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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
- E21-13: 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: 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: Portable Spectroscopy and Its Application in Forensic Science
- 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
- E22-22: Analytical Atomic Spectroscopy and its Environmental Applications
- E22-24: Problems with FT-IR Spectra and How to Avoid Them, provided in collaboration with SAS
- 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
- E23-03: Sample Preparation: The Chemistry Behind the Techniques
- E23-05: Practical NMR Spectroscopy
- E23-07: High-Performance Thin-Layer Chromatography an Alternative Approach to Quality: Standardization, Quantification and Automation
- E23-08: Practical LC-MS Method Development and Sample Preparation
- E23-09: Non-Linear Machine Learning for Calibration and Classification
- E23-11: Prepare Your Analytical Laboratory for Quality Audit and Inspection
- E23-12: Green Analytical Chemistry
- E23-13: HPLC and UHPLC for Practicing Scientists Part 2 ONLY: Applications, UHPLC, Method Development, and Troubleshooting
- E23-14: Introduction to Quantitative Spectroscopy for Near Infrared and Raman Instrumentation
- 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
- E23-28: An Overview of Drug Development, Drug Quality, Regulatory, and Quality Control Processes
- E23-29: Systematic Chromatography Maintenance and Troubleshooting
- E23-30: ABC to PMP: A Project Management Crash Course
- E23: Introduction to Infrared, Raman and Near Infrared Spectroscopy
- E23: Practical Bioanalytical Method Validation by LC-MS/MS
- 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: Process Analytical Technology: Out of the Lab and into the Line
- E23: Sample Preparation: The Chemistry Behind the Techniques
- E23: Systematic Chromatography Maintenance and Troubleshooting
- E24: Chromatographic Methods of Analysis of Oligonucleotides, siRNA, sgRNA and mRNA
- E24: Getting the Most from GC and GC/MS
- E24: Practical LC-MS Method Development and Sample Preparation
- E24: Supercritical Fluid Chromatography (SFC): A Powerful and Greener Tool for Analytical and Preparative Separations
- E240: The Fundamentals of Laboratory Management – Managing People
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