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SOP Guide for Pharma

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Revised SOPs for Tablet Manufacturing V2.0

Tablets: SOP for Spray Coating Techniques for Film Coating – V 2.0

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This SOP defines the spray coating techniques used for film coating tablets, ensuring uniform application of the coating, optimal coating thickness, and consistent quality throughout production.

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Tablet Manufacturing V2.0

Tablets: SOP for Preventing Picking and Sticking in Coated Tablets – V 2.0

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This SOP outlines the preventive measures and techniques for minimizing picking and sticking during the coating of tablets, ensuring high-quality coating with no defects in the final product.

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Tablet Manufacturing V2.0

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

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This SOP defines the procedures for determining the end-point in the granulation process, ensuring that granules achieve the desired physical properties, such as size, moisture content, and flowability, before moving to the next stage of tablet manufacturing.

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Tablet Manufacturing V2.0

Tablets: SOP for Using Fluidized Bed Processor in Tablet Manufacturing – V 2.0

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This SOP outlines the procedures for using a fluidized bed processor (FBP) in tablet manufacturing. The FBP is used for processes such as granulation, coating, and drying, ensuring that tablet quality meets the required specifications for uniformity, strength, and appearance.

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Tablet Manufacturing V2.0

Tablets: SOP for Moisture Control During Granule Drying – V 2.0

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This SOP outlines the procedures for controlling moisture levels during the granule drying process, ensuring that the granules achieve the desired moisture content, which is critical for the consistency and quality of the final tablet product.

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Tablet Manufacturing V2.0

Tablets: SOP for Real-Time Monitoring of Tablet Coating Thickness – V 2.0

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This SOP outlines the procedures for real-time monitoring of tablet coating thickness during the coating process, ensuring that the applied coating is within specified limits for uniformity and quality.

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Tablet Manufacturing V2.0

Tablets: SOP for Compression Tooling Inspection and Cleaning – V 2.0

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This SOP outlines the procedure for the inspection and cleaning of compression tooling used in tablet manufacturing. Ensuring the proper condition of tooling is crucial to maintain tablet quality, prevent defects, and avoid cross-contamination.

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Tablet Manufacturing V2.0

Tablets: SOP for Granule Bulk Density Determination – V 2.0

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This SOP defines the procedure for determining the bulk density of granules, which is an important parameter for ensuring uniformity in tablet formulations. The bulk density of granules impacts the flowability, compressibility, and final tablet weight, all critical factors in tablet production.

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Tablet Manufacturing V2.0

Tablets: SOP for Anti-Dusting Measures in Tablet Compression – V 2.0

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This SOP defines the procedures for implementing anti-dusting measures during tablet compression to ensure a safe and clean environment. Reducing dust in the compression process is critical to improving tablet quality, protecting the operators, and maintaining compliance with Good Manufacturing Practices (GMP).

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Tablet Manufacturing V2.0

Tablets: SOP for Continuous Tablet Manufacturing Process – V 2.0

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This SOP outlines the procedures for the continuous tablet manufacturing process. The goal is to ensure efficient, consistent, and high-quality tablet production with minimal downtime and waste. Continuous manufacturing enables real-time monitoring and control of the production parameters.

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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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