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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 Ensuring Proper Sealing in Blister Packs – V 2.0

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This SOP outlines the process for ensuring proper sealing of blister packs containing tablets. The goal is to maintain product integrity, prevent contamination, and extend the shelf life of the tablets by ensuring that the seals are tight, secure, and free from defects.

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Tablet Manufacturing V2.0

Tablets: SOP for Visual Inspection of Packed Tablets – V 2.0

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This SOP describes the procedure for visual inspection of packed tablets to ensure that they meet the required quality standards. The goal is to detect any defects such as cracks, broken tablets, incorrect labeling, or packaging issues before the products are released for distribution.

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Tablet Manufacturing V2.0

Tablets: SOP for Label Printing and Verification for Tablet Packaging – V 2.0

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This SOP provides a systematic approach for the label printing and verification process during tablet packaging. It ensures that all packaging labels are correctly printed with accurate information, and that the labels are properly verified before the final packaging of the product.

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Tablet Manufacturing V2.0

Tablets: SOP for Primary and Secondary Packing of Tablets – V 2.0

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This SOP outlines the procedure for the primary and secondary packaging of tablets. The goal is to ensure that all tablet products are packed according to quality standards, regulatory requirements, and safety protocols.

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Tablet Manufacturing V2.0

Tablets: SOP for Ensuring Batch Code Legibility on Packaging – V 2.0

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The purpose of this SOP is to establish a systematic procedure for ensuring that batch codes are legible and correctly printed on tablet packaging. This ensures traceability, compliance with regulatory requirements, and product safety.

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Tablet Manufacturing V2.0

Tablets: SOP for Handling and Storage of Packaging Materials – V 2.0

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The purpose of this SOP is to outline the procedures for handling and storing packaging materials in a manner that ensures the integrity, quality, and compliance of these materials with Good Manufacturing Practices (GMP) and regulatory requirements.

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Tablet Manufacturing V2.0

Tablets: SOP for Monitoring Printing Inks Used in Packaging – V 2.0

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The purpose of this SOP is to ensure that printing inks used in the packaging of tablet products are monitored for quality, compliance with regulatory standards, and consistency in application.

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Tablet Manufacturing V2.0

Tablets: SOP for Preventing Mix-Ups in Packaging Areas – V 2.0

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The purpose of this SOP is to outline the procedures and practices to prevent mix-ups during the packaging process. It ensures that products are correctly labeled, packaged, and stored in compliance with GMP and regulatory requirements, avoiding cross-contamination or mistakes in product identification.

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Tablet Manufacturing V2.0

Tablets: SOP for Weight Control During Strip Packing Process – V 2.0

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The purpose of this SOP is to ensure that the weight of tablets in the strip packing process is accurately controlled to meet the specified weight range. This helps maintain product quality and compliance with regulatory standards.

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Tablet Manufacturing V2.0

Tablets: SOP for Cartoning and Final Packaging of Tablets – V 2.0

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The purpose of this SOP is to ensure that the final packaging and cartoning of tablets is performed accurately and efficiently. This includes ensuring that the product is correctly packed, labeled, and ready for shipping in compliance with Good Manufacturing Practices (GMP) and regulatory standards.

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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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