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Illicit Tablet Analysis Using Raman Spectroscopy
Raman spectroscopy can be used for the analysis of prescription, counterfeit, and designer drug tablets in just minutes with little to no sample preparation. As part of the presentation we will make our debut presentation of the new Law...
Webinar: Near-Infrared Analysis in the Pharmaceutical Manufacturing Process
Webinar: Near-Infrared Analysis in the Pharmaceutical Manufacturing Process Please join us for our webinar: Near-Infrared Analysis in the Pharmaceutical Manufacturing Process.   Monitoring the quality of a manufacturing process...
Webinar: Stationary Phase and Mobile Phase Selection for Hydrophilic Interaction Liquid Chromatograp
Stationary Phase and Mobile Phase Selection for Hydrophilic Interaction Liquid Chromatography   Date: 11th July, 2012Time: 8:00am PST / 11:00am EST / 4:00pm UK / 5:00pm CET What Does it Cover Hydrophilic...
Ensuring Product Quality with Spectroscopy Techniques (Pharmaceutical Industry)
Ensuring Product Quality with Spectroscopy Techniques (Pharmaceutical Industry)During a solid-dosage manufacturing process in pharmaceutical companies, quality control is done in every step of the process to ensure final product quality....
Infrared and UV-Vis Spectroscopy in Pharmaceutical QC - Part 2:  Ensuring Product Quality
Infrared and UV-Vis Spectroscopy in Pharmaceutical QC - Part 2:  Ensuring Product Quality Thursday, June 14, 2012Session 1 - 9 a.m. EDT/13:00 UTC/GMTSession 2 - 4 p.m. EDT/20:00 UTC/GMT During the pharmaceutical manufacturing...
Webinar: Infrared and UV-Vis Spectroscopy in Pharmaceutical QC - Part 1:  Regulatory Considerations
Infrared and UV-Vis Spectroscopy in Pharmaceutical QC - Part 1:  Regulatory Considerations Ensuring compliance with regulatory requirements for pharmaceutical and medical device manufacturers is essential for delivering safe and...
Webinar: Increased Throughput for Trace Impurities and Residual Solvent  Determination with Unattend
US Pharmacopeia (USP) method <467> details the procedures for the identification, control and quantification of Class 1 and Class 2 residual solvents through the use of headspace gas chromatography. Some pharmaceutical laboratories...
Smarter FT-IR Spectroscopy for Pharmaceuticals
The Nicolet iS50 is a fully integrated system that provides a unique foundation for new drug development, production support or the analytical services laboratory. It not only provides state-of-the-art FT-IR spectroscopy with a integrated...
Analysis of Residual Solvents using GC/FID with Headspace and a Cyanopropylphenyl Polysiloxane Phase
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