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SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

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Tag: Tablet coating procedure

SOP for Handling and Maintenance of Disintegration Testing Equipment

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Standard Operating Procedure for Handling and Maintenance of Disintegration Testing Equipment Purpose The purpose of this SOP is to provide comprehensive guidelines for the proper handling and maintenance of disintegration testing equipment in pharmaceutical manufacturing. Proper handling and regular maintenance of the equipment are essential to ensure accurate and reliable disintegration test results, contributing to…

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Quality Control, Tablet Manufacturing

SOP for Calibration and Verification of Disintegration Tester:

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Standard Operating Procedure for Calibration & Verification of Disintegration Tester Purpose The purpose of this SOP is to establish comprehensive guidelines for the calibration and verification of the disintegration tester in pharmaceutical manufacturing. Calibration and verification ensure the accuracy and reliability of disintegration test results, leading to confident decisions on product quality and adherence to…

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Quality Control, Tablet Manufacturing

Quality Control, Tablet Manufacturing: SOP for Tablet Disintegration Testing:

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Standard Operating Procedure for Tablet Disintegration Test Purpose The purpose of this SOP is to provide detailed guidelines for conducting tablet disintegration testing in pharmaceutical manufacturing. Disintegration testing is a critical quality control parameter that assesses the time it takes for tablets to disintegrate into smaller particles in simulated gastrointestinal fluids. This SOP aims to…

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Quality Control, Tablet Manufacturing

SOP for Operation of Tablet Disintegration Tester

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Standard Operating Procedure for Operation of Tablet Disintegration Tester Purpose The purpose of this SOP is to provide detailed guidelines for the proper operation of the tablet disintegration tester in pharmaceutical manufacturing. Disintegration testing is a critical quality control test that evaluates the time it takes for tablets to disintegrate into smaller particles in simulated…

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Quality Control, Tablet Manufacturing

SOP for Handling and Maintenance of Friability Testing Equipment

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Standard Operating Procedure for Handling and Maintenance of Friability Testing Equipment Purpose The purpose of this SOP is to provide comprehensive guidelines for the proper handling and maintenance of friability testing equipment in pharmaceutical manufacturing. Proper handling and regular maintenance of the equipment are essential to ensure accurate and reliable friability test results, contributing to…

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Quality Control, Tablet Manufacturing

SOP for Calibration and Verification of Friability Tester

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Standard Operating Procedure for Calibration and Verification of Friability Tester Purpose The purpose of this SOP is to establish comprehensive guidelines for the calibration and verification of the friability tester in pharmaceutical manufacturing. Calibration and verification ensure the accuracy and reliability of friability test results, leading to confident decisions on product quality and adherence to…

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Quality Control, Tablet Manufacturing

Quality Control, Tablet Manufacturing: SOP for Tablet Friability Testing

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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…

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Quality Control, Tablet Manufacturing

SOP for Operation of Tablet Friability Tester

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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…

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Tablet Manufacturing

SOP for Handling and Maintenance of Hardness Testing Equipment

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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…

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Tablet Manufacturing

SOP for Calibration and Verification of Hardness Tester

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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…

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Tablet Manufacturing

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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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