Farmaceutika i biotehnologija Learning centri: Pharma & Biopharma Learning Center Brošure i aplikacije: Ion Chromatography for Pharma and Biopharma Brochure: Q Exactive BioPharma – The Complete BioPharma Characterization Solution Why switch to Chromeleon CDS now? Biopharmaceutical Analytical Testing Peptide Mapping § Peptide Mapping Information · Download peptide mapping workflow › o Digestion § Download brochure § Read protein digestion eBook § Calculate digestion time § Video: SMART Digest Kit Animation § Webinar: Take the Smart Route to Protein Digestion o Peptide separation § Read application § Webinar: Peptide Separations with Pinpoint Precision § Find out more about how the Vanquish Flex is built for biopharma o Peptide mass spectrometry Read brochure Read poster note Webinar: Don’t Miss a Thing on Your Peptide Mapping Journey Peptide mapping software Download brochure (PDF) Find out more on Planet Orbitrap Video: Learn about CDS Glycan Analysis Glycan Analysis for Biotherapeutics Biopharmaceutical Characterization Application Compendium Liquid Chromatography Columns for every Biopharmaceutical Analytical Workflow Intact Glycoform Analysis Unlabeled Glycan Workflow Glycopeptide Workflow Monosaccharide and Sialic Acid Workflow Intact Protein Analysis Workflows § Intact Mass Analysis § Charge Variant Analysis § Protein Aggregation Analysis § Sub-Unit Mass Analysis § Native Intact Mass Analysis § Titer (Affinity) Analysis § Orbitrap MS – Built for BioPharma Hydrogen deuterium exchange (HDX) workflow § Download brochure Optimization of a Fully Automated Hydrogen/Deuterium Exchange Mass Spectrometry Platform for Probe Protein Conformation/Conformation Dynamics Characterization of the Conformation of Therapeutic Antibody Oxidation Variants with Optimized Hydrogen/Deuterium Exchange Mass Spectrometry Higher Order Protein Stucture Elucidation by HDX-MS Optimizing Electron Transfer Dissociation Conditions for Hydrogen/Deuterium Exchange Mass Spectrometry and Its Application to the Study of Protein Conformation Antibody Drug Conjugates (ADCs) § MAbPac HIC-Butyl Columns § MAbPac SEC-1 Columns § MAbPac SEC-1 Columns Quick Start Guide § Brochure: Q Exactive BioPharma – The Complete BioPharma Characterization Solution § BioLC Columns – Innovative Solution for mAb Analysis and Characterization Oligonucleotide and Amino Acid Analysis § DNAPac PA200 and PA200 RS Columns § DNAPac PA200 RS 4?m Columns § Brochure: DNAPac Family of Columns – Superior Oligonucleotide Analysis § High Resolution LC/MS Analysis of Therapeutic Oligonucleotides on a New Porous Polymer-based Reversed Phase Column Biosimilar Analysis Workflows § Monosaccharide and Sialic Acid Determinations in Biosimilars Using HPAE-PAD § BioPharma Charge Variant & Aggregate Analysis eBook Poster Note: Structure Characterization and Differentiation of Biosimilar and Reference Products Using Unique Combination of Complementary Fragmentation Mechanisms Poster: Differentiate Minor Difference of Protein Structure in Biosimilar and Reference Products Using High-Resolution Orbitrap LC-MS/MS Elemental Impurities § Download brochure Download ICP-OES Brochure Read application: Analysis of elemental impurities in drug products using ICP-OES Application note: Mercury impurities in Pharmaceuticals Analysis of Pharmaceutical Products for their Elemental Impurities with the Thermo Scientific iCAP RQ ICP-MS Frequently asked questions (FAQs) about the analysis of elemental impurities in pharmaceutical drug products Volatile Organic Impurities and Residual Solvents · AppsLab Library Methods for Residual Solvents Analyzing Residual Solvents in Pharmaceutical Products Using GC Headspace with Valve-and-Loop Sampling Improving Pharmaceutical Laboratory Throughput in the Analysis of Trace Impurities and Residual Solvents with Liquid/Headspace Unattended Switching and Automated Standard Preparation Semi-Volatile Organic Impurities Application: Impurity Profiling of Pharmaceutical Starting Materials Using Gas Chromatography Coupled with High-Resolution Accurate Mass Spectrometry Webinar: Pharmaceutical Impurity Profiling: Simple, Confident Analysis with New GC-MS Technology Applicability of gas chromatography/quadrupole-Orbitrap mass spectrometry in support of pharmaceutical research and development Confident Identification of Leachable Impurities from Pharmaceutical Container Closure Materials using OrbitrapMass-Spectrometer-Based GC-MS Non-Volatile Organic Impurities Effective Workflow for Pharmaceutical API Impurity Analysis using HR- LCMS and Compound Discoverer Metoprolol and Select Impurities Analysis Using a Hydrophilic Interaction Chromatography Method with Combined UV and Charged Aerosol Detection Fast Nevirapine Impurity Profiling Using UHPLC-DAD Orbitrap Fusion Tribrid Mass Spectrometer for Pharmaceutical Impurity Analysis A Sensitive Method for Direct Analysis of Impurities in Apramycin and Other Aminoglycoside Antibiotics Using Charged Aerosol Detection Counterion Analysis Determination of Inorganic Counterions in Pharmaceutical Drugs Using Capillary IC Part A Determination of Inorganic Counterions in Pharmaceutical Drugs Using Capillary IC Part B Fast Separations of Counter Ion in an Allergy Drug Tablet Using High-Pressure Capillary IC Extractables and Leachables Extractables and Leachables Brochure Accelerated Solvent Extraction of Extractables from Polymeric Components Used in Precision Drug Delivery Devices Comparison of Soxhlet and Accelerated Solvent Extraction for Leachable and Extractable Analysis of Packing Material Accelerated Solvent Extraction for Additives in Polymer Materials Confident Identification of Leachable Impurities from Pharmaceutical Container Closure Materials using OrbitrapMass-Spectrometer-Based GC-MS Pharmaceutical Quality Control Testing Pre-Clinical and Clinical Drug Testing Large Molecule Bioanalysis/DMPK Webinar: How to improve your peptide quantitation workflows Optimization of Orbitrap Acquisition Parameters for Quantitative Bioanalysis Confident quantitation for small and large molecule bioanalysis
