| 08:15 |
Registration & Welcome Coffee |
| 09:00 |
Opening words from our Chairman |
| 09:15 |
“Biocompatibility: Understanding the new ISO 10993” |
| 10:00 |
“Ethylene Oxide Sterilisation: The sustainable development & validation of effectives processes” |
| 10:45 |
Networking break & Beverages |
| 11:00 |
“Additive Manufacturing (3D Printing) Microbiological Considerations for DePuy Synthes Resorbable Polymeric Patient Specific Implant” |
| 12:00 |
Lunch break, 1 to 1 expert consultations & Opportunity to visit Swiss Medtech (1h30) |
| 13:30 |
“Regulatory requirements for sterile packaging with focus on the new ISO 11607:2019” |
| 14:15 |
“Complying with the European Union’s MDR”
|
| 15:00 |
“EU’s MDR and its impact on tests, validations and biological evaluation for Medical devices (transient use), implants and surgical instruments. An overview.”
|
| 15:45 |
Closing words from our Chairman
|
| 16:00 |
Consult the Experts & Networking Aperitif, 1 to 1 session, bring your samples for advices on packaging, validation, biocompatibility, CE, regulatory requirements.
|
| 19:30 |
Closing |
