What is Pharmaceutical Forensics?
Watch Gateway Analytical's Dave Exline discuss our pharmaceutical forensics services.
Comparison of Raman and FTIR Spectroscopy: Advantages and Limitations
Authors & Contributors David Exline October 09, 2013
2018 RDD Conference: Analysis of a Dry Powder Inhaler Active Pharmaceutical Ingredient Using Scanning Electron Microscopy
Download our presentation from 2018 RDD Conference on Analysis of a Dry Powder Inhaler Active Pharmaceutical Ingredient Using Scanning Electron Microscopy.
Wear Debris Characterization using Automated Raman and SEM-EDS
Authors & ContributorsRebekah ByrneDavid ExlineSeptember 17, 2015
Gateway Analytical Presents on Analytical Testing Methods for Inhalable Drug Products at Medicon Valley Inhalation Symposium
Gateway Analytical announces participation in the 6th Medicon Valley Inhalation Symposium (MVIS) in Lund, Sweden being held on October 11-12, 2017. Gateway Analytical will serve as one of the platinum…
Chemically Specific API Particle Sizing Using Automated Raman Spectroscopy
The active pharmaceutical ingredient (API) size distribution within the final formulation of a drug product is critical as it relates to bioavailability, rates of absorption, and stability of that…
Gateway Analytical to Present Latest Methodologies for Glass Delamination Analysis at Annual Meeting of Pharmaceutical Scientists
Gateway Analytical announced today that they will give a scientific poster presentation on glass delamination analysis in addition to exhibiting at the upcoming 2015 American Association of Pharmaceutical Scientists (AAPS)…
DDL 2014: Chemically-specific Characterization of Particulate in Inhalable Drug Products using Raman and Laser-induced Breakdown Spectroscopy
December 11, 2014 The impact of foreign particulate and agglomerates on dissolution profile and permeability of the inhalable drug particles within the sites of action (i.e. patient’s lungs) is critical. In this study, Raman Chemical Imaging (RCI) and Raman/ Laser-induced breakdown spectroscopy (LIBS) were used to investigate the Active Pharmaceutical…
A Dual Automated Approach for Sizing and Characterizing Budesonide In Suspension Utilizing Automated Raman and Automated SEM-EDS
Part of USDA requirements for in vitro bioequivalence testing is particle size distribution and agglomerate analysis of the budesonide suspension in the ampoules of both the generic product for submission…
Structuring Your Materials Characterization with Raman Spectroscopy
Download our webinar on structuring your materials characterization with raman spectroscopy.