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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 Preventing Contamination in Powders Production

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The purpose of this SOP is to establish procedures to prevent contamination during powders production in the pharmaceutical industry, ensuring product quality and safety.
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Powder & Granules

SOP for Maintaining Sterility in Granules Production

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The purpose of this SOP is to establish procedures for maintaining sterility throughout the granules production process in the pharmaceutical industry to prevent contamination and ensure product quality.
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Powder & Granules

SOP for Maintaining Sterility in Powders Production

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The purpose of this SOP is to establish procedures for maintaining sterility throughout the powders production process in the pharmaceutical industry to prevent contamination and ensure product quality.
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Powder & Granules

SOP for Raw Material Inspection for Granules

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The purpose of this SOP is to define the procedures for the inspection and testing of raw materials used in granules production within the pharmaceutical industry to ensure quality, safety, and compliance with specifications.
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Powder & Granules

SOP for Raw Material Inspection for Powders

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The purpose of this SOP is to define the procedures for the inspection and testing of raw materials used in powders production within the pharmaceutical industry to ensure quality, safety, and compliance with specifications.
Click to read the full article.

Powder & Granules

SOP for Training Personnel in Granules Production

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The purpose of this SOP is to establish procedures for the training of personnel involved in granules production within the pharmaceutical industry to ensure competency, adherence to procedures, and compliance with regulatory requirements.
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Powder & Granules

SOP for Training Personnel in Powders Production

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The purpose of this SOP is to establish procedures for the training of personnel involved in powders production within the pharmaceutical industry to ensure competency, adherence to procedures, and compliance with regulatory requirements.
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Powder & Granules

SOP for Documentation in Granules Production

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The purpose of this SOP is to outline the procedures for documenting various activities and processes involved in granules production in the pharmaceutical industry to ensure traceability, accountability, and regulatory compliance.
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Powder & Granules

SOP for Documentation in Powders Production

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The purpose of this SOP is to outline the procedures for documenting various activities and processes involved in powders production in the pharmaceutical industry to ensure traceability, accountability, and regulatory compliance.
Click to read the full article.

Powder & Granules

SOP for Handling and Disposal of Waste in Granules Production

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The purpose of this SOP is to establish guidelines for the proper handling, segregation, and disposal of waste generated during granules production in the pharmaceutical industry to ensure environmental safety and regulatory compliance.
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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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