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SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

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Tag: Documentation

SOP for Operation Of Disintegration Test Machine

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Standard Operating Procedure (SOP): Operation of Disintegration Test Machine Purpose: The purpose of this Standard Operating Procedure (SOP) is to provide detailed instructions for the proper operation of the Disintegration Test Machine. This SOP ensures accurate and reliable evaluation of the disintegration time of solid dosage forms. Scope: This SOP applies to all personnel involved…

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Quality Assurance

SOP for Operation of HPLC Machine

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Standard Operating Procedure (SOP): Operation of High-Performance Liquid Chromatography (HPLC) Purpose: The purpose of this Standard Operating Procedure (SOP) is to provide detailed instructions for the proper operation of the High-Performance Liquid Chromatography (HPLC) machine. This SOP ensures accurate and reliable analysis of samples using HPLC techniques. Scope: This SOP applies to all personnel involved…

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Quality Control

SOP for Operation of Friability Test Machine

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Standard Operating Procedure (SOP): Operation of Friability Test Machine Purpose: The purpose of this Standard Operating Procedure (SOP) is to provide detailed instructions for the proper operation of the Friability Test Machine. This SOP ensures accurate and reliable results during the evaluation of the physical integrity of tablets or pellets. Scope: This SOP applies to…

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Quality Control

SOP for Stability Study Report Preparation

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SOP for Stability Study Report Preparation: General steps that can be followed: 1. Identify the objective of the stability study and the regulatory guidelines that need to be adhered to. 2. Collect and record all relevant information for the study such as the product name, lot number, manufacturing date, expiration date, storage conditions, and analytical…

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Quality Control

SOP for Stability Study Protocol Preparation

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SOPs for stability study protocol preparation: 1. Identify the objective of the stability study clearly. This should include the purpose of the study, the samples being studied, the duration of the study, and the expected outcome. 2. Use established guidelines and regulations such as International Council for Harmonisation (ICH) guidelines and Good Manufacturing Practices (GMP)…

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Quality Control

Raw Material Sampling Plan: Procedure for Water Sampling

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The Raw Material Sampling Plan Procedure for Water outlined in this SOP is critical to ensuring the quality and safety of the water used in the manufacturing processes. By following this procedure, the company can ensure that all water used in the manufacturing processes meets the specified quality standards and does not pose any health…

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Raw Material Stores

SOP for The Raw Material Receipt Procedure outlined in this.

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The Raw Material Receipt Procedure outlined in this SOP is critical to ensuring the quality and integrity of the raw materials used in the company’s production processes. By following this procedure, the company can ensure that all raw materials received meet the quality standards set by the company and are stored appropriately to maintain their…

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Raw Material Stores

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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

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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.

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