Refine by
Cd Formulation Pharmaceutical Microbiology Testing Services
5 services found
Manufactured by:CD Formulation based in, 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:CD Formulation based in, 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 in, 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 in, 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 in, 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 ...