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Pharmaceutical QA/QC Investigations Webinars
Here you can replay our collection of webinars on pharmaceutical QA/QC investigation topics. These webinars cover a broad range of analytical topics relating to the investigation of drug product manufacturing issues including topics such as particle contamination, raw materials analysis, glass delamination and product failure.
By Tifanie Tiberio on November 18, 2015
During this webinar we will discuss the variety of methods that have been investigated in an attempt to identify an automated protocol for the specific (chemical and/or morphological) counting and sizing of glass lamellae in parenteral drug solutions.
By Admin on July 1, 2015
During this webinar, Gateway Analytical scientists will present an overview of manual (SEM-EDS, microscopy, FTIR, and Raman) and automated (automated SEM, CCSEM) methodologies for characterizing foreign particulate matter in pharmaceutical investigations and cleanliness studies. Several case study examples will be presented showing the various approaches to particulate identification and the utility of both types of analyses.
Posted in Material Science Replays, Pharmaceutical QA/QC Investigations Webinars, Pharmaceutical Webinars, Recorded Webinars | Tagged characterizing foreign particulate, cleanliness studies, Foreign Particulate Analysis, FTIR spectroscopy, pharmaceutical investigations, quality control testing, SEM | Leave a response
By Admin on July 1, 2015
During this webinar we will discuss Raman and LIBS technology and the Rap-ID SPE-Is raman.ID + Metal.ID system as a tool for providing automated particle sizing and characterization. In addition, we will also discuss some of the most commonly found sources of foreign particulate and present application and case study examples of automated particle identification.
Posted in Pharmaceutical QA/QC Investigations Webinars, Pharmaceutical Webinars, Recorded Webinars | Tagged automated particle sizing, foreign particulate, LIBS, particle characterization, Raman | Leave a response
By Admin on March 26, 2014
Join David Exline, Vice President of Gateway Analytical and Dr. Oliver K. Valet, Co-founder of rap-ID Particle Systems as they share their combined 30 years of experience providing particle identification services to pharmaceutical drug manufactures in need. During this webinar they will discuss Raman and LIBS technology and the rap-ID SPE-Is raman.ID + Metal.ID system that they use to provide automated particle sizing and characterization. In addition, they will also discuss some of the most commonly found sources of foreign particulate and present application and case study examples of automated particle identification.
Posted in Pharmaceutical QA/QC Investigations Webinars, Pharmaceutical Webinars, Recorded Webinars | Tagged automated particle characterization, automated particle identification, automated particle sizing, LIBS, particle identification, Raman spectroscopy | 3 Responses
By Admin on February 4, 2014
Glass delamination can be a costly problem for pharmaceutical drug vial manufactures. For one vial manufacturer glass delamination can cause the recall of thousands of vials of drug product. In this webinar, you will learn about the common types of problems caused by glass delamination in pharmaceutical vials and the analytical testing processes Gateway Analytical uses to evaluate them.