SOP for Trend Analysis | Pharmaguideline
  •   Pharmaguideline Courses Start Learning
  • Apr 17, 2021

    SOP for Trend Analysis

    Standard operating procedure to prepare the trend for analysis of different test results for tablet, capsule and liquid samples.

    1.0 OBJECTIVE

    To lay down the procedure for Trend analysis.

    2.0 SCOPE

    This SOP shall be applicable to Quality Control Dept.

    3.0 RESPONSIBILITY

    Supervisor Quality Control

    4.0 ACCOUNTABILITY

    Sr. Manager Quality Assurance

    5.0 PROCEDURE

    5.1 Trend analysis shall be carried out for all batches of key products manufactured in a year.
    5.2 List out all the important tests mentioned below which are likely to reflect on the process parameters.
    Tablet: Assay, Uniformity of content, Dissolution if applicable, Impurity profile (if any) and yield.
    Capsule: Assay, Uniformity of content, Dissolution if applicable and Impurity Profile (if any) & Yield.
    Liquid: Assay, Fill volume, pH, Specific gravity and Yield.
    5.3 Report in a tabular form all the values under each test.
    5.4 Calculate average value, minimum value and maximum value.
    5.5 Calculate Standard Deviation and Relative Standard Deviation (RSD) for assay.
    5.6 The RSD of the observed assay and Content uniformity values shall not exceed 4%.
    5.7 Significant deviation if any shall be investigated by Sr. Manager Quality Assurance in consultation with General Manager Technical Operation and documented in Trend Analysis report.
    5.8 Corrective actions, if required, shall be taken in consultation with Production, Research and Development, Maintenance, and Quality Assurance department as the case may be.
    5.9 The Trend Analysis report will be complied with Annual Product Review record and sent to General Manager Technical Services.
    5.10 If outside vendor is selected for trend analysis, inform the findings to the concerned vendors.
    5.11 If significant deviations are observed, conduct a fresh audit by Quality Assurance at the premises of the supplier.
    5.12 Inform General Manager Technical Services about the observations and action required (if any).

    6.0 ABBREVIATIONS

    6.1 SOP: Standard Operating Procedure
    6.2 QA: Quality Assurance
    6.3 QC: Quality Control
    6.4 Dept.: Department
    6.5 RSD: Relative Standard Deviation
    Get editable documentsView List

    No comments:

    Post a Comment

    Please don't spam. Comments having links would not be published.


    Popular Categories ๐Ÿท️

    QA SOPs QC SOPs Micro SOPs HVAC Production SOPs Stores SOPs Checklists Maintenance SOPs HPLC Sterile GLP Validation Protocols Water System GDP Regulatory Maintenance Calibration Warning Letters Education B.Pharmacy
    Online Courses Salary Calculator
    Follow on Whatsapp


    Certificate Courses ๐ŸŽ–️

    Pharmaceutical Courses

    Follow Pharmaguideline


    DOCUMENTS ๐Ÿ“‹

    PHARMACEUTICAL DOCUMENTS




    Editable Pharmaceutical Documents in MS-Word Format. Ready to use SOPs, Protocols, Master Plans, Manuals and more...

    View


    adsbypg


    GET APP FOR NEWS UPDATES


    Android App