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Microbial Limits Test Articles & Analysis

9 news found

CD Formulation: Advancing Pharmaceutical Analysis and Testing through Biological Determination

CD Formulation: Advancing Pharmaceutical Analysis and Testing through Biological Determination

During this process, direct inoculation and membrane filtration methods are used. Microbial Limits TestAnother critical test for pharmaceutical products is the microbial limits test. ...

ByCD Formulation


CD Formulation Strengthens Its Role as a CRO Company for Pharmaceuticals   

CD Formulation Strengthens Its Role as a CRO Company for Pharmaceuticals  

The pre-formulation service provided by CD Formulation includes Crystallinity Determination, Amorphous Content Determination, Hygroscopicity Evaluation, Particle Size Analysis, Moisture Content Determination, Solubility Analysis, API-Excipient Compatibility, API Physical & Chemical Characterization, Dissolution Rate Test, Solid State Characterization of APIs, Powder ...

ByCD Formulation


CD Formulation Provides Comprehensive Formulation Development and Analytical Services for the pharmaceutical Industry

CD Formulation Provides Comprehensive Formulation Development and Analytical Services for the pharmaceutical Industry

Drug Analysis To ensure the drug meets the regulatory requirements, drug analysis is necessary during which process physical, chemical, or biological methods are used to test and analyze different dosage forms of drugs. CD Formulation provides the following drug analytical services: Disintegration Test, Dissolution Test, Tablet Hardness ...

ByCD Formulation


STEMart Launches Microbiology & Sterility Testing Services for Medical Devices

STEMart Launches Microbiology & Sterility Testing Services for Medical Devices

Sterilization is the process of removing microorganisms. Sterility testing is defined as microbial testing applied to sterile products in order to demonstrate that the product is manufactured and processed according to cGMP-guided practices or to confirm whether the product is sterile or not. ...

BySTEMart


CD Formulation Provides Moisture Content Determination for Drug Formulation and Analysis

CD Formulation Provides Moisture Content Determination for Drug Formulation and Analysis

Moisture testing is viewed as one of the most fundamental quality parameters to ensure drug stability. ...

ByCD Formulation


CD Formulation Releases Moisture Content Determination for Drug Develoment and Analysis

CD Formulation Releases Moisture Content Determination for Drug Develoment and Analysis

Moisture testing is viewed as one of the most fundamental quality parameters to ensure drug stability. ...

ByCD Formulation


CD Formulation Optimizes Elemental Impurities Analysis Service

CD Formulation Optimizes Elemental Impurities Analysis Service

Previously, the company has already released a wide array of drug analytical services, covering bioavailability/bioequivalence detection, disintegration test, dosage unit uniformity test, microbial limits test, tablet fragility test, dissolution test, tablet hardness ...

ByCD Formulation


CD Formulation Launches a Full Range of Drug Analysis Services for the Pharmaceutical Industry

CD Formulation Launches a Full Range of Drug Analysis Services for the Pharmaceutical Industry

Earlier this month, the company announced that a full range of drug analysis services are now available for clients across the globe who are engaged with new drug development. The analytical testing of pharmaceutical products involves chemical, physical and sometimes microbiological analysis. “More specifically, this process involves aspects of identifying novel drugs, ...

ByCD Formulation


CD Formulation Offers Multiple Methods for Microbial Limit Test

CD Formulation Offers Multiple Methods for Microbial Limit Test

As an expert specializing in drug formulation, CD Formulation announces to release microbial limit test (MLT) service for drug development projects to determine whether a non-sterile pharmaceutical product complies with the established specifications. ...

ByCD Formulation

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