Click to join or renew
ISPE Logo - Click to go to the ISPE home page

eLearning


Search

for

Log in
Name: Development and Validation of a fully automated device for sterile connection of large and liquid filled TPE tubing ( WEB111201 )
Description: Online Registration is now closed - please call member services at Tel: +1-813-960-2105, Fax: +1-813-264-2816

Live Webinar: 1 December, 11:00 – 11:45 AM EST

This presentation will first introduce the traditional operating procedures to perform sterile connection mostly used in the past (connections under laminar flow, autoclave), and will then give an overview of the new innovating technologies available on the market for sterile connection according to tubing properties.

Objectives:
The session objective is first to position the innovating technology regarding the solutions available on the market, and then walk the end-user through the full automated device, the applications, how it works and validation tests. The fully automated device allows fast and reliable sterile connection of large and liquid filled thermoplastic tubing in biopharmaceutical applications, which increases operation effectiveness and efficiency.

At the conclusion of this session, participants will be able to:
  • Understand how the automated device works, the applications, and the various validation tests.
  • Understand the technologies available and how to define the best solution according to the application for your organization.

  • Who should attend - (job types / titles):

    Validation engineers & managers, Production engineers & managers, Technical engineers & managers, R&D engineers & managers, Product manager, purchasing managers

    Presenter Biography:

    Myriam Bengaoui, Global Program Manager Associate, Sartorius Stedim Biotech, Aubagne, France.

    Her product portfolio includes sterile connectors, welding and sealing equipments and single-use transfer sets. She has 5 years of experience in engineering and marketing in the Biopharmaceutical industries and has been involved in many industrial projects for design, implementation and validation of single-use systems.

    Myriam started her career in 2005 as a Process Engineer with GlaxoSmithKline Biologicals, Belgium. In 2007, she joined Sartorius Stedim Biotech as a Process Development Engineer for Fluid Management Technologies.

    Myriam is a Process Engineer graduated from the “Ecole des Mines” of Albi, France.
    URL:
    CEUs: .075
    Member Price: US Dollar        EURO
    Non Member Price: US Dollar        EURO
    Instructors:
    Copyright 1997- International Society for Pharmaceutical Engineering   |   Privacy Policy   |   Terms of Use