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SOP for Suppository Cooling Rack

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SOP for Suppository Cooling Rack

Operation and Maintenance of Suppository Cooling Rack

1) Purpose

The purpose of this SOP is to outline the procedures for operating and maintaining the suppository cooling rack to ensure effective cooling and solidification of suppositories during the manufacturing process.

2) Scope

This SOP applies to all personnel involved in the operation, cleaning, and maintenance of the suppository cooling rack 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 suppository cooling rack.

See also  SOP for Ring Coating Machine

4) Procedure

4.1 Preparation

  1. Ensure the work area and equipment are clean and sanitized before placing suppositories on the cooling rack.
  2. Verify the availability and integrity of suppositories ready for cooling.
  3. Inspect the suppository cooling rack, including trays and racks, to ensure they are clean and in good working condition.

4.2 Cooling Process

  1. Place suppositories on the designated trays of the cooling rack immediately after they are molded.
  2. Position the cooling rack in a designated cooling area with controlled temperature and humidity.
  3. Allow suppositories to cool and solidify as per the specified time in the manufacturing instructions.

4.3 Cleaning and Maintenance

  1. After suppositories are removed, clean the cooling rack thoroughly using approved cleaning agents.
  2. Inspect the cooling rack regularly for any signs of wear or damage, and repair or replace parts as necessary.
See also  SOP for Tablet Compression Machine

5) Abbreviations, if any

N/A

6) Documents, if any

Batch production record, Cleaning log, Suppository cooling rack specifications

7) Reference, if any

GMP guidelines, Manufacturer’s operating manual for suppository cooling rack

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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