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SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

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Revised SOPs for Tablet Manufacturing V2.0

Tablets: SOP for End-Point Determination in Wet Granulation – V 2.0

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To define the procedure for determining the end-point in the wet granulation process to ensure that the granules achieve the desired properties such as adequate size, uniformity, and moisture content before moving to the next stage of tablet manufacturing.

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Tablet Manufacturing V2.0

Tablets: SOP for Lubrication Testing in Tablet Granules – V 2.0

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To define the procedure for testing the lubrication properties of tablet granules to ensure proper flowability, ease of compression, and tablet release during manufacturing.

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Tablet Manufacturing V2.0

Tablets: SOP for Dissolution Testing for First Batch Release of Tablets – V 2.0

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To define the procedure for performing dissolution testing on the first batch of tablets before release to ensure that the tablets meet the required dissolution profile for proper drug release and bioavailability.

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Tablet Manufacturing V2.0

Tablets: SOP for Weight Uniformity During Coating Process – V 2.0

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To define the procedure for ensuring weight uniformity during the coating process of tablets, ensuring that the weight of each tablet is consistent and meets the required specifications for product quality.

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Tablet Manufacturing V2.0

Tablets: SOP for Cleaning Verification of Coating Pans Between Batches – V 2.0

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To define the procedure for cleaning and verifying the cleanliness of coating pans between batches to prevent cross-contamination and ensure product quality.

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Tablet Manufacturing V2.0

Tablets: SOP for Monitoring Spray Rate in Coating Machines – V 2.0

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To define the procedure for monitoring the spray rate in coating machines during tablet coating, ensuring uniform and controlled application of the coating material to the tablets.

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Tablet Manufacturing V2.0

Tablets: SOP for Tablet Temperature Control During Compression – V 2.0

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To define the procedure for controlling and monitoring tablet temperature during the compression process to ensure proper tablet formation and avoid damage to the active ingredients or excipients.

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Tablet Manufacturing V2.0

Tablets: SOP for Real-Time Data Logging in In-Process Monitoring – V 2.0

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To define the procedure for real-time data logging during in-process monitoring of tablet manufacturing to ensure accurate recording, traceability, and compliance with production specifications.

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Tablet Manufacturing V2.0

Tablets: SOP for Core Tablet Inspection Before Film Coating – V 2.0

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To define the procedure for inspecting core tablets before the application of the film coating, ensuring that the core tablets meet the required quality specifications for coating application.

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Tablet Manufacturing V2.0

Tablets: SOP for pH Monitoring in Coating Suspensions – V 2.0

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To define the procedure for monitoring the pH of coating suspensions used in tablet film coating processes to ensure that the pH remains within the acceptable range for optimal coating quality and stability.

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Tablet Manufacturing V2.0

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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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