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Dissolution Test Articles & Analysis
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More are listed below: l API Physical & Chemical Characterization l Solid State Characterization of APIs l Dissolution Rate Test l Solubility Analysis l Adhesion Test l Crystallinity Determination l Particle Size Analysis l Powder Flowability Test l Determination of Contact Angle of Pharmaceutical Excipients l Cone ...
More recently, the company announced to broaden its service range to tablet fragility test, dissolution test, and disintegration test. “Staffed with a group of pharmaceutical experts specialized in chemistry, biochemistry, and engineering, CD Formulation has grown to be one of the finest contract service organizations. ...
More specifically, CD Formulation is capable of conducting the following pharmaceutical analysis services. Analysis and Testing Services Taking advantage of its extensive technical expertise in biochemistry, molecular and cell biology, chemistry, and microbiology, CD Formulation can provide comprehensive, innovative, and timely solutions to help customers quickly complete their ...
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, ...
Syringe Filters Alfa Chemistry provides high-performance sterile and non-sterile syringe filters with a wide range of membrane materials and pore sizes for sample preparation of HPLC, UHPLC, ion chromatography, dissolution testing, and other analyses. Ultrafiltration Devices Different ultrafiltration devices such as pressure-driven concentrators, protein ...
Currently, CD Formulation is capable of conducting the following pre-formulation services for pharmaceutical companies: Crystallinity Determination, Amorphous Content Determination, Hygroscopicity Evaluation, Particle Size Analysis, Moisture Content Determination, Solubility Analysis, LogP/LogD/pKa Analysis, Stability Analysis, API-Excipient Compatibility, API Physical & Chemical ...
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 ...
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 test and ...
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, ...
The solubility analysis services offered by CD Formulation aim to build a full range pH solubility profile and investigate the solubility in simulated gastrointestinal media so as to find ways to improve solubility. Besides providing dissolution profiles of active pharmaceutical ingredients in various solvents such as inorganic solvents with different pH values, organic solvents, ...
On February 25, 2021, the Organization for Economic Cooperation and Development (OECD) will hold a webinar on “Assessing the dispersion stability and dissolution (rate) of nanomaterials in the environment” to discuss the scope, content, and use of Test Guideline No. 318: Dispersion Stability of Nanomaterials in Simulated Environmental Media and its ...
The Organization for Economic Cooperation and Development (OECD) recently published two guidance documents in its series on testing and assessment: Guidance Document on Aquatic and Sediment Toxicological Testing of Nanomaterials (No. 317): The guidance document addresses practical aspects of carrying out valid tests with manufactured ...
Under high concentrations of ammonia, copper and copper alloys usually form a blue color complex indicating corrosive conditions and dissolution of the metal. This lab test shows the excellent protection against ammonia attack with Cetamine®. ...
Waters Corporation (NYSE:WAT) announced today that it has entered into an agreement with the SOTAX Group, a global developer and manufacturer of equipment for dissolution testing, automated sample preparation, and physical testing of pharmaceutical dosage forms. ...
Applications: Life-science – cell cultivation, incubating bacterial cultures, enzyme assays Industrial – textile testing, sample QC, sample mixing Biopharm – solubility testing, dissolution Food & beverage – food digestion, extractions For more information click ...
Drug release is still frequently assessed by dissolution tests – a procedure, in which the tablet is placed in a solvent with similar properties to gastric acid. ...
The 8454 UV Dissolution System is available in several scalable solutions to support both online and offline dissolution analysis. ...
(NYSE: A) today introduced the 850-DS Dissolution Sampling Station for centralizing laboratory workflow of sample transfer, filtration and collection. ...
Featuring articles on high-throughput catalysis screening, stability studies, particle size distribution, dissolution testing as well as a guest article by Confarma on the detection of pyrogens. This issue presents interesting topics like: Expanding the scope of HTS-driven development – applications to highly potent compounds and catalytic processes ...
The software supports laboratory capabilities to build, edit, search, retrieve, execute and archive all dissolution methods and test reports from a single interface. To improve efficiency, the new features allow users to: Consolidate and maintain electronic data in one location, with options for exporting information into a laboratory information management ...