Webinars are a great way to learn about the latest pharmaceutical tools and technologies from the most trusted thought leaders in the industry. American Pharmaceutical Review produces numerous webinars covering a wide variety of topics of importance to the industry. Here you will find all of the webinars we have produced. This is a great resource, and one you can access on-demand to fit your schedule.
Thursday, December 09, 2021
In this webinar we will discuss how recent technological developments allow for rapid micro testing and rapid micro identification, focusing on the genotypic identification method and equipment that ...
Thursday, November 04, 2021
In this webinar you’ll learn: Identification of unknown particles in a wide variety of manufacturing processes. Reverse engineering and failure analysis in the manufacturing process. Two-step ...
Thursday, October 28, 2021
This webinar will provide a review of validation strategies and implementation for a rapid at-line mycoplasma test for cell therapy companies.
Tuesday, October 26, 2021
In this webinar you’ll learn answers to common questions to distinguish actual pharmacopeial requirements for pharmaceutical waters vs what has become widely accepted in the industry and thought to be...
Tuesday, October 05, 2021
This webinar will share Ionis’ experience with developing and validating a platform SoloVPE® in-process assay method for GMP manufacturing of oligonucleotide drug products. It will describe how to ...
Wednesday, September 01, 2021
This webinar will provide scientists and technical stakeholders working in drug delivery with a detailed explanation of theory and application of an exciting extended-release technology platform for ...
Thursday, August 26, 2021
On-Demand Webinar: A Straightforward Path Toward Regulatory Compliance and Data Integrity with Your Microbial Testing Systems
Live Webinar: Increase Overall GMP Operational Efficiencies with Dilution-free Concentration Measurement and Capital ROI within 12 Months
In this webinar, you’ll learn the essentials of Growth Promotion Testing, why Environmental Monitoring should be a part of your QC program, and a year in review of using BCC for USP <60>.60>
Webinar: How Vibrational Spectroscopy Helps to Accelerate New Drug Development and to Troubleshoot Drug Production
Live Webinar: "A Little Too Quiet” – Case Study on Asset Utilization
In this webinar, you’ll learn about the additional challenges COVID presented to already compressed timelines and the strategies AES utilized to rapidly mobilize and meet the country’s needs, the ...
In this webinar you’ll learn: optimizing final formulation of drug products with albumin; how to avoid the variable nature of albumin’s structure, how it affects function, and how purity solves these ...
This webinar will address how to deal with “Risk Assessment for Potential Elemental Impurities” on Drug Products and Medical Devices. The USP, in parallel with the International Council for ...
In this webinar you’ll learn: overview of current regulatory requirements for residual DNA clearance for biological products including residual plasmid DNA and how this applies to gene therapy and ...