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 * E20: Machine Learning for Chemometricians: ANNs, SVMs, XGBoost and other
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 * E20: Modern Size Exclusion Chromatography of Synthetic Polymers and
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 * 2015
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 * April Retort
 * Booth Application 2021
 * Call for Award Nominations, Young Investigator & Student Awards
 * Call for Paper Submission Details
 * Call for Papers
 * Call for Papers – Deadline Extended until April 30th
 * Call for Student Representative
 * Conferences-in-Miniature
 * Conferences-In-Miniature
 * Contact Us
 * Digital Advertising Opportunities
 * Driving Directions
 * 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
 * E21-13: Effective Communication for Multicultural Professionals
 * 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: HPTLC – The Other High-Performance Chromatography: Parameters,
   Applications, Method Development and Troubleshooting
 * E22-04: Chemometrics without Equations Parts 1 & 2
 * E22-11: Portable Spectroscopy and Its Application in Forensic Science
 * 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
 * E22-22: Analytical Atomic Spectroscopy and its Environmental Applications
 * 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
 * E22: Introduction to Chemometrics without Equations (Part 1)
 * E23-01: HPLC and UHPLC for Practicing Scientists 1 and 2: Fundamentals,
   Method Development, and Troubleshooting
 * E23-02 HPLC and UHPLC for Practicing Scientists Part 1 ONLY: Fundamentals
 * E23-02: HPLC & UHPLC for Practicing Scientists Part 1: Fundamentals
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   Quality: Standardization, Quantification and Automation
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