Plastics in Medical Devices 2008
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ProgrammeSessionList
PROGRAMME

Day One

Wednesday, 9th April 2008

08:30
Registration and coffee

09:20
Chairman’s opening remarks
 
CHRIS SMITH, Editor and Conference Manager
EUROPEAN PLASTICS NEWS

09:30
Current and future trends in the plastics in medical devices industry
  • Minimum invasive surgical devices
  • Microfluids
  • Single-use devices
  • Diagnostics
  • Regulatory/legislation aspects in relation to:
    • medical devices and the approach to healthcare materials
    • raw materials
FRITZ MAIER, Europe Market Development Manager
UNIVAC PRECISION ENGINEERING PTE LTD

10:00
Effective selection of plastics for medical devices
  • Basic principles for biocompatible plastics selections
  • Understanding the implication of ISO 10993 and other biocompatibility standards
  • How to select a test program for final devices
  • Screening test and principal steps for the characterisation of plastic raw materials
    • how to minimise compliance testing
JEAN-PIERRE BOUTRAND, General Manager, Scientific Director
BIOMATECH

10:30
From materials to application
  • Material/application requirements and application development
  • Co-operation with different partners in the supply chain
  • Examples of specific healthcare applications
 
 
Mr HANS MELIO, Managing Director
GL Plastics
JAN-WILLEM DEN HOLLANDER, Sales Engineer
GL PLASTICS

11:00
Question and answer session

11:10
Coffee

11:40
Function follows design: Future packaging and devices in the medical devices and pharmaceutical industry
  • Trends in the medical device and pharmaceutical industry
  • Add-on decoration
  • Technologies to attract packaging and devices
  • Case studies
  • Outlook
HARALD GRÜN, Sales & Marketing Director
BALDA MEDICAL

12:10
The use of novel polymers
  • Potential applications
    • synthesis, processing and surface modifications
    • high temperature thermoplastics, elastomers, rubbers, electroactive, etc
    • surface modifications for improved biocompatibility
    • improvements in plant-derived and degradable polymers to allow use in medical devices and packaging
KARL KRATZ, Head of Analytics Department
INSTITUTE OF POLYMER RESEARCH

12:40
Rational selection of plastics and elastomers for medical devices and supplies
  • Why is it not easy to select polymers in a systematic manner?
  • Where can we get data from?
    • what are the limitations of typical data sources?
    • how can the limitations be overcome?
  • How do we account for materials attributes, like biocompatibility and sterilisability, that are important for medical applications?
  • How can we trade-off cost, mass, size and performance in design?
  • How do we provide accurate data for CAE?
PATRICK COULTER, Chief Operating Officer
GRANTA DESIGN

13:10
Question and answer session

13:20
Lunch

14:30
CASE STUDY: Innovative thermoplastics materials for healthcare applications
  • Macro trends:
    • expansion and aging of the population
    • identification of new health issues
    • efficient management of patient care
    • environmental responsibility
  • Selecting the right materials for an expanding set of application requirements
  • Demonstrating the potential capabilities of specific materials in a diverse range of healthcare applications
ROB DE JONG, Industry Manager Healthcare
SABIC INNOVATIVE PLASTICS

15:00
Sustainable polymers and plastics through green chemistry
  • Drivers for change in chemicals and plastics
  • Principles of green chemistry and sustainable development
  • Challenges and opportunities across the product lifecycle
  • Green chemistry opportunities for materials design and preparation
  • Biorefinaries and new green and sustainable products from biomass
JAMES CLARK, Professor of Chemistry and Director of Green Chemistry
CENTRE OF EXCELLENCE

15:45
Question and answer session

15:55
Tea

16:15
Thermoplastic elastomer compounds from a medical perspective
  • Exploring the possibilities of styrenic based thermoplastic elastomer (TPE) compounds in medical applications
  • Aspects of TPE compounds and compounding as seen from a medical perspective
    • raw material selection
    • cleanliness
    • traceability
    • reproducibility and compounding equipment requirements
    • formulation change notification
  • Considerations when running a medical grade TPE development project
NIKLAS OTTOSSON, Technical Manager Medical
VTC TPE GROUP

16:45
Efficient procedures from innovation to mass production of medical devices
  • Analysing of innovation
  • Efficient development work to shorten leadtime
  • Short delivery times of tooling
  • High quality design of experiment (DOE)
  • Flexible automation
JOHAN LINDQVIST, Business Manager Pharma, Chemical Engineer
MEDIFIQ

17:15
Question and answer session

17:30
Chairman’s closing remarks and end of Day One

19:00
Conference dinner for all delegates and speakers
Informal networking dinner (included in the delegate fee)

Click here for Day Two

 
 
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