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SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

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SOPs for Powder & Granules

SOP for Stability Testing of Powders

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The purpose of this SOP is to provide a standardized procedure for conducting stability testing of powders in the pharmaceutical manufacturing process to assess their shelf-life under various storage conditions.
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Powder & Granules

SOP for Packaging of Granules

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The purpose of this SOP is to provide a standardized procedure for the packaging of granules in the pharmaceutical manufacturing process to ensure product integrity, quality, and compliance with regulatory requirements.
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Powder & Granules

SOP for Packaging of Powders

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The purpose of this SOP is to provide a standardized procedure for the packaging of powders in the pharmaceutical manufacturing process to ensure product integrity, quality, and compliance with regulatory requirements.
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Powder & Granules

SOP for Quality Control Testing of Granules

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The purpose of this SOP is to provide a standardized procedure for the quality control testing of granules in the pharmaceutical manufacturing process to ensure they meet the required specifications for safety, efficacy, and quality.
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Powder & Granules

SOP for Quality Control Testing of Powders

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The purpose of this SOP is to provide a standardized procedure for the quality control testing of powders in the pharmaceutical manufacturing process to ensure they meet the required specifications for safety, efficacy, and quality.
Click to read the full article.

Powder & Granules

SOP for Granulation Techniques

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The purpose of this SOP is to provide a standardized procedure for the different granulation techniques used in pharmaceutical manufacturing to ensure consistency, quality, and compliance with regulatory requirements.
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Powder & Granules

SOP for Blending of Powders

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The purpose of this SOP is to provide a standardized procedure for the blending of powders in the pharmaceutical manufacturing process to ensure uniformity, quality, and compliance with regulatory requirements.
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Powder & Granules

SOP for Preparation of Granules

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The purpose of this SOP is to provide a standardized procedure for the preparation of granules in the pharmaceutical manufacturing process to ensure consistency, quality, and compliance with regulatory requirements.
Click to read the full article.

Powder & Granules

SOP for Preparation of Powders

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The purpose of this SOP is to provide a standardized procedure for the preparation of powders in the pharmaceutical manufacturing process to ensure consistency, quality, and compliance with regulatory requirements.
Click to read the full article.

Powder & Granules

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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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