Plastics in Medical Devices 2008
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ProgrammeSessionList
PROGRAMME

Day Two

Thursday, 10th April 2008

08:30
Registration and coffee

09:15
Chairman’s opening remarks
 
CHRIS SMITH, Editor and Conference Manager
EUROPEAN PLASTICS NEWS

09:30
The DEHP debate
  • Labelling of medical devices
  • Alternative plasticisers
DAVID CADOGAN, Director
EUROPEAN COUNCIL FOR PLASTICISERS AND INTERMEDIATES (ECPI)

10:00
CASE STUDY: Alternative to phthalates
  • How concerns and political initiatives influence typical medical device manufacturers
  • How manufacturers of medical tubing react when politicians, NGO’s and hospitals ask for alternatives to phthalates
  • Alternatives in the market
    • can they do the job?
    • are they better than phthalates?
OLE GRØNDAHL HANSEN, General Manager
PVC INFORMATION COUNCIL DENMARK

10:30
END-USER PERSPECTIVE: Drug device interactions in an inhalation product
  • Drug formulation
  • Interactions generated
  • Managing the performance limiting effect
OREST LASTOW, Pharmaceutical and Analytical R&D
ASTRAZENECA

11:00
Question and answer session

11:10
Coffee

11:40
Sustained success through automation
  • Insight into the correct way to implement a fully automated in-line process to the moulding of medical products
    • the right approach to projects
    • turning concepts into running systems
    • FMEA & Validation
    • case study of a medical moulder
ANDY SARGISSON, Export Sales Director
WALDORF TECHNIK

12:10
Design for manufacture
  • Design for manufacture in 2008 and beyond
  • Adding value and reducing waste
  • Advantages of integrated product creation with a manufacturing partner
  • Case study: HPV DNA Sampling Device (Cervical Screening)
MIKE SULLIVAN, Director Engineering & Operations Improvement
ROSTI TECHNICAL PLASTICS

12:40
Integrating human sciences, design and engineering in medical device design and development
  • Defining the relationship between people, products and environments of use
  • The role Human Factor Engineering (HFE) plays in risk management and regulatory compliance
  • The value of user validation throughout the product development process
  • Product examples that illustrate the benefits of this integrated approach
ALUN WILCOX, Director of Medical
PDD DESIGN

13:10
Question and answer session

13:20
Lunch

14:30
CASE STUDY: General process of the selection of materials for medical devices application
 
VINCENT STÉPHENNE, Product Development Manager
BAXTER R&D EUROPE

15:00
Sterilisation and the material selection process
  • Multi-component injection moulding
  • In-mould decoration and in-mould assembly
  • Ceramic injection moulding
  • Polymer bonded magnets
BRAM JONGEN, Technical Support Manager
HELVOET PHARMA

15:30
Innovation moulding processes for medical applications
  • The difference between the EU and the rest of the world (US/Europe) regarding medical devices
  • Product liability
  • Conformity
  • Biocompatibility
DIETMAR DRUMMER, Head of Technology Management
MANFRED RIEHL, Head of Business Unit
OECHSLER AG

16:00
Question and answer session

16:15
Chairman’s closing remarks and end of conference

Click here for Day One

 
 
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