Attestato di partecipazione
- Cinical Affairs staff
- Regulatory Affairs professionals
- Medical Writer
- Quality system and quality assurance personnel
- Technical and Medical Writers
- CROs
- Those who conduct clinical evaluations/investigations/post-market follow-up studies
- Professionals moving from pharmaceuticals to medical devices
Register
Printable Version
At the end of the training path, you will be able to
Appropriately address the requirements for clinical evaluation for all classes of devices, regardless of risk classification
Know how to establish measurable endpoints for clinical claims and guide a straight-forward literature search and source additional data
Know how to avoid common pitfalls when addressing the benefit/risk profile of your medical device and be compliant with related requirements
Online interactive masterclass on Zoom platform.
LS Academy will provide the access link to the virtual platform a few days before each training.
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