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SOP for In-Process Checkweigher

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SOP for In-Process Checkweigher

Standard Operating Procedure for Using In-Process Checkweigher

1) Purpose

The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the in-process checkweigher in the pharmaceutical manufacturing of otic dosage forms to ensure accurate weight measurement during the manufacturing process.

2) Scope

This SOP applies to all personnel involved in the operation and maintenance of in-process checkweighers in the pharmaceutical manufacturing facility.

3) Responsibilities

Operators: Responsible for correctly operating the in-process checkweigher as per this SOP.
Quality Control (QC) Personnel: Responsible for monitoring and verifying the accuracy of weight measurements.
Maintenance Personnel: Responsible for maintaining the in-process checkweigher in proper working condition.

See also  SOP for PCR Machine

4) Procedure

4.1 Pre-operation Checks
4.1.1 Inspection
4.1.1.1 Inspect the in-process checkweigher for cleanliness and integrity before use.
4.1.1.2 Ensure that the checkweigher is properly calibrated and functioning.
4.1.1.3 Check that the weighing platform and conveyor belt are free from any obstructions.

4.1.2 Preparation
4.1.2.1 Ensure that the materials to be weighed are suitable for the checkweigher.
4.1.2.2 Set up the checkweigher according to the specific requirements of the product batch.

4.1.2.3 Enter the required weight parameters and tolerance limits into the checkweigher’s control panel.

4.2 Operation
4.2.1 Weighing Process
4.2.1.1 Power on the in-process checkweigher and start the conveyor belt.
4.2.1.2 Feed the product items onto the conveyor belt for weighing.
4.2.1.3 Monitor the display to ensure that all items are being weighed accurately within the set tolerance limits.

See also  SOP for Compounder

4.2.2 Safety Precautions
4.2.2.1 Wear appropriate PPE when operating the checkweigher.
4.2.2.2 Handle products carefully to prevent damage or contamination.
4.2.2.3 Follow all safety protocols for working with moving machinery.

4.3 Post-operation
4.3.1 Shutdown
4.3.1.1 Stop the conveyor belt and power off the checkweigher after completing the weighing process.
4.3.1.2 Remove any remaining products from the weighing platform.
4.3.1.3 Clean the weighing platform and conveyor belt with appropriate cleaning agents.

4.3.2 Maintenance
4.3.2.1 Regularly inspect the checkweigher for wear and tear, and perform necessary repairs.
4.3.2.2 Calibrate the checkweigher periodically to ensure accurate measurements.
4.3.2.3 Keep maintenance records and document any issues or repairs performed.

See also  SOP for Nitrogen Evaporator

5) Abbreviations, if any

QC: Quality Control
SOP: Standard Operating Procedure
PPE: Personal Protective Equipment

6) Documents, if any

Weighing log
Maintenance records for the in-process checkweigher

7) Reference, if any

Manufacturer’s manual for the in-process checkweigher
Pharmacopeial guidelines for in-process weight control in pharmaceutical manufacturing

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

  • 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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