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Pharmaceutical Disintegration Test Services In Usa New York
8 services found
Manufactured by:CD Formulation based inShirley, NEW YORK (USA)
The heat shrinkage rate of the film is directly related to the aesthetics of the film. In the packaging process, the film must be flat and tightly fitted to the surface of the goods without wrinkles. CD Formulation can provide customers with heat shrinkage rate testing of plastic films to ensure the shape and dimensional accuracy of the products. Learn more at ...
Manufactured by:Alfa Chemistry based inNY, NEW YORK (USA)
The detection of microbial limit is one of the important measures to ensure its quality and drug safety. T,C&A Lab runs strictly in accordance with GMP and GLP standards to meet the relevant requirements of compliance, quality, efficiency, etc. We can perform microbiology testing according to USP , and . Welcome to contact our experts for consultation. Learn more atbout Pharmaceutical ...
Manufactured by:Alfa Chemistry based inNY, NEW YORK (USA)
The stability of pharmaceutical products refers to the ability of APIs and preparations to maintain their physical, chemical, biological and microbiological properties. The purpose of stability study is to investigate the changes of the properties of APIs or preparations with time under the influence of temperature, humidity, light and other conditions, so as to provide a scientific basis for the ...
Manufactured by:CD Formulation based inShirley, NEW YORK (USA)
Loss-on-drying (LOD) is determined by heating a sample in an oven to a temperature below its melting point and includes all volatile substances, including water content and solvents. CD Formulation provides loss-on-drying testing to determine the amount of volatile substances in tablets, capsules or bulk materials. CD Formulation offers a one-stop service for testing the physical and chemical ...
Manufactured by:CD Formulation based inShirley, NEW YORK (USA)
The main features of the melting time limit tester are: three metal frames can be reversed automatically and synchronously according to the operation mode set by the user, a unique automatic ascending and manual turning method is adopted to ensure easy use and cleaning of the test vessel, constant temperature water circulation to reach ≤ ± 0.1 accuracy, automatic temperature control, automatic ...
Manufactured by:CD Formulation based inShirley, NEW YORK (USA)
The residue on ignition check method is used as an indicator to control the quality of API. CD Formulation offers a professional drug residue on ignition test, which assesses the quality of a drug by heating the drug to char and then ashing it. CD Formulation's business covers all aspects of drug formulation, drug ingredients, drug development, drug testing, drug optimization, etc. ...
Manufactured by:CD Formulation based inShirley, NEW YORK (USA)
The purpose of CD Formulation's headspace analysis tests for pharmaceutical packaging is to detect the residual gas content in pharmaceutical packaging and to adjust the packaging process accordingly. The residual gases inside the package should not be disregarded at the end of the packaging process. It is very difficult to control and change the gas content inside the package from the end of ...
Manufactured by:Alfa Chemistry based inNY, NEW YORK (USA)
The purpose of pharmaceutical testing is to prevent substandard pharmaceuticals from entering the market and ensure the safety of pharmaceuticals. T,C&A Lab provides analysis and testing services for a wide range of products from raw materials to finished products in the pharmaceutical and biopharmaceutical industries. Raw materials, intermediate products and by-products Finished products ...