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SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

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Tag: documentation in powder manufacturing

SOP for Particle Morphology Testing in Powders

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SOP for Particle Morphology Testing in Powders Standard Operating Procedure for Particle Morphology Testing in Powders 1) Purpose The purpose of this SOP is to provide guidelines for the testing of particle morphology in powders within the pharmaceutical industry. Particle morphology testing assesses the shape, size, and surface characteristics of powder particles, which are critical…

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Powder & Granules

SOP for Granule Hardness Testing

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SOP for Granule Hardness Testing Standard Operating Procedure for Granule Hardness Testing 1) Purpose The purpose of this SOP is to provide guidelines for the testing of granule hardness during the manufacturing process of granules within the pharmaceutical industry. Granule hardness testing ensures that granules have sufficient mechanical strength to withstand subsequent processing steps without…

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Powder & Granules

SOP for Use of Glidants in Powders Production

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SOP for Use of Glidants in Powders Production Standard Operating Procedure for Use of Glidants in Powders Production 1) Purpose The purpose of this SOP is to provide guidelines for the proper use of glidants in the manufacturing of powders within the pharmaceutical industry. Glidants are additives that improve the flow properties of powders by…

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Powder & Granules

SOP for Use of Surfactants in Powders Production

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SOP for Use of Surfactants in Powders Production Standard Operating Procedure for Use of Surfactants in Powders Production 1) Purpose The purpose of this SOP is to provide guidelines for the proper use of surfactants in the manufacturing of powders within the pharmaceutical industry. Surfactants are used to improve wetting, dispersion, and solubility of active…

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Powder & Granules

SOP for Use of Disintegrants in Powders Production

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SOP for Use of Disintegrants in Powders Production Standard Operating Procedure for Use of Disintegrants in Powders Production 1) Purpose The purpose of this SOP is to provide guidelines for the proper use of disintegrants in the manufacturing of powders within the pharmaceutical industry. Disintegrants are essential additives that promote the rapid breakup of tablets…

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Powder & Granules

SOP for Use of Lubricants in Powders Production

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SOP for Use of Lubricants in Powders Production Standard Operating Procedure for Use of Lubricants in Powders Production 1) Purpose The purpose of this SOP is to provide guidelines for the proper use of lubricants in the manufacturing of powders within the pharmaceutical industry. Lubricants are essential for improving powder flow properties, preventing adhesion, and…

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Powder & Granules

SOP for Use of Binders in Granules Production

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SOP for Use of Binders in Granules Production Standard Operating Procedure for Use of Binders in Granules Production 1) Purpose The purpose of this SOP is to provide guidelines for the proper use of binders in the granulation process during pharmaceutical manufacturing. Binders are crucial for ensuring cohesive granules that can be further processed into…

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Powder & Granules

SOP for Dry Granulation

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SOP for Dry Granulation Standard Operating Procedure for Dry Granulation 1) Purpose The purpose of this SOP is to provide guidelines for the dry granulation process in pharmaceutical manufacturing, ensuring efficient and reproducible granule formation from powders that are sensitive to moisture or heat. 2) Scope This SOP applies to all personnel involved in the…

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Powder & Granules

SOP for Freeze Drying in Powders Production

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SOP for Freeze Drying in Powders Production Standard Operating Procedure for Freeze Drying in Powders Production 1) Purpose The purpose of this SOP is to provide guidelines for the freeze drying (lyophilization) process in pharmaceutical manufacturing, specifically for converting liquid formulations into dry powders under low temperature and pressure conditions. 2) Scope This SOP applies…

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Powder & Granules

Powder & Granules: SOP for Dry Granulation

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SOP for Dry Granulation Standard Operating Procedure for Dry Granulation 1) Purpose The purpose of this SOP is to provide guidelines for the dry granulation process in pharmaceutical manufacturing, ensuring efficient and reproducible granule formation from powders that are sensitive to moisture or heat. 2) Scope This SOP applies to all personnel involved in the…

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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
  • API Manufacturing V 2.0
  • BA-BE Studies V 2.0
  • Capsules V 2.0
  • Creams 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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