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Here you can replay our collection of webinars on pharmaceutical topics. Our pharmaceutical webinars cover a broad range of analytical topics relating to the drug delivery and development of generic and innovator drugs. Our speakers go into great detail about the analytical techniques and technology they use to do analysis such as ingredient-specific particle sizing, controlled release testing, polymorph analysis, evaluating content uniformity and more.
By Admin on October 5, 2016
When: October 27, 2016 Time: 2PM (ET, US & Canada) Presenters: David Exline, President, Gateway Analytical, and Julie D. Suman, Ph.D., President, Next Breath, LLC Overview 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 drug […]
By Admin on July 1, 2016
When: July 27, 2016 Time: 2PM Presenter: Cara Plese, Scientist Overview Foreign particulate in drug products originate from a variety of sources. Such sources can include machinery used in drug manufacturing, drug packaging components, cleaning utensils and products, personnel wearing personal protective equipment (PPE) and laboratory surfaces. Typical contaminants include polymers, fibers, burnt material and […]
By Tifanie Tiberio on October 15, 2015
Next Breath and Gateway Analytical have partnered to present insight into an OINDP Webinar Series for Dry Powder Inhalers (DPIs), pressurized Metered Dose Inhaler (MDIs), and Nasal drug products. These complex delivery systems and their development require key specialized expertise and during this webinar we will provide a comprehensive review of their in-house analytical technologies, GMP methods, and specialized expertise. To insure adequate time and focus, Next Breath and Gateway Analytical will structure the webinar in four series. Webinar 1 scheduled on October 14th will focus on Nasal Sprays Drug Product Development.
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