57% say moving single use systems from development into commercial production is their main goal for 2012…

...biomanufacturing and single use are becoming synonymous. Single use found fame in R&D and is now working its way through to clinical manufacturing with a view to dominating commercial manufacturing scales. However, efficiency savings still need to be maintained.

This has brought new challenges;

  • Choosing the right equipment
  • Closing the gap between upstream and downstream technology
  • Disposal and sustainable waste management

How are you overcoming these obstacles?

The Disposable Solutions for Biomanufacturing event has been developed along with our expert advisory board in order to address the issues that matter most to you.

The conference is the most interactive yet, in order to provide you with the best possible platform to discuss the strategic and regulatory challenges of biomanufacturing and find out how others are tackling these. It’s the perfect chance to network, with your peers, meet new suppliers and forge new contacts.

The event will be taking place on the 28th-29th February 2012 – take advantage of our early bird discount and register now so you don’t miss out!

What’s New for 2012?

  • Technology demonstrations – we’re bringing you the latest upstream and downstream product launches all under one roof!
  • Focus on scale up to clinical trial material and market level manufacturing with 2 exclusive case studies as to how this can be achieved
  • A look into the new ICH q9 guidelines, how can QbD improve your efficiency?
  • The impact of single use technology on stem cell bioprocessing with Stephen Brown
  • More interactivity than ever before – discussion sessions from last year are back by popular demand and much more!
  • All day site visit to Novasep’s Gosselies and Seneffe facilities
  • Online preconference learning with a series of webinars

Download the agenda for all the details…

If you didn’t make it last year, here is what our 2011 attendees thought…

"Very valuable" - MSD Biologics UK
"Excellent mix of speakers & topics. Very valuable." - Pfizer
"Good mix of topics. Very good range of relevant subjects with good speaker knowledge."- MSD

Advisory Board:

View snapshot of speakers

Featured Webinar

webinar

PANEL: Addressing Compatibility Issues between Suppliers – will we ever see harmonisation?
This panel brings together two leading industry experts to address the challenges of integration between different vendor technologies and how to asses compatibility. Flexibility and the ability to work with multiple suppliers is a crucial factor in the decision to switch to single use and how and when to implement. Take the chance to listen to how they are planning to achieve harmonisation as well as questions form the live audience...

Panelists:

steven Stephen Brown
CTO
Vivalis

jerry Jerold Martin
Chairman of the Board
BPSA


 
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Interested in sponsorship?

Contact Sarah Strangeways on +44 (0)207 368 9300 or sponsorship@iqpc.co.uk for more details about sponsoring or exhibiting.

If you didn’t make it last year, here is a synopsis form last year’s chairman…

“On February 1–2, 2011, I visited Brussels to chair the International Quality and Productivity Center's (IQPC) Pharma–IQ Disposables Solutions for Biomanufacturing Conference, which was attended by nearly 100 European manufacturers and suppliers. The conference was Pharma–IQ's third Annual European Disposables meeting. The previous two annual conferences were held in London, and the event is shaping up to be a key European conference for single-use activities. This year's meeting featured speakers from several European-based vaccine, biopharmaceutical, and contract manufacturers, including Novartis, Vivalis, Genzyme, CMC Biologics, Cobra Biomanufacturing, Innogenics, Crucell, Eli Lilly, GlaxoSmithKline, Pfizer, and Merck Serono, along with supplier presentations from Pall Life Sciences, Sartorius-Stedim Biotech, Novasep, JM Bioconnect, GE Healthcare, and ATMI Life Sciences.

National European regulatory authorities and the European Medicines Agency have not made public statements about the acceptability or requirements for single-use technologies, but this has not deterred European drug sponsor and contract manufacturing facilities from implementing such systems for both clinical and production batches. Conference topics, for example, focused on everything from comparability of product quality and reduction of carbon footprints to implementation of single-use systems for buffer filling processes and preparation of regulatory submissions. The conference also featured several roundtable discussion sessions that facilitated the sharing of questions and experiences among participants.”

Jerold Martin, Senior Vice-President of Global Scientific Affairs, Pall Life Sciences, and Chairman of the Board and Technology Committee, Bio-Process Systems Alliance

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