Category: On Demand and Past Events

Keeping Pace with COVID-19 Virtual Symposium

COVID-19 research and testing methods are evolving every day. Join us for an interactive live event to hear the latest on what leading researchers and labs are doing to keep pace.
You will discover best practices for applying technology to support COVID-19 research, test development, and vaccine and drug development – and how these workflows can be effectively applied toward other infectious diseases as well.

 

Register to access a diverse lineup of speakers and sessions, including:

  • Collaborating in the fight against COVID-19
  • A next-generation tool bench for virology research
  • Keynote presentation: Viral hijacking of cellular metabolism
  • Seahorse XF reveals bioenergetic impact in virology
  • Rapid functional evaluation of virus-neutralizing antibodies and antiviral drugs using multiparametric live-cell analysis
  • Focus on virology: Applications to enable discovery
  • SLIMS: Easier and faster LIMS deployment for COVID
  • Faster in, faster out: Achieve the most efficient analysis of raw material for vaccine production
  • Agilent BioMDS solutions for vaccine research
  • Agilent GC solution for alcohol-based hand sanitizer testing
  • Analysis of alcohol levels in hand sanitizer formulations using Cary 630 FTIR
  • QA/QC of protection masks

 

Agenda

 

Register Here >

 

A New Endotoxin Testing Platform: Sievers Eclipse BET

In this webinar, attendees will receive an introduction to the groundbreaking Sievers Eclipse BET Platform to understand why it was created and how it works to simplify and automate endotoxin assay setup, while maintaining full compliance with USP <85>. With Eclipse, compliant 21-sample assays can be set up in as little as 9 minutes, leading to substantial efficiency gains.

This webinar will also focus on how to evaluate this revolutionary technology. From comparability of analytical results across platforms to data integrity and validation testing, this webinar will leave attendees with a solid understanding of how the Eclipse platform stacks up next to other technology on the market, and how it can be evaluated and validated in a QC lab to demonstrate viability for routine endotoxin testing.

 

In this webinar you’ll learn:

  • Why and how the Sievers Eclipse platform was developed
  • How the Eclipse platform increases efficiency and automates endotoxin testing
  • How the Eclipse platform aligns with USP <85>, EP 2.6.14, and JP 4.01
  • Comparability of analytical results across different platforms
  • Data integrity
  • Validation testing and validation tools available to customers

 

Who should attend:

  • QA & QC personnel
  • Microbiology personnel
  • Validation personnel
  • Metrology personnel
  • Operations personnel

 

 Register Here >

 

TOC and Conductivity Analysis: Back to Basics

This webinar is designed to get back to basics as a refresher for seasoned users or as an introduction for those new to total organic carbon (TOC) and conductivity analysis, USP <643>, and USP <645>.

Join this interactive discussion to learn practical tips for day-to-day use of TOC for compendial water testing and cleaning validation.Total organic carbon (TOC) and conductivity analysis can be used in a variety of applications and are very useful in assessing cleanliness, water quality, and process performance.

It is compulsory for manufactures to abide by the regulations for TOC and conductivity, however, not all end users understand how the technology works and why it is important. In this webinar we’ll cover the basics and provide quick tips for success from the user’s perspective.

 

This webinar will cover:

  • Regulations: Understanding USP <643> Total Organic Carbon, USP <645> Conductivity, data integrity, and regulatory expectations for cleaning validation
  • Basic principles of TOC and conductivity: Overview of Sievers technology and applications
  • Data analysis: What story are the data telling?
  • Best practices, troubleshooting, and quick tips
  • Data integrity and validation

 

Who should attend:

  • QA & QC personnel
  • Validation personnel
  • Operations personnel

 

 Register Here >