Good Laboratory Practices (GLP) Part-2 - Pharmaguideline
Good Laboratory Practices (GLP) Part-2 - Pharmaguideline
• Dissolution
Ø Ensure that the apparatus is in the calibrated state before use.
Ø Before start of the analysis, ensure cleanliness of dissolution bath. Check the physical calibration like RPM, the distance shaft from the center
of jar, the integrity of basket mesh etc.
Ø Check the temperature of dissolution medium before and after dissolution analysis by using a thermometer.
Ø Use calibrated accessories for checking physical parameters.
Ø Weigh the tablets / capsules before adding in the dissolution medium.
Ø Ensure that the dissolution medium is degassed before use & check previous product cleanliness.
Ø After completion of the specified time interval of the dissolution test physically check for the appearance of the content in the dissolution bowl
whether there is any lump formation / non-disintegration of the tablet or capsule / or any other irregular observation.
• Titration
Ø Before start of analysis ensures that the correct volumetric solution with correct morality is used.
Ø Before start of the analysis, molarity should be checked by the second person.
Ø Ensure that the molarity of solution is valid while performing the titration
Ø Use correct indicator and ensure its validity.
Ø Cautiously determine the endpoint when it is the visual determination of endpoint.
Ø For potentiometric titration ensure that the reference solution is available in the electrode.
Ø Properly condition the electrode and regenerate the electrode if required.
Ø After completion of analysis store electrode in its respective solution.
• Conductivity meter
Ø Ensure that the instrument is in calibrated condition before use.
Ø Ensure all the connections of the instrument are proper before use.
Ø Ensure the correct electrode is connected to the instrument and is properly cleaned and stored.
Ø Ensure that the temperature sensor is connected to the instrument.
Ø After use wash the electrode and temperature probe with water and wipe neatly with tissue paper. Then immerse the electrode and
temperature probe sufficiently deep in the beaker containing sample solution.
Ø Make the relevant entries in the instrument log book after using the instrument.
Ø Calibrate the instrument daily.
Ø If the electrode constant “K” is out of limit, Calibration shall be repeated by preparing a fresh standard solution.
Ø Even after recalibration, If the electrode constant “K” lies out of limit, the probe should be reactivated by replatinizing (done by an external
party).
Ø After rechecking if an acceptance criterion is not met, then replace the electrode.
Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of Pharmaceutical Guidelines, a widely-read
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