Recorded Webinars

Curiosity + Expertise = Innovation.

Complex technical concepts can often obscure the path to understanding. At Gateway Analytical, we believe in demystifying these intricacies. That’s why our team of expert scientists has embarked on a mission to break down the barriers of scientific jargon.

Our recorded webinars are designed to provide clarity and insight into the fascinating world of analytical science. We take these complex technical concepts and present them in a way that everyone can grasp. Join us in unraveling the mysteries, one webinar at a time.

Ensuring Container Integrity at Various Temperatures

In the fast-paced world of pharmaceutical development and manufacturing, ensuring the integrity of sterile containers is paramount. This webinar, titled “Ensuring Container Integrity at Various

The Value of Presumptive Screening of Physical Evidence

Authors & ContributorsDavid ExlineCara Plese May 06, 2013 Presumptive tests for blood, seminal fluid, urine, and saliva are fast, relatively inexpensive, and can quickly eliminate a stain from further analysis if the results show the sample is not the fluid originally suspected. Likewise, microscopic analysis of hair is a nondestructive…

Case Studies in Foreign Particulate Analysis

Topics covered include analytical techniques and methods suitable for API particle sizing and in vitro bioequivalence for nasal drug products as well as preparation methods

Controlled Release Testing Using Raman Chemical Imaging

May 14, 2012 When developing controlled release products, it is important to establish coating consistencies in the laboratory and manufacturing environments to produce a predictable result.  The ability to effectively test and gain feedback about the coating processes for ingredient-specific measurements of individual coating layers, allows scientists to accurately predict…

In Depth Analysis of Particle Contamination for Tablet and Semi-Solid Drug Products

Authors & ContributorsDavid ExlineCara PleseAugust 28, 2013 This webinar was designed for professionals (e.g. Quality Control, Industrial Engineers) involved in the production and development of tablet and semi-solid drug products. During this webinar, our presenters provided examples of commonly found  particle contamination in tablet and semi-solid drug products and how these…

What Police and Attorneys Need to Know about Gunshot Residue Analysis

Authors & ContributorsRebekah ByrneDavid Exline January 02, 2013 This webinar was designed for police and attorneys and built upon the information provided in our previous webinar, “Forensic Analysis of Gunshot Residue for Police & Attorneys.”  During this webinar, our presenters provided police officers with tips on the proper collection for…

Forensic Analysis of Condom Lubricants for Police & Attorneys

Authors & ContributorsCara PleseAntonio Scatena May 17, 2012 This webinar covers the collection, documentation, and forensic analysis  of condom lubricants and sexual assault evidence. Scientific principles and current methods of condom lubricant analysis are covered to help investigators review and present in casework. Case studies related to the use of condom…

Forensic Analysis of Paint and Tapes for Police & Attorneys

Authors & ContributorsDavid Exline May 13, 2012 This webinar covers the forensic investigation process for paint and tape evidence. Topics include the most current methods used for today’s investigators and discuss the interpretation of paint transfer evidence. Case studies related to the analysis of duct tapes, automotive and architectural paints…

Early-Phase Development

Comprehensive packages designed to navigate clinical & regulatory complexities of parenteral product-package and container-closure development, from concept to market readiness.

Container Closure
Integrity Testing

Quantitative, non-destructive, deterministic leak detection technologies for products stored in vials, syringes, cartridges, flexible containers, and bottles.

Particulate
Analysis

Multi-analytical methods to count, size, and characterize visible and subvisible particulate matter in pharmaceuticals, disposable containers, single-use systems, raw materials, and medical devices.

Medical Device
Analysis

Rigorous studies focused on enumerating particulate matter and identifying potential chemical compounds that could migrate from medical devices into the environment or directly impact patient health.

Extractables
& Leachables

Studies aimed at identifying potentially harmful compounds in manufacturing components and final containers to ensure the safety and efficacy of pharmaceutical products.

Empowering Your Journey Toward Enhanced Patient Care

Covering every stage of the drug development journey with our state-of-the-art, FDA-inspected, cGMP-compliant facilities designed to minimize bottlenecks and maximize success.