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

SOPs for Tablet Manufacturing

Standard Operating Procedures (SOPs) play a crucial role in ensuring the quality, safety, and efficiency of pharmaceutical manufacturing processes. In the tablet department of a pharmaceutical company, SOPs are essential for maintaining consistency, accuracy, and compliance throughout the production of tablets. These SOPs outline the step-by-step procedures, responsibilities, and guidelines to be followed by personnel involved in various aspects of tablet production, including formulation, blending, compression, coating, packaging, and quality control. By adhering to well-defined SOPs, the tablet department can ensure the production of high-quality tablets that meet regulatory requirements and industry standards. SOPs provide clear instructions, minimize errors, promote uniformity, and enhance the overall quality assurance system within the tablet manufacturing process. They serve as valuable references for training, audits, and continuous improvement initiatives.

List of SOPs for Tablet Department:

Quality Control, Tablet Manufacturing: SOP for Tablet Friability Testing

Posted on By

Standard Operating Procedure for Tablet Friability Testing Purpose The purpose of this SOP is to provide detailed guidelines for conducting tablet friability testing in pharmaceutical manufacturing. Friability testing is a critical quality control parameter that assesses the ability of tablets to withstand abrasion and impacts during handling and transportation. This SOP ensures accurate and consistent…

Read More “Quality Control, Tablet Manufacturing: SOP for Tablet Friability Testing” »

Quality Control, Tablet Manufacturing

SOP for Operation of Tablet Friability Tester

Posted on By

Standard Operating Procedure for Operation of Tablet Friability Tester Purpose The purpose of this SOP is to establish clear guidelines for the proper operation of the tablet friability tester in pharmaceutical manufacturing. Friability testing is a critical quality control test that measures the resistance of tablets to abrasion and impacts during handling and transportation. This…

Read More “SOP for Operation of Tablet Friability Tester” »

Tablet Manufacturing

SOP for Handling and Maintenance of Hardness Testing Equipment

Posted on By

Standard Operating Procedure for Handling and Maintenance of Hardness Testing Equipment Purpose The purpose of this SOP is to provide comprehensive guidelines for the proper handling and maintenance of hardness testing equipment in pharmaceutical manufacturing. It ensures accurate and reliable hardness measurements, extends the life of the equipment, and maintains compliance with regulatory standards. Scope…

Read More “SOP for Handling and Maintenance of Hardness Testing Equipment” »

Tablet Manufacturing

SOP for Calibration and Verification of Hardness Tester

Posted on By

Standard Operating Procedure for Calibration & Verification of Hardness Tester: Purpose The purpose of this SOP is to provide detailed guidelines for the calibration and verification of the hardness tester in pharmaceutical manufacturing. Calibration and verification ensure the accuracy and reliability of hardness measurements, ensuring compliance with regulatory requirements and maintaining the highest standards of…

Read More “SOP for Calibration and Verification of Hardness Tester” »

Tablet Manufacturing

Tablet Manufacturing: SOP for Tablet Hardness Testing

Posted on By

Standard Operating Procedure for Tablet Hardness Testing Purpose The purpose of this SOP is to provide clear guidelines for the accurate and consistent measurement of tablet hardness in pharmaceutical manufacturing. Tablet hardness testing is a critical quality control parameter that ensures the tablets meet the required specifications and maintain their structural integrity during handling, transportation,…

Read More “Tablet Manufacturing: SOP for Tablet Hardness Testing” »

Tablet Manufacturing

SOP for Operation of Tablet Hardness Tester

Posted on By

Standard Operating Procedure for Operation of Tablet Hardness Tester Purpose The purpose of this SOP is to provide comprehensive guidelines for the proper operation of the tablet hardness tester in pharmaceutical manufacturing. It ensures accurate and consistent measurement of tablet hardness, which is a critical quality parameter for tablet production. Scope This SOP applies to…

Read More “SOP for Operation of Tablet Hardness Tester” »

Tablet Manufacturing

SOP for Deduster Screen Replacement and Calibration

Posted on By

Standard Operating Procedure (SOP) for Deduster Screen Replacement and Calibration Purpose The purpose of this SOP is to provide guidelines for the proper replacement and calibration of screens used in the tablet deduster. It ensures accurate particle separation, effective dedusting, and maintains the quality and integrity of the tablets during the manufacturing process. Scope This…

Read More “SOP for Deduster Screen Replacement and Calibration” »

Tablet Manufacturing

SOP for Cleaning and Maintenance of Tablet Deduster

Posted on By

Standard Operating Procedure (SOP) for Cleaning and Maintenance of Tablet Deduster Purpose The purpose of this SOP is to provide guidelines for the effective cleaning and maintenance of the tablet deduster in pharmaceutical manufacturing. It ensures the optimal performance of the equipment, minimizes the risk of cross-contamination, and maintains product quality and compliance with regulatory…

Read More “SOP for Cleaning and Maintenance of Tablet Deduster” »

Quality Assurance, Tablet Manufacturing

SOP for Tablet Dedusting Process

Posted on By

Standard Operating Procedure (SOP) for Tablet Dedusting Process Purpose The purpose of this SOP is to establish guidelines for the tablet dedusting process in pharmaceutical manufacturing. It ensures the removal of dust and excess particles from tablets, resulting in improved appearance, reduced contamination risks, and enhanced product quality. Scope This SOP applies to all personnel…

Read More “SOP for Tablet Dedusting Process” »

Tablet Manufacturing

SOP for Operation of Tablet Deduster

Posted on By

Standard Operating Procedure (SOP) for Operation of Tablet Deduster Purpose The purpose of this SOP is to provide guidelines for the safe and efficient operation of the tablet deduster in pharmaceutical manufacturing. It ensures the removal of dust and excess particles from tablets, maintaining product quality and compliance with regulatory standards. Scope This SOP applies…

Read More “SOP for Operation of Tablet Deduster” »

Tablet Manufacturing

Posts pagination

Previous 1 … 3 4 5 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:

 - 
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
  • Analytical Method Development V 2.0
  • API Manufacturing V 2.0
  • BA-BE Studies V 2.0
  • Biosimilars V 2.0
  • Capsules V 2.0
  • Creams V 2.0
  • Elixers 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