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SOP for Loading Film Rolls onto FFS Machine

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SOP for Loading Film Rolls onto FFS Machine

Standard Operating Procedure for Loading Film Rolls onto FFS Machine

1) Purpose

The purpose of this SOP is to define the procedure for safely and effectively loading film rolls onto the Form-Fill-Seal (FFS) machine to ensure smooth and efficient packaging operations.

2) Scope

This SOP applies to all personnel involved in the loading of film rolls onto FFS machines in the pharmaceutical manufacturing facility.

3) Responsibilities

3.1 Production Operators

  • Inspect film rolls for defects, damages, or discrepancies before loading.
  • Ensure proper alignment and loading of film rolls onto the FFS machine.
See also  SOP for Seal Integrity and Leak Testing

3.2 Quality Assurance (QA) Personnel

  • Verify the condition of film rolls and compliance with specifications.
  • Monitor loading process to prevent errors that could affect product quality.

4) Procedure

4.1 Pre-Loading Preparation

  1. Retrieve film rolls from designated storage area.
  2. Inspect each roll for damages, tears, or contamination.

4.2 Loading Process

  1. Align the film roll with the machine’s feed mechanism.
  2. Thread the film through the machine according to manufacturer’s instructions.
  3. Securely attach the film roll to the machine to prevent slippage or misalignment.

4.3 Verification

  1. Verify correct alignment and tension of the film roll.
  2. Confirm proper engagement of the film with machine components.
See also  Injectables: SOP for Process Validation

4.4 Post-Loading Checks

  1. Perform initial checks to ensure film roll is securely loaded and ready for operation.
  2. Document loading process details and any observations for traceability.

5)

Abbreviations, if any

FFS: Form-Fill-Seal

6) Documents, if any

  • Film Roll Inspection Checklist
  • Loading Logbook

7) Reference, if any

ISO 13485: Medical devices — Quality management systems — Requirements for regulatory purposes
FDA Guidance for Industry: Current Good Manufacturing Practice for Finished Pharmaceuticals

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
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  • Good Distribution Practice
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  • Maintenance Dept.
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  • 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
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