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:

SOP for Batch Sampling and Testing

Posted on By

Standard Operating Procedure for Batch Sampling and Testing 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the systematic and controlled sampling and testing of batches in the pharmaceutical manufacturing process. This SOP ensures that representative samples are collected and tested for quality attributes, ensuring that the batch meets…

Read More “SOP for Batch Sampling and Testing” »

Quality Control, Tablet Manufacturing

Tablet Manufacturing: SOP for Batch Record Review and Approval

Posted on By

Standard Operating Procedure for Batch Record Review and Approval 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the systematic and thorough review and approval of batch records in the pharmaceutical manufacturing facility. This SOP ensures that each batch record is meticulously examined for accuracy, completeness, and compliance with…

Read More “Tablet Manufacturing: SOP for Batch Record Review and Approval” »

Tablet Manufacturing

SOP for Batch Release and Product Release

Posted on By

Standard Operating Procedure for Batch Release and Product Release 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the systematic and controlled process of batch release and product release in the pharmaceutical manufacturing facility. This SOP ensures that each batch of pharmaceutical products undergoes thorough review, testing, and verification…

Read More “SOP for Batch Release and Product Release” »

Tablet Manufacturing

SOP for Batch Record Preparation and Documentation

Posted on By

Standard Operating Procedure for Batch Record Preparation and Documentation 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the proper preparation and documentation of batch records in the pharmaceutical manufacturing process. This SOP ensures that batch records are accurately and comprehensively documented, reflecting all critical steps, measurements, and observations…

Read More “SOP for Batch Record Preparation and Documentation” »

Tablet Manufacturing

SOP for Equipment Verification and Calibration

Posted on By

Standard Operating Procedure for Equipment Verification and Calibration 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the verification and calibration of equipment used in the pharmaceutical manufacturing process. This SOP ensures that all equipment is regularly checked for accuracy, precision, and compliance with required specifications to maintain the…

Read More “SOP for Equipment Verification and Calibration” »

Quality Assurance, Tablet Manufacturing

SOP for Handling and Transporting Tablets within the Manufacturing Department

Posted on By

Standard Operating Procedure for Handling and Transporting Tablets within the Department 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to establish guidelines for the safe and proper handling and transportation of tablets within the manufacturing department. This SOP aims to minimize the risk of tablet damage, contamination, and mix-up during handling and…

Read More “SOP for Handling and Transporting Tablets within the Manufacturing Department” »

Tablet Manufacturing

SOP for Inventory Control and Stock Rotation

Posted on By

Standard Operating Procedure for Inventory Control and Stock Rotation 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to establish guidelines for the effective inventory control and stock rotation of pharmaceutical products within the manufacturing facility. This SOP aims to ensure that the oldest stock is used first (first-in-first-out, FIFO), minimize product expiry,…

Read More “SOP for Inventory Control and Stock Rotation” »

Tablet Manufacturing

SOP for Tablet Storage and Retrieval

Posted on By

Standard Operating Procedure for Tablet Storage and Retrieval 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the proper storage, organization, and retrieval of tablets in the pharmaceutical manufacturing facility. This SOP ensures that tablets are stored under controlled conditions, easily accessible, and that the correct inventory is maintained…

Read More “SOP for Tablet Storage and Retrieval” »

Tablet Manufacturing

SOP for operation of Tablet Storage and Handling Equipment

Posted on By

Standard Operating Procedure for Operation of Tablet Storage and Handling Equipment 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the proper operation and handling of tablet storage equipment to ensure the storage conditions meet the required specifications, prevent contamination, and maintain the quality of the tablets during storage….

Read More “SOP for operation of Tablet Storage and Handling Equipment” »

Tablet Manufacturing

SOP for Handling and Rejection of Defective Tablets

Posted on By

Standard Operating Procedure for Handling and Rejection of Defective Tablets 1. Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the proper handling and rejection of defective tablets identified during the manufacturing or inspection process. This SOP ensures that defective tablets are segregated, properly disposed of, and that appropriate actions…

Read More “SOP for Handling and Rejection of Defective Tablets” »

Tablet Manufacturing

Posts pagination

1 2 … 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