Skip to content
  • Clinical Studies
  • Schedule M
  • Stability Studies
  • Pharma GMP
  • Pharma Tips
  • Pharma Books
  • Pharma Validation
  • Pharma Regulatory

SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

  • Home
  • Job Safety Analysis (JSA)
    • Oral Dosage Forms (Tablets & Capsules)
    • Oral Liquid Dosage Forms (Syrups, Elixirs, Suspensions, Emulsions)
    • Powder and Granule Dosage Forms
    • Topical Dosage Forms (Creams, Ointments, Gels, Lotions, Pastes)
    • Transdermal Dosage Forms (Patches)
  • Standard Test Procedures (STP)
  • SOP – Blog Post
  • Toggle search form

SOP for Analytical Method Development Pre-screening Studies

Posted on By

SOP for Analytical Method Development Pre-screening Studies

Conducting Pre-screening Studies for Analytical Method Development

1) Purpose

The purpose of this SOP is to outline the procedure for conducting pre-screening studies to identify potential analytical methods for further development, ensuring efficient use of resources and time.

2) Scope

This SOP applies to all personnel involved in conducting pre-screening studies for analytical method development projects within the analytical development department.

3) Responsibilities

The purpose of this SOP is to define the roles and responsibilities of all personnel involved in the pre-screening studies for analytical method development.

4) Procedure

  1. Define Screening Criteria:
    1. Establish criteria for identifying potential analytical methods based on project requirements.
    2. Consider factors such as method suitability, simplicity, and initial performance indicators.
  2. Method Identification:
    1. Identify candidate methods through literature review, internal knowledge, or previous experiences.
    2. Document the rationale for selecting each method candidate.
  3. Experimental Setup:
    1. Design and set up experiments to evaluate the initial performance of selected method candidates.
    2. Define experimental parameters and acceptance criteria for screening.
  4. Data Collection and Analysis:
    1. Collect data from pre-screening experiments and analyze method performance against defined criteria.
    2. Use statistical methods to assess initial method suitability and robustness.
  5. Selection Decision:
    1. Based on pre-screening results, decide which methods show promise for further development.
    2. Document the rationale for selecting or excluding method candidates.
  6. Documentation:
    1. Document the pre-screening study process, including screening criteria, method
identification, experimental setup, data analysis, and selection decisions.
  • Maintain records of all pre-screening study meetings and communications.
  • 5) Abbreviations, if any

    The purpose of this SOP is to define the commonly used abbreviations related to the pre-screening studies for analytical method development.

    6) Documents, if any

    List of documents to be maintained related to this SOP:

    • Screening Criteria Document
    • Method Identification Rationale
    • Pre-screening Experiment Reports
    • Method Selection Summary
    • Meeting Minutes

    7) Reference, if any

    Regulatory guidelines related to this SOP include:

    • ICH Q8: Pharmaceutical Development
    • FDA Guidance for Industry: Analytical Procedures and Methods Validation

    8) SOP Version

    Version 1.0

    See also  SOP for Analytical Method Development Risk Assessment
    Analytical Method Development Tags:Analytical method accuracy SOP, Analytical method data integrity SOP, Analytical Method Development SOP, Analytical method optimization SOP, Analytical method robustness SOP, Analytical method SOP template, Analytical method validation protocol, Analytical method validation SOP, Analytical procedure documentation, Analytical SOP example, Method development guidelines, Method development process, Method validation procedure, Method variability assessment SOP, SOP for analytical instrument qualification, SOP for analytical testing, SOP for chromatographic method, SOP for dissolution method, SOP for forced degradation studies, SOP for impurity method development, SOP for LOD and LOQ testing, SOP for method transfer, SOP for method validation, SOP for precision testing, SOP for stability indicating method

    Post navigation

    Previous Post: SOP for Formulation Development Scale-Up Studies
    Next Post: SOP for Formulation Development Pilot Batch Manufacturing

    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

    Read SOPs in your Language:

     - 
    Bengali
     - 
    bn
    English
     - 
    en
    Gujarati
     - 
    gu
    Hindi
     - 
    hi
    Malayalam
     - 
    ml
    Marathi
     - 
    mr
    Punjabi
     - 
    pa
    Tamil
     - 
    ta
    Telugu
     - 
    te

    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.

    Copyright © 2025 SOP Guide for Pharma.

    Powered by PressBook WordPress theme

    Go to mobile version