The All New Content – More Than Just A Conference.
The MEDTEC Conference 2009 featured daylong sessions designed with extensive industry input and included a mix of senior-level professionals and experts within the medical manufacturing community: a learning experience about the best practices and processes which you will be able to immediately apply to your current responsibilities.
This year’s conference went beyond the standard model to not only educate but invite discussion and dialogue. Over the course of two days subjects like funding, regulatory and market analysis as well as a step by step guide to the medical device innovation process were presented.
Also new for this year were four in depth workshops on: Process Validation, Quality Systems, Supply chain and Testing and Reliability, lead by experienced professionals.
CONFERENCES |
| Wednesday, 23 September 2009 |
Funding, Regulatory and Market Analysis
• Double Presentation and Q&A: Leveraging the Science Foundation Ireland (SFI) investment; • Government Strategies to Support R&D by Multinational Companies in Ireland. • Double Presentation and Q&A: Venture Capital (VC) Funding for Medtech Companies. • Revolution in Healthcare - Future Technology Trends • Future of the Regulatory Framework for Medical Devices • Regulatory Framework for Combination Products in the EC • Strategies for Managing Intellectual Property Relating to Medical Devices |
| Thursday, 24 September 2009 |
Effective Medical Device and Diagnostic Development: A Road Map
• Phase I: Needs Assessment and Risk Analysis • Phase II: Formulation/Concept and Feasibility • Phase III: Design and Development/Verification and Validation • Phase IV: Final Validation/Product Launch Preparation • Phase V: Product Launch and Post Launch Assessment |
A CHOICE OF WORKSHOPS |
| Wednesday, 23 September 2009 |
Workshop 1: Process Validation: Solutions and Strategies for the Medical Device Industry
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