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SOP for Calibration of Equipment Used for Powders

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SOP for Calibration of Equipment Used for Powders

Standard Operating Procedure for Calibration of Equipment Used for Powders

1) Purpose

The purpose of this SOP is to provide a standardized procedure for the calibration of equipment used in the manufacturing of powders in the pharmaceutical industry to ensure accurate and reliable performance.

2) Scope

This SOP applies to all personnel involved in the calibration of equipment used for powders within the pharmaceutical manufacturing facility.

3) Responsibilities

Quality Control Analysts: Responsible for performing calibration activities as per the SOP.
Engineering Department: Responsible for maintaining calibration schedules and records.
Quality Assurance: Responsible for reviewing calibration results and ensuring compliance.

See also  Powder & Granules: SOP for Dry Granulation

4) Procedure

  1. Identification of Equipment:
    1. Identify all equipment used for powders that require calibration.
    2. Document equipment details including identification number and calibration frequency.
  2. Calibration Schedule:
    1. Establish a calibration schedule based on manufacturer recommendations and regulatory requirements.
    2. Ensure calibration intervals are documented and adhered to.
  3. Preparation for Calibration:
    1. Notify relevant personnel about upcoming calibration activities.
    2. Prepare calibration standards and equipment as per calibration procedures.
  4. Calibration Process:
    1. Perform calibration procedures following documented instructions and using calibrated standards.
    2. Record calibration results accurately including deviations and adjustments made.
  5. Verification:
    1. Verify the calibrated equipment against acceptance criteria and specifications.
    2. Ensure the equipment meets performance standards before returning to service.
  6. Documentation:
    1. Complete calibration records including equipment details, calibration procedures used, and personnel involved.
    2. Ensure all documentation is reviewed, approved, and stored as per document control procedures.
See also  SOP for Compressibility Index Testing in Granules

5) Abbreviations, if any

SOP: Standard Operating Procedure
GMP: Good Manufacturing Practice

6) Documents, if any

Calibration SOP, Equipment Calibration Records

7) Reference, if any

International Conference on Harmonisation (ICH) guidelines and equipment manufacturer’s specifications.

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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