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Injectables: SOP for Quality Control Testing of IV Injections

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SOP for Quality Control Testing of IV Injections

Standard Operating Procedure for Quality Control Testing of IV Injections

1) Purpose

The purpose of this SOP is to define the procedures for conducting quality control testing of intravenous (IV) injections to ensure compliance with specifications and regulatory requirements.

2) Scope

This SOP applies to all quality control personnel responsible for testing IV injections in the pharmaceutical manufacturing facility.

3) Responsibilities

3.1 Quality Control (QC) Analysts

  • Perform testing and analysis of IV injections according to approved testing protocols.
  • Record and report testing results accurately and promptly.

3.2 Quality Assurance (QA) Personnel

  • Review and approve testing procedures and results.
  • Ensure compliance with specifications and regulatory requirements.
See also  SOP for Formulation Development of IM and SC Injections

4) Procedure

4.1 Sample Preparation

  1. Retrieve representative samples of IV injections from production.
  2. Prepare samples according to testing protocols, including dilution if necessary.

4.2 Testing Methods

  1. Perform physical tests such as visual inspection and particulate matter testing.
  2. Conduct chemical tests including pH testing, conductivity testing, and assay determination.

4.3 Microbiological Testing

  1. Perform sterility testing and endotoxin testing as per pharmacopeial or regulatory requirements.
  2. Use validated methods and controls to ensure accurate and reliable results.

4.4 Data Analysis and Reporting

  1. Analyze testing data and compare results against acceptance criteria.
  2. Document testing outcomes and report deviations or non-conformances as necessary.

5) Abbreviations, if any

QC: Quality Control
QA: Quality Assurance

See also  SOP for Disposal of Waste Materials

6) Documents, if any

  • Testing Protocols
  • Testing Records and
Reports
  • Validation Reports for Testing Methods
  • 7) Reference, if any

    USP General Chapters related to IV injections (e.g., <797>, <85>, <161>)
    FDA Guidance for Industry: Sterile Drug Products Produced by Aseptic Processing

    8) SOP Version

    Version 1.0

    Injectables Tags:Analytical method validation for injections, Aseptic media fill trials SOP, Bioburden testing for injections, Cleaning validation for injection equipment, Emulsion stability testing for injections, Formulation development for injections, Homogeneity testing for injections, IM injection SOP, Injection filling volume accuracy, Injection stability testing, Intramuscular injection procedure, Intravenous injection guidelines, IV injection SOP, Needle assembly for syringes SOP, Packaging integrity testing for injections, Particle size analysis for injections, Pre-filled syringe stability testing, Product sterility in aseptic processing, Reconstitution testing for injections, SC injection SOP, Subcutaneous injection technique, Syringe filling and capping SOP, Syringe labeling and inspection SOP, Temperature mapping in storage areas, Viscosity testing for injections

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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
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    • Injectables
    • Liquid Orals
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    • Pharmacovigilance
    • Powder & Granules
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    • 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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