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Pharmaceutical Testing And Analysis Services
13 services found
by:Materials Analytical Services, LLC (MAS) based inSuwanee, GEORGIA (US) (USA)
MAS is an ISO 17025 DEA registered cGMP laboratory. We offer accredited analytical testing services and client specified research and method development to the pharmaceutical industry. MAS tests raw materials and formulation excipients and can also implement specific compendial methods as well as perform Certificate of Analysis ...
by:Envigo based inCambridgeshire, UNITED KINGDOM
Characterisation of a biopharmaceutical product, determination of physico-chemical properties, biological activity, immunochemical properties, purity and impurities by appropriate techniques is essential for identifying the key characteristics of the product that should be considered when setting specifications for the product. These should be defined prior to conducting early clinical studies ...
Manufactured by:BCN Peptides S.A. based inSant Quintí de Mediona, SPAIN
Throughout the development and industrial lifecycle of all our APIs, we provide analytical support to contracted customers as required for cGMP compliance. We have extensive analytical expertise and offer all analytical services to ensure successful product development. Our vast platform of state-of-the-art analytical techniques is designed to meet all regulatory requirements for our products ...
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 ...
by:Broughton Laboratories based inNorth Yorkshire, UNITED KINGDOM
Broughton Laboratories Ltd. specialise in offering GMP compliant pharmaceutical testing services and our facilities are regularly inspected by the MHRA (Medicines and Healthcare Regulatory Authority). We have the ability to perform a vast array of analysis on pharmaceutical finished products, raw materials and other ingredients, ...
Manufactured by:CD Formulation based in, NEW YORK (USA)
Generally speaking, the higher the stability of the crystalline form, the higher the melting point; the difference between the melting points of two crystalline forms can be estimated relatively. CD Formulation uses hot carrier microscopy to perform melting point testing and analyze the crystalline form of a drug, which facilitates the next step in the drug development process ...
by:Gesellschaft für Bioanalytik Hamburg mbH(GBA) based inHamburg, GERMANY
In January 2012, LAT GmbH Dr. Tittel Institute for Pharmaceutical Analysis joined the GBA Laboratory Group along with its site in Gräfelfing, Bavaria. LAT GmbH offers comprehensive capabilities in the field of pharmaceutical analysis and is specialized in the following ...
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. ...
by:Eurofins Scientific based inKraainem, BELGIUM
The priority in this selection process is to achieve the safety and efficacy of a new molecular entity. The preclinical activity includes mainly safety and pharmacological testing accompanied by metabolism, bioanalysis, biomarker development and pharmaceutical analysis. Eurofins offers the whole panel of GLP-assured safety studies and a broad ...
Manufactured by:Creative BioMart based in, NEW YORK (USA)
Creative Biomart provides drug analysis service for pre-clinical drugs and natural products on their physical and chemical properties. Our services include three main assays: pre-clinical pharmaceutical property analysis, pharmacokinetics analysis & bioanalysis, andnatural product ...
by:MtoZ Biolabs based in, MASSACHUSETTS (USA)
Small molecule drugs, predominantly chemically synthesized drugs with molecular weight lower than 1000 Da. These drugs are characterized by their widespread use and mature theoretical foundations. Statistically, small molecule drugs comprise about 98% of commonly used medications. ...