Electro Farmed Azin Gostar Co
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Drug dissolution testing plays an important role in drug production and is used throughout the development process for quality control testing to assess batch stability, product release, and stability tests. In vitro dissolution testing for tablets, capsules, or other solid oral dosage forms allows for the assessment of the presence of the active pharmaceutical ingredient (API) in the active pharmaceutical ingredient formulation and is an indication of the time required for the drug substance to be released from the dose. Our scientists provide standardized dissolution testing for solid dosage products in accordance with USP (USP) 711, European Pharmacopoeia (EP) and US FDA guidelines. He is experienced in developing specific dissolution approaches that conform to released product specifications to identify changes in critical quality specifications. This includes the choice of dissolution medium, dissolution device and stirring rate. About solid dosage forms of tablets like...
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* Used in control laboratory, research and formulation unit * All variable and fixed parameters are in accordance with USP standards. * All models include: adjustable timer, displaying the number of times the basket is moved, the ability to set the number of times the basket is moved, warning of the end of the test and a separate heater. * In all models, variable parts (speed and temperature) can be calibrated. TDI2: has 2 baskets, each of which works with a completely separate control system.
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Drug dissolution testing plays an important role in drug production and is used throughout the development process for quality control testing to assess batch stability, product release, and stability tests. In vitro dissolution testing for tablets, capsules, or other solid oral dosage forms allows for the assessment of the presence of the active pharmaceutical ingredient (API) in the active pharmaceutical ingredient formulation and is an indication of the time required for the drug substance to be released from the dose. Our scientists provide standardized dissolution testing for solid dosage products in accordance with USP (USP) 711, European Pharmacopoeia (EP) and US FDA guidelines. He is experienced in developing specific dissolution approaches that conform to released product specifications to identify changes in critical quality specifications. This includes the choice of dissolution medium, dissolution device and stirring rate. About solid dosage forms of tablets like...
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Used in control laboratory, research and formulation unit All variable and fixed parameters are in accordance with USP standards. The ability to measure tablet hardness up to 500 newtons, report and record statistical calculations, has 50 memories to record tablet specifications, connect to a printer and computer and print statistical calculations, the ability to calculate based on three units of newton, kilopascal and strong cube, measurement At the same time, the diameter, thickness and hardness of the tablet * Variable parts can be calibrated in all models
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* Used in control laboratory, research and formulation unit * All variable and fixed parameters are in accordance with USP standards. * Measurement of the angle of the peak formed by the fall up to 65 degrees with a resolution of 100 degrees * Accurately measuring the pouring time and displaying hundredths of a second * Measuring the height to the tip of the drop peak and reporting the flowability quality of the powder EFL 1: with two funnels of 150 and 500 grams and cones of 30 and 40 degrees calibration