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SOP for Tablet Sorting Machine

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SOP for Tablet Sorting Machine

Operation and Maintenance of Tablet Sorting Machine

1) Purpose

The purpose of this SOP is to outline the procedures for operating and maintaining the tablet sorting machine to ensure accurate sorting and inspection of tablets.

2) Scope

This SOP applies to all personnel involved in the operation, cleaning, and maintenance of the tablet sorting machine in the manufacturing facility.

3) Responsibilities

It is the responsibility of production operators, maintenance staff, and quality control personnel to follow this SOP to ensure proper operation and maintenance of the tablet sorting machine.

4) Procedure

4.1 Preparation

  1. Ensure the work area and equipment are clean and sanitized before starting the sorting process.
  2. Verify the availability and integrity of tablets ready for sorting.
  3. Inspect the tablet sorting machine, including sorting trays and detection sensors, to ensure they are clean and properly calibrated.
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4.2 Sorting Process

  1. Set up the sorting parameters such as size, shape, color, and defects according to product specifications.
  2. Load the tablets into the sorting trays and start the sorting process.
  3. Monitor the sorting process to ensure accurate separation and rejection of defective tablets.

4.3 Cleaning and Maintenance

  1. Stop the tablet sorting machine after completing the sorting batch.
  2. Clean the sorting trays, detection sensors, and conveyor belts thoroughly to remove any tablet residues.
  3. Perform routine maintenance tasks such
as calibration of detection sensors and lubrication of sorting mechanisms.

5) Abbreviations, if any

N/A

6) Documents, if any

Batch production record, Cleaning log, Tablet sorting specifications

7) Reference, if any

GMP guidelines, Manufacturer’s operating manual for tablet sorting machine

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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