Standard Operating Procedure for preparation & standardization of volumetric solution

  1. OBJECTIVE:

To lay down a procedure for preparation & standardization of volumetric solution.

  • SCOPE:

This procedure is applicable for procedure for preparation & standardization of volumetric solution.

  • RESPONSIBILITY:

QC Officer/ QC Executive

  • ACCOUNTABILITY:

QC Manager.

  •  PROCEDURE:
    • General Instructions:
      • All chemicals / solvents used for preparation of volumetric solutions and reagents shall be LR Grade / AR Grade.
      • All volumetric solutions / reagent shall be prepared in purified water or distilled water.
      • Prepared the Volumetric Solution  and determine the normality of volumetric solution.
    • Preparation & Standardization of Volumetric Solutions:
      • All volumetric solutions/reagents shall be freshly prepared weekly, once in 15 days, once in every month/ three months or whenever the solution shows any fungal growth or sedimentation and deviation of the strength [Molarity /Normality] from the desired value not more than ± 10%.
      • Preparation of volumetric solution is documented.
      • Re-standardize the Volumetric solutions as per the following frequency or before use whichever is later.
      • Records will be maintained in the Volumetric Solution Standardization Record.
      • Standardization shall be determined in triplicate either by manually or potentiometrically (wherever applicable). Strength of volumetric solution shall be within ± 10.0 % of the specified strength. Record shall be maintained.
      • Code sequence of volumetric solution QC/VS/000-00.
        • Where QC is Quality Control.
        • Where VS is Volumetric Solution
        • Where 000 is ID No. Volumetric Solution.
        • Where 00 is mention for no. of determination of normality of Volumetric Solution.
      • Store all volumetric solutions / reagents in borosilicate stopper glass bottle, protected from heat, air & moisture. Volumetric solutions / reagents shall be stored in amber/transparent stopper glass bottles.
      • Standardization of volumetric solution should be standardize ± 1 days from due date of standardization.
      • Label the volumetric solutions status label.
      • After use the volumetric solution should be mention volume of volumetric solution.
      • Record maintain of primary standard during use of primary standard; determine the normality of volumetric solution.
      • Affix the label on primary standard.
      • Prepared the list of primary standard.
  • TRAINING:

Trainer   : Manager – Quality Control

Trainees : Staff of the QC departments

  • DISTRIBUTION:

Master Copy                  :           QA Department

Controlled Copy            :           QC Department

Display Copy                 :           QC Department

  • REFERENCES:

In-House

Bhanu Pratap Singh

BHANU PRATAP SINGH IS EXPERIENCED IN PHARMACEUTICAL, AUTHOR AND FOUNDER OF PHARMACEUTICAL GUIDESLINE (WWW.PHARMAGUIDESLINE.COM), A WIDELY READ PHARMACEUTICAL BLOG SINCE 2019. EMAIL:- INFO@PHARMAGUIDESLINE.COM

View all posts by Bhanu Pratap Singh →

Leave a Reply

Your email address will not be published. Required fields are marked *

error: Content is protected !!