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Month: November 2022

2022 Final Program & Abstract Book

November 9, 2022

–

dave

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Thanks to all who made EAS 2022 a success! Follow the link to download our programs.
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E13 – Dissolution: A Rational Approach
E13 – Infrared Spectral Interpretation
E13 – Leachables and Extractables
E13 – NMR: Basic Theory, Sprectral Interpretation and Applications
E13 – Physical Characterization and Analytical Test of Pharma Solids 1
E13 – Physical Characterization and Analytical Test of Pharma Solids 2
E13 – Physical Characterization and Analytical Test of Pharmaceutical Solids I & II
E13 – Practical Headspace Gas Chromatography
E13 – Practical, Scientific use of Photogrammetry and Structure from Motion Technologies in Cultural Heritage organized by NYCF
E13 – Qualification of Analytical Instruments for the Pharmaceutical Laboratory
E13 – Quality Control of Small Molecule Drugs
E13 – Quantitative Lab Skills for the Modern Analyst
E13 – Small Molecule Single Crystal X-Ray Crystallography in Structural Chemistry
E13 – The Art of Managing a High Performance Lab
E14 – Quality-by-Design: A New Paradigm for the Analytical Laboratory II
E14-02: Essentials of Modern HPLC/UHPLC Part I & II
E14-03: Principles of Trace Level Structure Elucidation
E14-14: Essentials of Modern HPLC/UHPLC 2
E14-24: Infrared Microspectroscopy and Chemical Mapping at the Nanoscale
E15-06: Physical Characterization & Methods of Analysis Part 1 & 2
E15-13: Handheld Instruments
E15-16: Developing, Validating and Troubleshooting Dissolution Methods
E15-26: Drug Quality Fundamentals Part I & II
E15-27: Drug Quality Fundamentals Part 1
E15-28: Drug Quality Fundamentals Part 2
E15-29: Atomic Spectrometry
E15-35: Making the Transition to GC-MS, GC-MS-MS and GCxGC-MS
E15-36: Quality-by-Design (QbD) Fundamentals for Analytical Chemists: A New Paradigm for the Analytical Laboratory
E16-11: Analysis of Proteins and Peptides in Biological Matrices by LC-MS/MS
E16-13: Polymers: An Introduction and Characterization Techniques
E16-15: Science, Risk and Statistics in Cleaning Validation
E16-17: Analytical Forensic Metrology
E16-26: Sample Preparation: The Chemistry Behind the Techniques
E16-27: Conducting Effective Investigations of Out of Specification and Atypical Laboratory Results
E16-28: CounterCurrent Chromatography (CCC)
E16-30: Practical Guide to Reversed-Phase HPLC
E16-33: Fundamentals and Practical Applications of Laser-Induced Breakdown Spectroscopy
E16-34: Practical Introduction to Titration Method Development
E16-35: Hands-on FT-IR Microspectroscopy
E16-36: Introduction to Gas Chromatography/Infrared Spectroscopy
E17-11: Introduction to Atomic Force Microscopy (AFM) for Industrial Applications
E17-12: Introduction to Basic Light and Electron Microscopy for Pharmaceutical Industry Quality Scientists
E17-13: Analytical Development for Generics and Over-the-Counter Products
E17-17: Process Analytical Technology (PAT)/Quality by Design (QbD): Enhancing Effectiveness in the Analytical Laboratory
E17-19: Update on New Analytical Requirements of USP General Chapters
E17-25: Intro to GLP Regulations and Bioanalytical Method Validation by LC-MS/MS
E17-26: A Systematic Way for Analytical Chemists to Prepare for a Quality Audit or Regulatory Inspection
E17-29: Intro to Drug Discovery/Development Process
E17: Impurities in Pharmaceuticals – A Survey Course
E17: The Chemistry of Drug Degradation
E18-09: Introduction to Vibrational Spectroscopy for Real Time Analysis
E18-13: Develop Robust HPLC Methods for Pharmaceutical Analyses
E18-17: Optimizing HPLC Separations Using Knowledge of Analyte Size, Particle Pore Size and Phase Chemistry
E18-18: Taking Advantage of the Power in Excel
E18-21: Evaluation of Trace/Ultratrace Impurities in Pharmaceuticals
E18-30: Stability Studies: The Tools, Methods and Predictions During Each Stage of Pharmaceutical Development
E18-31: Setting Data Quality Objectives and Determining, Reporting, and Interpreting Data Quality Indicators to Meet Scholarly Publication Requirements
E18-36: Analytical Instrument Qualification from a Chemical Metrology Perspective
E19-01: LC/MS: Theory, Instruments and Applications
E19-10: Physical Characterization of Pharmaceuticals and Biopharmaceuticals Using Synchrotron Methods
E19-12: Faster HPLC Method Development and Optimization of Polar and Nonpolar Analyte Mixtures
E19-13: Effective Utilization of PDA and MS Data in LC and SFC Method Development
E19-14: Polymers: An Introduction and Characterization Techniques
E19-18: Interpretation of Mass Spectra with Practical Solutions to Problems
E19-21: Process Analytical Technology (PAT) and Quality by Design (QbD) Integration for Effectiveness in the Analytical Laboratory
E19-25: Quality-by-Design: A New Paradigm for the Analytical Laboratory Part 1 & 2
E19-33: Design of Experiments for Analytical Chemists: Key to Effective Quality-by-Design Laboratory Operation
E19-35: HPLC and UPLC troubleshooting
E19-39: The Chromatographic and Spectroscopic Tools of an Analytical Chemist for Measuring Polycyclic Aromatic Compounds in Complex Samples
E2-08: High-Performance Thin-Layer Chromatography an Alternative Approach to Quality: Standardization, Quantification and Automation
E20-10: Raman Microscopy Imaging
E20: A Practical Introduction to Infrared, Raman, and Near Infrared Spectroscopy
E20: Concepts in Pharmaceutical Impurity Analysis
E20: Life Cycle Management of Analytical Validation for Pharmaceutical Products
E20: Machine Learning for Chemometricians: ANNs, SVMs, XGBoost and other Non-linear Methods for Calibration and Classification
E20: Modern Size Exclusion Chromatography of Synthetic Polymers and Biopolymers
E21-02: Practical Gas Chromatography
E21-03: Basic Mass Spectrometry
E21-12: History, Environmental Issues, and Characterization of Microplastics
E21-20: Intellectual Property Fundamentals for Scientists
E21-21: Atomic Spectroscopy in the Pharmaceutical Laboratory
E21-23: Cancelled
E21-25: GC/MS Fundamentals for Operators
E21-26: Communicating Analytical Results in the Pharmaceutical Labs and Understand Human Errors in Maintaining Data Integrity
E21-28: Protein Therapeutics Immunogenicity
E21-30: R Programming for Analytical Chemistry
E21-31: Cannabis Lab Essentials: Understanding the Cannabis Landscape and the Critical Process of Test Method Development and Validation
E21-35: Headspace-Gas Chromatography Fundamentals, Method Development and Method Transfer
E21-36: Safety in the Laboratory
E21-37: Uniting Analytical Technologies – TGA-IR-GCMS, LC-ICP-MS
E21-38: Sample Processing, Preparation, and Analysis the QuEChERSER Way
E21: HPLC & UHPLC for Practicing Scientists Part 1: Fundamentals
E21: HPTLC – The Other High-Performance Chromatography: Parameters, Applications, Method Development and Troubleshooting
E22-04: Chemometrics without Equations Parts 1 & 2
E22-11: Process Analytical Technology: Out of the Lab and into the Line
E22-16: Lifecycle Approach to Analytical Methods for Drug Products, Incorporating QbD Concepts
E22-18: How to Develop Validated HPLC Methods: Rational Design with Practical Statistics & Troubleshooting
E22-21: Analytical Challenges of Emerging Contaminants for Young Research Professionals
E22: Characterization of Biologics by HPLC, CE, and Mass Spectrometry
E22: HPLC and UHPLC for Practicing Scientists 1 and 2: Fundamentals, Method Development, and Troubleshooting
E22: Intermediate Chemometrics without Equations
E23-02 HPLC and UHPLC for Practicing Scientists Part 1 ONLY: Fundamentals
E23-02: HPLC & UHPLC for Practicing Scientists Part 1: Fundamentals
E23-03: Sample Preparation: The Chemistry Behind the Techniques
E23-08: Practical LC-MS Method Development and Sample Preparation
E23-09: Non-Linear Machine Learning for Calibration and Classification
E23-12: Green Analytical Chemistry
E23-13: HPLC and UHPLC for Practicing Scientists Part 2 ONLY: Applications, UHPLC, Method Development, and Troubleshooting
E23-15: Intact and Top-Down Protein Characterization and Quantitation by Mass Spectrometry: Approaches for Pharmaceutical Drug Discovery, Development, and Bioanalysis
E23-16: Design of Experiments (DoE): Key to Effectiveness and Continuous Improvement in the Laboratory
E23-17: Practical LC-MS/MS Method Validation for Practical Scientists
E23-18: Improve Your LC Separations – What to Do Next When C18 Does or Doesn’t Work
E23-19: Practical Raman Microscopy
E23-21: Two-Dimensional Liquid Chromatography for Pharmaceutical Analysis
E23-23: Problems with FT-IR Spectra and How to Avoid Them
E23-25: The Importance of Microscopy in Microspectroscopy
E23-26: Process Analytical Technology: Out of the Lab and into the Line
E23-27: Introduction to LC-MS Metabolomics
E23-30: ABC to PMP: A Project Management Crash Course
E23: Problems with FT-IR Spectra and How to Avoid Them, provided in collaboration with SAS
E23: Intact and Top-Down Protein Characterization and Quantitation by Mass Spectrometry: Approaches for Pharmaceutical Drug Discovery, Development, and Bioanalysis
E23: Sample Preparation: The Chemistry Behind the Techniques
E24-01: Interpretation of Infrared and Raman Spectra
E24-02: High-Performance Thin-Layer Chromatography a Reliable Analytical Technique in a Quality Control Environment.
E24-05: A Holistic Approach to Life Cycle Management of Nitrosamine Drug Substance Related Impurity in Pharmaceutical Products: Guidance and Case Study
E24-07: Establish a Quality System to Maintain Data Integrity in the Pharmaceutical Labs
E24-10: Applications of Portable Spectroscopy in Pharma, Forensics and Law Enforcement
E24-27: HPLC Operating Modes Primer: Reversed-Phase and Other Options
E25: Bioanalytical Method Validation by LC-MS/MS
E25: Chromatographic Methods of Analysis of Oligonucleotides, siRNA, and mRNA
E25: Collecting Infrared Spectra and Avoiding the Pitfalls
E25: Practical NMR Spectroscopy
E25: Successfully Implementing Key Elements of the USP and ICH Guidances in an Enhanced Analytical Procedure Development Workflow
E25: Advanced Chemometrics without Equations (or Hardly Any)
E25: An Overview of Drug Development, Drug Quality, Regulatory, and Quality Control Processes
E25: Analytical Target Profile: An Introduction and its Strategic Link to Quality Target Product Profile and Analytical Life Cycle Management
E25: Data Analysis Skills for Chromatographers
E25: Getting the Most from GC and GC/MS
E25: How to Deliver a Winning Technical Presentation
E25: HPLC and UHPLC for Practicing Scientists 1 and 2: Fundamentals, Method Development, and Troubleshooting
E25: Introduction to Data Analytics for Analytical Chemists
E25: Introduction to Quantitative Spectroscopy for Quality Assurance in the R&D and Manufacturing Environments
E25: LA-ICP-MS: Theory, Practice, and Environmental and Biological Applications
E25: Practical LC-MS/MS Method Development and Sample Preparation
E25: Process Analytical Technology: Out of the Lab and into the Line
E25: Real-Time Insights into Electrochemical Reactions: Operando/In-Situ Raman and Optical Imaging
E25: Supercritical Fluid Chromatography (SFC): A Powerful and Greener Tool for Analytical and Preparative Separations
E25: Systematic HPLC Troubleshooting
E25: The Fundamentals of Laboratory Management – Managing People
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