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Thermo Fisher Scientific
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HPLC Method Transfer: A CDMO perspective

ZÁZNAM | Proběhlo Čt, 19.5.2022
Budeme sdílet klíčové poznatky, zpětnou vazbu a osvědčené postupy pro přenos metod z konkurenčních HPLC a vývoj nových na HPLC platformu Vanquish.
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Thermo Scientific: HPLC Method Transfer: A CDMO perspective

Thermo Scientific: HPLC Method Transfer: A CDMO perspective

In this webinar, two Analytical Development Lab Chemists will share key learnings, feedback and best practices for transferring methods from competitive instruments and developing new ones onto the Vanquish liquid chromatography platform. The xriteria for the chosen technology was strict:

  • Compatible with existing IT infrastructure (Waters™ Empower™ 3 Chromatography Data Software)
  • Suitable for the analysis of both chemical and biologic molecules
  • Both HPLC and UHPLC performance for compatibility with legacy HPLC methods as well as more modern UHPLC assays
  • Seamless method transfer capabilities

Key Learning Objectives:

  • (U)HPLC method transfer cross platforms
  • Integration of Thermo Scientific Vanquish platforms into an existing Waters™ Empower™ 3 environment
  • Overcoming hesitancy of change

Who Should Attend:

  • Laboratory managers
  • CDMO, CRO and Pharma scientists
  • Department / business heads and principle scientists

Presenter: Nolan Dean (Staff R&D Mfg Scientist, Thermo Fisher Scientific)

Nolan has been working in the pharmaceutical industry for the past 14 years as an analytical development scientist. He worked in CDMOs and Large Pharma GMP Manufacturing focusing on analytical method development and validation as well as quality control testing. He joined the Greenville, NC Thermo Fisher Scientific Pharma Service Group location in 2017 as a member of the analytical development group.

Presenter: Blake Bailey (Supervisor R&D Mfg Scientist, Thermo Fisher Scientific)

Blake has been working in the pharmaceutical industry for the past 12 years as an analytical chemist and as a R&D supervisor. He worked in CDMOs and Large Pharma GMP Manufacturing focusing on analytical method development and validation as well as quality control testing. He joined the Greenville, NC Thermo Fisher Scientific Pharma Service Group location in 2016 following the acquisition of Patheon, which he worked for since 2012.

Thermo Fisher Scientific
 

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