This SOP ensures that tablet dedusters, which are used to remove excess powder from tablets after compression, are…

Read More “SOP for Qualification of Tablet Dedusters” »

Validations and Qualifications

SOP for IQ/OQ/PQ of Automatic Tablet Inspection Machines

Posted on By

SOP for IQ/OQ/PQ of Automatic Tablet Inspection Machines Standard Operating Procedure for IQ/OQ/PQ of Automatic Tablet Inspection Machines 1) Purpose The purpose of this Standard Operating Procedure (SOP) is to define the process for Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) of automatic tablet inspection machines used in pharmaceutical manufacturing. This SOP…

Read More “SOP for IQ/OQ/PQ of Automatic Tablet Inspection Machines” »

Validations and Qualifications

SOP for Qualification of Capsule Filling Machines

Posted on By

SOP for Qualification of Capsule Filling Machines Standard Operating Procedure for Qualification of Capsule Filling Machines 1) Purpose The purpose of this Standard Operating Procedure (SOP) is to define the process for qualifying capsule filling machines used in pharmaceutical manufacturing. This SOP ensures that the capsule filling machines are installed, operated, and perform consistently under…

Read More “SOP for Qualification of Capsule Filling Machines” »

Validations and Qualifications

SOP for Qualification of Granulators (High-Shear and Oscillating)

Posted on By

SOP for Qualification of Granulators (High-Shear and Oscillating) Standard Operating Procedure for Qualification of Granulators (High-Shear and Oscillating) 1) Purpose The purpose of this Standard Operating Procedure (SOP) is to define the process for qualifying high-shear and oscillating granulators used in pharmaceutical manufacturing. This SOP ensures that the granulators are installed, operate according to specifications,…

Read More “SOP for Qualification of Granulators (High-Shear and Oscillating)” »

Validations and Qualifications

SOP for IQ/OQ/PQ of Blenders (Ribbon, V-Blender)

Posted on By

SOP for IQ/OQ/PQ of Blenders (Ribbon, V-Blender) Standard Operating Procedure for IQ/OQ/PQ of Blenders (Ribbon, V-Blender) 1) Purpose The purpose of this Standard Operating Procedure (SOP) is to define the process for Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) of Ribbon and V-Blenders used in pharmaceutical manufacturing. This SOP ensures that the…

Read More “SOP for IQ/OQ/PQ of Blenders (Ribbon, V-Blender)” »

Validations and Qualifications

SOP for Performance Qualification (PQ) of Tablet Coating Machines

Posted on By

SOP for Performance Qualification (PQ) of Tablet Coating Machines Standard Operating Procedure for Performance Qualification (PQ) of Tablet Coating Machines 1) Purpose The purpose of this Standard Operating Procedure (SOP) is to define the process for performing Performance Qualification (PQ) of tablet coating machines in pharmaceutical manufacturing. This SOP ensures that the tablet coating machine…

Read More “SOP for Performance Qualification (PQ) of Tablet Coating Machines” »

Validations and Qualifications

SOP for Operational Qualification (OQ) of Fluidized Bed Dryers

Posted on By

SOP for Operational Qualification (OQ) of Fluidized Bed Dryers Standard Operating Procedure for Operational Qualification (OQ) of Fluidized Bed Dryers 1) Purpose The purpose of this Standard Operating Procedure (SOP) is to define the process for performing Operational Qualification (OQ) of fluidized bed dryers used in the pharmaceutical manufacturing process. This SOP ensures that the…

Read More “SOP for Operational Qualification (OQ) of Fluidized Bed Dryers” »

Validations and Qualifications

SOP for Installation Qualification (IQ) of Tablet Compression Machines

Posted on By

SOP for Installation Qualification (IQ) of Tablet Compression Machines Standard Operating Procedure for Installation Qualification (IQ) of Tablet Compression Machines 1) Purpose The purpose of this Standard Operating Procedure (SOP) is to define the process for performing Installation Qualification (IQ) for tablet compression machines in pharmaceutical manufacturing. This SOP ensures that the tablet compression machine…

Read More “SOP for Installation Qualification (IQ) of Tablet Compression Machines” »

Validations and Qualifications

Posts pagination

Previous 1 … 5 6 7 … 10 Next

Standard Operating Procedures V 1.0

  • Aerosols
  • Analytical Method Development
  • Bioequivalence Bioavailability Study
  • Capsule Formulation
  • Clinical Studies
  • Creams
  • Data Integrity
  • Dental Dosage Forms
  • Drug Discovery
  • Environment, Health and Safety
  • Formulation Development
  • Gels
  • Good Distribution Practice
  • Good Warehousing Practices
  • In-Process Control
  • Injectables
  • Liquid Orals
  • Liposome and Emulsion Formulations
  • Lotions
  • Lyophilized Products
  • Maintenance Dept.
  • Medical Devices
  • Metered-Dose Inhaler
  • Microbiology Testing
  • Nanoparticle Formulation
  • Nasal Spray Formulations
  • Nebulizers
  • Ocular (Eye) Dosage Forms
  • Ointments
  • Otic (Ear) Dosage Forms
  • Pharmacovigilance
  • Powder & Granules
  • Purchase Departments
  • Quality Assurance
  • Quality Control
  • Raw Material Stores
  • Regulatory Affairs
  • Tablet Manufacturing
  • Rectal Dosage Forms
  • Transdermal Patches
  • Vaginal Dosage Forms
  • Validations and Qualifications

Read SOPs in your Language:

English
 - 
en
Bengali
 - 
bn
English
 - 
en
Gujarati
 - 
gu
Hindi
 - 
hi
Malayalam
 - 
ml
Marathi
 - 
mr
Punjabi
 - 
pa
Tamil
 - 
ta
Telugu
 - 
te

NEW! Revised SOPs – V 2.0

  • Aerosols V 2.0
  • API Manufacturing V 2.0
  • BA-BE Studies V 2.0
  • Capsules V 2.0
  • Creams V 2.0
  • Ointments V 2.0
  • Raw Material Warehouse V 2.0
  • Tablet Manufacturing V2.0

New Publication: A must for All.

Copyright © 2025 SOP Guide for Pharma.

Powered by PressBook WordPress theme