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: Quality management systems SOP

SOP for Regulatory Laboratory Controls and Testing

Posted on By

Standard Operating Procedure (SOP) for Regulatory Laboratory Controls and Testing Purpose: The purpose of this SOP is to establish the procedures for regulatory laboratory controls and testing to ensure compliance with applicable regulations and standards. It defines the processes for laboratory testing, documentation, equipment calibration and maintenance, sample handling, and reporting of test results. Effective…

Read More “SOP for Regulatory Laboratory Controls and Testing” »

Quality Assurance

SOP for Regulatory Supplier Qualification and Management

Posted on By

Standard Operating Procedure (SOP) for Regulatory Supplier Qualification and Management Purpose: The purpose of this SOP is to outline the process and requirements for the qualification and management of suppliers in regulatory affairs. It ensures that suppliers meet the necessary criteria for providing goods or services that are critical to regulatory activities. Effective supplier qualification…

Read More “SOP for Regulatory Supplier Qualification and Management” »

Regulatory Affairs

SOP for Regulatory Data Integrity

Posted on By

Standard Operating Procedure (SOP) for Regulatory Data Integrity Purpose: The purpose of this SOP is to establish guidelines and procedures to ensure data integrity in regulatory activities. It aims to prevent unauthorized access, loss, alteration, or falsification of data throughout the regulatory processes, including data generation, collection, analysis, and reporting. Adherence to data integrity principles…

Read More “SOP for Regulatory Data Integrity” »

Regulatory Affairs

SOP for Regulatory Good Distribution Practices (GDP)

Posted on By

Standard Operating Procedure (SOP) for Regulatory Good Distribution Practices (GDP) Purpose: The purpose of this SOP is to establish guidelines and procedures for ensuring compliance with Good Distribution Practices (GDP) for pharmaceutical products. The SOP aims to maintain the integrity, quality, and safety of distributed products throughout the supply chain, from storage to transportation and…

Read More “SOP for Regulatory Good Distribution Practices (GDP)” »

Regulatory Affairs

SOP for Regulatory Annual Product Quality Review

Posted on By

Standard Operating Procedure (SOP) for Regulatory Annual Product Quality Review Purpose: The purpose of this SOP is to establish a systematic process for conducting annual product quality reviews (APQRs) to assess the overall quality performance of regulated products. The APQRs provide a comprehensive evaluation of product quality and ensure ongoing compliance with regulatory requirements. Scope:…

Read More “SOP for Regulatory Annual Product Quality Review” »

Quality Assurance

SOP for Regulatory Advertising and Promotional Material Review

Posted on By

Standard Operating Procedure (SOP) for Regulatory Advertising and Promotional Material Review Purpose: The purpose of this SOP is to establish a systematic and compliant process for the review and approval of advertising and promotional materials related to regulated products. The SOP ensures adherence to applicable regulatory requirements, protects the integrity of product claims, and maintains…

Read More “SOP for Regulatory Advertising and Promotional Material Review” »

Regulatory Affairs

SOP for Regulatory Electronic Document Management Systems

Posted on By

Standard Operating Procedure (SOP) for Regulatory Electronic Document Management Systems Purpose: The purpose of this SOP is to establish guidelines for the efficient and effective management of regulatory electronic documents within the organization. The SOP aims to ensure compliance with regulatory requirements, facilitate document control and versioning, and promote accessibility and traceability of electronic documents…

Read More “SOP for Regulatory Electronic Document Management Systems” »

Regulatory Affairs

SOP for Regulatory Patent and Intellectual Property Management

Posted on By

Standard Operating Procedure (SOP) for Regulatory Patent and Intellectual Property Management Purpose: The purpose of this SOP is to establish a standardized process for managing regulatory patents and intellectual property (IP) within the organization. The SOP aims to ensure compliance with IP laws and regulations, protect the organization’s inventions and innovations, and facilitate effective IP…

Read More “SOP for Regulatory Patent and Intellectual Property Management” »

Regulatory Affairs

SOP for Regulatory Due Diligence

Posted on By

Standard Operating Procedure (SOP) for Regulatory Due Diligence Purpose: The purpose of this SOP is to establish a standardized process for conducting regulatory due diligence in the context of business transactions, such as mergers, acquisitions, partnerships, or licensing agreements. The regulatory due diligence aims to identify and assess potential regulatory risks, compliance issues, and any…

Read More “SOP for Regulatory Due Diligence” »

Regulatory Affairs

SOP for Regulatory Track and Trace Systems

Posted on By

Standard Operating Procedure (SOP) for Regulatory Track and Trace Systems Purpose: The purpose of this SOP is to establish a standardized process for the implementation, maintenance, and management of regulatory track and trace systems. The track and trace systems aim to ensure the secure and accurate tracing of pharmaceutical products throughout the supply chain, enabling…

Read More “SOP for Regulatory Track and Trace Systems” »

Regulatory Affairs

Posts pagination

1 2 … 4 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