Due to unforeseen circumstances, we regret to announce Clinical Data Standardisation & Management 2011 event will not take place as planned on 06 - 08 June, 2011. We would like to thank you, our speakers and all those involved in supporting the event.

If you have any questions, we’d be happy to answer them – please contact us on:
Freephone: 0800 652 2363 or +44 (0)20 7368 9300

Email: enquire@iqpc.co.uk

Please see the following related events phase1clinicaldevelopment.com


Speakers

  • Phillippe Verplancke
    CDISC E3C Member, Managing Director
    XClinical GmbH
  • Peter Van Reusel
    CDISC E3C Member and Business Unit, Director of CRO Services
    Business & Decision
  • Herbert Noack
    Vice Chair, CDISC E3C Member & Project Statistician in Medical Affairs
    Boehringer Ingelheim
  • Jozef Aerts
    Founder, XML4Pharma and Volunteer
    CDISC
  • Andrew Miller
    Director of Clinical Data Standards
    AstraZeneca

Developing optimum strategies for improving clinical data management through CDISC standardisation, best-practice outsourcing, data warehousing and legacy data transformation

"The nicest thing about standards is that there are so many of them to choose from."

Andrew S. Tannenbaum

Pharma IQ is pleased to announce the dates for the 2nd annual Clinical Data Standardisation & Management Forum, taking place on the 7th - 8th June 2011, in London, UK.

As you are reading this, there are 350 clinical trials going on in the UK alone. Now imagine how many are happening in Europe. Now the world. That's a lot of man and computer hours, and a whole lot more data to collate, sort and analyse.

Along with regulatory expectations, credit crunching underfoot and the knives out and sharpened for cut-backs; efficiency and productivity have never been more important. Data standardisation is one of the ways these aims can be achieved.

Why Attend Clinical Data Standardisation & Management 2011:

  • The only event to provide you with CDISC and HL7 implementation strategies from no less than 11 pharma and bio companies
  • New for 2011: hear both the end-user and CRO perspective on how to practically implement a best practice outsourcing strategy and improve your internal processes as well
  • Find out about brand-new CDISC standards and how they apply to you - introducing a step-by-step workshop from the Europe’s primary registered CDISC trainer
  • Enjoy face-to-face interaction with industry experts like XML4Pharma’s Jozef Aerts, Business & Decision’s Peter Van Reusel, Genzyme’s Sue Dubman and AstraZeneca’s Andrew Miller

The hot topics at the event will include:

  • Understanding the latest CDISC initiatives from three CDISC E3C members
  • Optimising the sponsor/CRO relationship for the benefit of your organisation
  • Discovering the best-practice approach to the integration and uses of metadata repositories in clinical data management
  • Assessing the challenges and benefits of CDISC standardisation in both big and small pharma companies
  • Appreciating the business case for standardised clinical data within a pharma company
  • Examining the most important points to consider when offshoring statistical programming
  • Enhancing your data management capabilities through implementing data warehousing systems
  • Uncovering HL7 standardisation and its applications in the pharma and biotech industries

Don't miss out on our two pre-conference workshops with more than 7 hours of interactive content!

Workshop A: 10.00-13.30 CDISC Workshop – Introduction, Implementation and Future Developments

Workshop B:B 13.45 – 18.00 Integration and Interoperability: HL7 Workshop

Testimonials

What attendees of other Pharma IQ events have said:

“It was very valuable to have an overview about techniques which can be used and what basics are needed for this. It showed me that other pharmaceutical companies are faced with the same problems”.
Susanne Tollar, Solvay Pharmaceuticals
”Good balance between technical presentations and practical ones”.
Nuria Cubel Sune, Lab Esteve
”Interesting and willing to create discussion and to elaborate the presented themes. It was valuable”.
Isabel Sequeira, Hovione Farmaciencia SA
”I learned about some interesting new technologies and approaches”
Nuno Silva, Hovione Farmaciencia SA
”Good to meet the main players and have made contacts that I would not have made otherwise”.
Chris Christodoulou, Medimmune
Sponsor Media Partners
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