Qualification of Dissolution Testers USP Performance Verification Test (PVT)

  Рет қаралды 12,390

US Pharmacopeia

US Pharmacopeia

Күн бұрын

Пікірлер: 8
@ds3718
@ds3718 Жыл бұрын
Please share updated dissolution calibration procedure..
@matchmedicines8209
@matchmedicines8209 2 жыл бұрын
thanks for the perfect explanation🙏🏻 I have a question, is it necessary to do the disintegration test before the dissolution test?
@shifaeqalb6661
@shifaeqalb6661 2 жыл бұрын
is there active limit mention in guideline ? how much active atleast should be present in tablet for dissolution test requirement? if tablet contain 5 or 25 mg active ingredient should we perform dissolution test on it or not require?
@nn-yl6bd
@nn-yl6bd 3 жыл бұрын
I do thank you for sharing this🌷
@aniketsingh1371
@aniketsingh1371 3 жыл бұрын
Sir, can you please tell me about the use of chlorpheniramine tablets in USP apparatus type 3? is it removed from USP as I could not find any source of access. pp
@takeshiinoue4105
@takeshiinoue4105 2 жыл бұрын
Chlorpheniramine Maleate ER Tablets RS was announced to be discontinued on December 20, 2012. The 30 dips per minute test is no longer required in the Performance Verification Test for USP Instrument 3.
@takeshiinoue4105
@takeshiinoue4105 2 жыл бұрын
Effective February 1, 2012, USP has removed the requirement for Apparatus 3 Performance Verification Test Apparatus Suitability section of General Chapter Dissolution. The change was necessary because the supply of current lot G1J218 has been depleted and no suitable replacement has been found.
@pmman4232
@pmman4232 2 жыл бұрын
Is this channel legit?
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