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SOP for Labeling and Coding on FFS Machine

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SOP for Labeling and Coding on FFS Machine

Standard Operating Procedure for Labeling and Coding on FFS Machine

1) Purpose

The purpose of this SOP is to outline the procedures for labeling and coding pharmaceutical products on the Form-Fill-Seal (FFS) machine to ensure accurate product identification and compliance with regulatory requirements.

2) Scope

This SOP applies to the labeling and coding activities conducted on FFS machines during pharmaceutical manufacturing processes.

3) Responsibilities

3.1 Production Operators

  • Ensure correct setup and operation of labeling and coding systems.
  • Monitor label and code application for accuracy and legibility.

3.2 Quality Control (QC) Personnel

  • Verify labeling and coding accuracy and compliance with specifications.
  • Perform inspections and checks to prevent labeling errors.
See also  SOP for Recall Procedures

4) Procedure

4.1 Setup and Calibration

  1. Calibrate labeling and coding equipment according to manufacturer’s instructions.
  2. Verify correct placement and alignment of labels and codes.

4.2 Labeling Process

  1. Load labeling materials onto the FFS machine in designated feeders.
  2. Initiate label application process and monitor for proper adherence.

4.3 Coding Process

  1. Input product-specific codes into the coding system.
  2. Activate coding mechanism and ensure accurate printing or embossing.

4.4 Inspection and Verification

  1. Inspect labeled and coded products for accuracy and clarity.
  2. Reject any products with labeling or coding defects and document findings.

5) Abbreviations, if any

FFS: Form-Fill-Seal
QC: Quality Control

6) Documents, if any

  • Labeling and Coding Setup Checklist
  • Inspection and Verification Logs
See also  SOP for Handling and Disposal of Waste Materials from FFS Machine

7) Reference, if any

ISO

15378: Primary packaging materials for medicinal products — Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP)
FDA Guidance for Industry: Labeling OTC Human Drug Products

8) SOP Version

Version 1.0

Injectables Tags:Analytical method validation for injections, Aseptic media fill trials SOP, Bioburden testing for injections, Cleaning validation for injection equipment, Emulsion stability testing for injections, Formulation development for injections, Homogeneity testing for injections, IM injection SOP, Injection filling volume accuracy, Injection stability testing, Intramuscular injection procedure, Intravenous injection guidelines, IV injection SOP, Needle assembly for syringes SOP, Packaging integrity testing for injections, Particle size analysis for injections, Pre-filled syringe stability testing, Product sterility in aseptic processing, Reconstitution testing for injections, SC injection SOP, Subcutaneous injection technique, Syringe filling and capping SOP, Syringe labeling and inspection SOP, Temperature mapping in storage areas, Viscosity testing for injections

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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

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