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SOP for Formulation Development Analytical Method Development

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SOP for Formulation Development Analytical Method Development

Developing Analytical Methods in Formulation Development

1) Purpose

The purpose of this SOP is to outline the procedure for developing analytical methods during the formulation development process, ensuring robust methods for assessing product quality and performance.

2) Scope

This SOP applies to all formulation development projects within the organization, covering analytical method development activities from method selection to validation and implementation.

3) Responsibilities

The responsibilities for this SOP include:
Project Manager: Overseeing analytical method development activities and ensuring alignment with project objectives and timelines.
Analytical Development Scientist: Conducting method development experiments and optimizing analytical techniques.
Quality Assurance: Reviewing and approving method development protocols, validation plans, and final method validation reports.
Regulatory Affairs: Ensuring analytical methods meet regulatory requirements and supporting submissions.

See also  SOP for Formulation Development Pre-formulation Studies

4) Procedure

4.1 Method Selection and Feasibility Study

  1. Identify analytical requirements based on product characteristics, regulatory guidelines, and intended use.
  2. Conduct literature review and feasibility studies to select appropriate analytical techniques.
  3. Assess method feasibility in terms of sensitivity, specificity, accuracy, precision, and robustness.

4.2 Method Development

  1. Design experimental protocols for method development, including experimental design and acceptance criteria.
  2. Optimize analytical parameters (e.g., mobile phase composition, detection wavelength) to achieve desired method performance.
  3. Document method development activities, results, and rationale for method selection.

4.3 Method Validation

  1. Develop a
validation protocol outlining validation parameters, acceptance criteria, and experimental procedures.
  • Validate analytical methods according to International Conference on Harmonisation (ICH) guidelines or applicable regulatory standards.
  • Perform validation experiments, including specificity, linearity, accuracy, precision, and robustness studies.
  • 4.4 Method Transfer and Implementation

    1. Transfer validated methods to quality control or analytical testing laboratories as applicable.
    2. Provide training to analysts on the use and application of developed and validated analytical methods.
    3. Verify method performance and suitability in routine analysis through method verification studies.

    4.5 Method Documentation and Reporting

    1. Prepare comprehensive method development and validation reports summarizing experimental data, results, and conclusions.
    2. Obtain review and approval of method development and validation reports from designated approvers.
    3. Archive final method validation reports and related documentation for future reference and regulatory inspections.

    5) Abbreviations, if any

    SOP: Standard Operating Procedure
    ICH: International Conference on Harmonisation

    6) Documents, if any

    Method Development Protocols
    Validation Protocols and Reports
    Method Transfer Documents
    Method Validation Summaries

    7) Reference, if any

    – ICH Q2(R1): Validation of Analytical Procedures: Text and Methodology
    – FDA Guidance for Industry: Analytical Procedures and Methods Validation for Drugs and Biologics

    8) SOP Version

    Version 1.0

    See also  SOP for Formulation Development Process Validation
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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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