Medical Regulations Info Day
Event details
| Date | 05.02.2015 |
| Location | |
| Category | Conferences - Seminars |
Nano-Tera.ch Info Day
Several Nano-Tera projects are tackling medical issues and may need to address medical regulations. As a researcher, it is difficult to know which regulations apply, at what time in the project and how to address them.
As a consequence, Nano-Tera is organizing an information day about these important issues. It will present an overview of the medical regulations (laws, CE Marking, FDA approval, GMP’s, GLP’s, Pre-Clinical Testing, Clinical Evaluation…), notifying bodies and competent authorities (Swissmedic, ethical committees, FDA, TÜV, etc…). It will also help in classifying the research activity according to applicable regulations (well-being, diagnostics, treatment, implants, etc.).
A large time slot will be devoted to Q&A.
A detailed program will follow. Please register here.
Several Nano-Tera projects are tackling medical issues and may need to address medical regulations. As a researcher, it is difficult to know which regulations apply, at what time in the project and how to address them.
As a consequence, Nano-Tera is organizing an information day about these important issues. It will present an overview of the medical regulations (laws, CE Marking, FDA approval, GMP’s, GLP’s, Pre-Clinical Testing, Clinical Evaluation…), notifying bodies and competent authorities (Swissmedic, ethical committees, FDA, TÜV, etc…). It will also help in classifying the research activity according to applicable regulations (well-being, diagnostics, treatment, implants, etc.).
A large time slot will be devoted to Q&A.
A detailed program will follow. Please register here.
Practical information
- General public
- Free
Organizer
- Martin Rajman
Contact
- Jocelyne Vassalli