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SOP for Crimping Machine

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SOP for Crimping Machine

Standard Operating Procedure for Using Crimping Machine

1) Purpose

The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the crimping machine used in the manufacturing of otic dosage forms to ensure secure and consistent crimping of containers.

2) Scope

This SOP applies to all personnel involved in the operation and maintenance of the crimping machine in the pharmaceutical manufacturing facility.

3) Responsibilities

Operators: Responsible for correctly operating the crimping machine as per this SOP.
Quality Control (QC) Personnel: Responsible for monitoring the crimping process and verifying the integrity of the crimps.
Maintenance Personnel: Responsible for maintaining the crimping machine in proper working condition.

See also  SOP for pH Meter

4) Procedure

4.1 Operation
4.1.1 Preparation
4.1.1.1 Ensure the crimping machine is on a stable, level surface.
4.1.1.2 Check that the machine is clean and free of any debris.
4.1.1.3 Verify that the machine is properly calibrated and functioning.

4.1.2 Loading the Machine
4.1.2.1 Prepare the containers to be crimped as per the batch record.
4.1.2.2 Open the machine’s loading port and place the containers inside.
4.1.2.3

Close and secure the loading port.

4.1.3 Crimping Process
4.1.3.1 Select the appropriate crimping parameters (e.g., pressure, time) as per the batch record.
4.1.3.2 Start the machine and monitor the crimping process.
4.1.3.3 Ensure that each container is crimped securely and consistently.
4.1.3.4 After the crimping cycle is complete, stop the machine.

See also  SOP for Emulsion Preparation Unit

4.1.4 Unloading the Machine
4.1.4.1 Carefully remove the crimped containers from the machine.
4.1.4.2 Inspect the containers to ensure they are properly crimped and free from defects.

4.2 Calibration
4.2.1 Daily Check
4.2.1.1 Perform a daily check of the machine’s settings and indicators.
4.2.1.2 Record the results in the equipment log.

4.2.2 Monthly Calibration
4.2.2.1 Conduct a full calibration of the crimping machine monthly using standard test methods.
4.2.2.2 Document the calibration results and any adjustments made.

4.3 Maintenance
4.3.1 Routine Maintenance
4.3.1.1 Clean the machine and all parts regularly to prevent contamination.
4.3.1.2 Inspect the machine for any signs of wear or damage and replace parts as necessary.

See also  SOP for Volumetric Filling Machine

4.3.2 Troubleshooting
4.3.2.1 If the machine displays error messages or fails to reach the required conditions, refer to the manufacturer’s manual for troubleshooting steps.
4.3.2.2 Contact maintenance personnel if the issue cannot be resolved.

5) Abbreviations, if any

QC: Quality Control
SOP: Standard Operating Procedure

6) Documents, if any

Crimping log
Maintenance log

7) Reference, if any

Manufacturer’s manual for the crimping machine
Regulatory guidelines for equipment calibration and maintenance

8) SOP Version

Version 1.0

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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

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