Manufacturing and Analytical Characterization - Chemical

(T0930-02-08) API – Polymer Interactions with Dissolution Media: A Key Consideration in Method Development for Amorphous Solid Dispersions

(M0930-02-08) Impact of Excipient Properties on Coning during Dissolution for Ibuprofen Formulations

(W0930-02-08) Optimization of UV Detector Parameters of Compendial Methods

(M0930-02-09) Revealing the Stable δ²H, δ¹³C, and δ¹⁸O Isotopic Patterns of Ibuprofen Drug Products and Commonly used Pharmaceutical Excipients

(W0930-02-10) Enabling Advanced Manufacturing Technologies and Quality by Control (QbC) with the Implementation of Advanced Process Control

(T0930-02-11) Enhancing Environmental Sustainability in the Korean Pharmacopoeia: Replacement of Carbon Tetrachloride in the Monograph for Epinephrine Injection

(W0930-02-11) Impact of Direct Vs Indirect Simulation on Material Strength and Deformation Parameters

(W0930-02-12) A High Throughput In Vitro Screening Method for Cocrystal Food Effect Evaluation

(M0930-02-12) CFD-DEM Modeling of Floating Particle Mixing in Pharmaceutical Manufacturing

(T0930-02-12) Real-Time Monitoring of Selective Laser Sintering 3D Printing Process For Lamivudine Content Quantification in the Printlets

(W0930-02-13) Continuous Manufacturing of Injectable Nanoemulsions: Methods and Characterization

(T0930-02-13) Influence of Temperature, Vacuum, and Humidity on Drying Kinetics of Citric Acid Monohydrate

(M0930-02-14) Development of Powdered SERS Tags for Direct Compression: Toward On-Dose Authentication for Anti-Counterfeiting and Medication Management

(W0930-02-14) HPLC Method Development for Assay of Common Topical Formulation Preservatives

(T0930-02-14) Quantitative Structural and Compositional Elucidation of Real‑World Pharmaceutical Tablet Using Large Field‑of‑View, Correlative Microscopy‑Tomography Techniques and AI‑Enabled Image Analysis

(M1030-02-08) Evaluation of Tableting Characteristics of Copovidone-Based ASDs Using CTC and Heckle Analysis

(W1030-02-08) Raman Spectroscopy as a PAT Tool for Hot Melt Extrusion

(T1030-02-08) Rethinking In Vitro Testing: Using Biorelevant Media for Dispersion/Dissolution Testing for Lipid-Based Drug Delivery

(W1030-02-10) Detection of Xanthines and Several Beta-Lactam Antibiotics Using Surface Modified Lipid/Polymer Membranes

(M1030-02-10) Drugs in Space: Evaluating the Effects of Drug-Product Package Changes in Drug Stability

(W1030-02-11) Ethanol Vapour-Induced Morphological Influences on the Water Barrier Performance of PLA Packaging: A Multi-Component Study

(M1030-02-11) Nitrite Detection at Trace Levels: Insights from a Lactose Case Study on Ion Chromatography and Sonication Effects

(T1030-02-12) Consistent Dry-Coating Process for Preparing Functional Particles with Novel Coating Using Two-Step Melt Granulation

(W1030-02-12) Crystal Defects Cause Nitrosamine Formation in Ranitidine under Accelerate Storage Condition

(M1030-02-12) Decoding Choice of Surrogate Compounds for TSMG Empirical Modelling of Gabapentin - A Case Study

(T1030-02-13) Investigating Granule Temperature Dynamics and Its Impact on Granule Properties during Long TSMG Runs

(T1030-02-14) Quality Demonstration of Personalized Mini Tablet Manufacture Using Integrated Single-Dose Manufacturing System

(W1130-02-08) Room-Temperature Aerosol Dehydration Enables Production of Stable Bevacizumab Powder from FDA-Approved Avastin®

(M1130-02-09) Powder Rheology for Batch Comparison During Manufacturing

(W1130-02-10) Defining a Robust, Discovery-Scale Process to Manufacture PLGA Microsphere Prototypes

(T1130-02-10) The Use of Raman Mapping and Hot-Stage Microscopy to Detect Micro-Domains of Crystallinity in Amorphous Solid Dispersions of Nilotinib

(M1130-02-10) Understanding How UHPLC System Characteristics Effect “Going Green” with Regulated Methods

(W1130-02-11) Adapting USP Monographs to the Capillary Scale using USP 621

(T1130-02-11) Impact of Material Spring Behavior on the Sticking Propensity During Tablet Manufacturing: Part 1- Single Component Pharmaceutical Systems

(M1130-02-12) Establishing the Mechanism of Immediate Release Film Coating Dissolution Using Terahertz Measurements

(W1130-02-12) Sustainable Separation: Supercritical Fluid Chromatography as a Modern Replacement for Normal Phase Chromatography

(T1130-02-12) Why Rheology Matters: Insights into Granulation Behavior in Twin-Screw Melt Granulation

(T1130-02-13) Microscope-Enabled Disc Dissolution System: Concordance between Drug and Polymer Dissolution from an Amorphous Solid Dispersion Disc and Visual Disc Degradation

(W1130-02-13) Multi-Compartment In Vitro Dissolution Testing to Study the Potential Impact of API Changes on Drug-in-Capsule Absorption for Mobocertinib, a Weak Base with Complex pH-Dependent Solubility

(W1130-02-14) Contactless, Real-Time Thermal Profiling and Control of Exothermic and Endothermic Reactions

(M1130-02-14) Enabling Inline Concentration Control: Refractometry as a PAT Tool in Continuous Manufacturing of Lipid-Based Therapeutics

(T1130-02-14) Low Viscosity Hypromellose for Capsule Banding and Tablet Coating Applications via Ethanol (Isopropanol)/Water Solvent Media

(M1230-02-08) Discrete Element Method (DEM) Study of a Batch Blending Process

(T1230-02-08) UPLC Investigation for Understanding Excipient Interactions to Enhance Stability in a Transdermal Apixaban Delivery System

(T1230-02-09) Establishing Linear Viscoelastic Region and Gelation Dynamics in Anhydrous Intra Nasal Gel: Rheological Insights toward Optimized Patient-Centric Formulations

(T1230-02-10) Unraveling the Bridging Region of Lenacapavir Atropisomers by 2D-LC

(T1230-02-11) Engineering and Formulation Space Optimization of pH-Sensitive Granules for Delayed Drug Release by Twin Screw Melt Granulation

(M1230-02-11) Synergistic Integration of Twin-Screw Hot-Melt Granulation and Selective Laser Melting for High-Dose Extended-Release 3D-Printed Tablets

(M1230-02-12) Improving Stability and Sustainability of an Auto-Oxidative Excipient, Polyethylene Oxide, with Foil-Lined Packaging

(T1230-02-12) Producing ASDs with Pressure Nozzles Using Laboratory Scale Spray Dryers

(M1230-02-13) Mechanistic Understanding of Sodium Metabisulfite-Induced Drug Degradation: An Interplay of In Silico and Experimental Studies

(T1230-02-13) Spray Dry Granulation in Fluid Bed Technology and Scale Up

(M1230-02-14) Optimization of Roller Compaction Process for Highly Unstable Drug Substance Susceptible to Degradation in Presence of Moisture, Oxygen and Magnesium Stearate

(M1330-02-08) Chromatographic Method for Determination of 6-mercaptopurine in Skin Permeation Assays

(T1330-02-08) Super-Fast Fabrication of Drug Nanocrystals Using Dual Asymmetric Centrifugation: An Efficient Approach for High-Throughput Formulation Screening

(T1330-02-10) Development of a SMEDDS-Based Tablet for Sustained Release and Improved Solubility of Apixaban

(M1330-02-11) Aseptic Spray Drying and Homogenization for the Manufacture of a Sterile Long-Acting Injectable (LAI) Formulation

(T1330-02-11) Impact of In-Die Compression Behavior on the Sticking Propensity During Tablet Manufacturing: Binary Component Pharmaceutical Systems

(T1330-02-13) Role of Surface Morphological Characteristics of Substrate in Adhesion Performance of Topical and Transdermal Delivery Systems (TDS)

(M1330-02-13) Scalable Agile 3D Material Inkjet Printing and Analysis of Oral Pharmaceuticals – A Case Study for Digitally Prescribed Dose and In-Line Dose Verification

(T1430-02-08) LC-MS Workflow for Rapid and Precise Impurity Profiling of Oligonucleotides and GLP-1a

(M1430-02-08) Quantitating Swelling Pressure Generated by the Push Layer of an Osmotic Pump Tablet

(M1430-02-09) Advancing Lean Chemometrics: Minimizing Material Expenditure with Iterative Optimization Technology

(T1430-02-09) Cracking the Chromatographic Code: Innovative Solutions to Address Keto-Enol Tautomerism in LC Method Development

(T1430-02-10) Development of a Modified Arrhenius Equation to Predict the Kinetics of N-nitrosation of Active Drug in Solid Dosage Form

(M1430-02-11) Fast and Efficient Development of a DC Formulation of Ondansetron Tablets Guided by a Digital Tool

(T1430-02-11) Monitoring of NO_X Concentration on Fluidized Bed Dryer and Evaluation of Its Reduction Method

(M1430-02-12) Development of Combination Printlets of Sulfadiazine and Pyrimethamine Using Selective Laser Sintering 3D Printing for Pediatrics Applications

(T1430-02-12) Highly Controlled Drug Nanoparticles Generation by Vapor Jet De-sublimation

(M1430-02-13) Diethylene Glycol and Ethylene Glycol Challenges: Compendial Approach and Emerging Standards

(T1430-02-13) Evaluation of Compaction Properties of Several Hydrophilic Polymers and Tableting Components in the Development of a Prototype Directly Compressible Gastroretentive Extended-Release Tablet

(T1430-02-14) Risk-Based Computer System Validation in Pharmaceutical Quality Systems: Practical Outcomes from an Analytical Laboratory Implementation

(M1530-02-08) Compression Process Optimization Using a 2^3 Full Factorial Design of Experiments

(T1530-02-10) Spray Drying of Low Organic Solubility Pharmaceutical Compounds, a Vemurafenib Case Study

(T1530-02-11) Analysis of Lubrication Process Impact on Formulation Blend and Tableting Properties with Numerical Models and Statistical Analysis

(M1530-02-11) Die Modeling for Extruded Implants

(T1530-02-12) Development of Spray Freeze Drying as a Novel Strategy to Enhance the Oral Delivery of Proteins/Peptides

(M1530-02-12) Powder-Discharge KinetiSol® Process Produces Nano- and Micron-Sized Particle Aggregates for Drug Delivery

(T1530-02-13) De-Risking Tablet Formulation Development Using Compaction Simulation

(M1530-02-14) Functional Evaluation of Disintegrants Mixed into Pharmaceutical Excipients Based on Dynamic Viscoelastic Measurements

(T1530-02-14) Scaling-Up from the Bench: Model Based Approaches to Dry Granulation