The 8th Annual Medical Device Directives and The Revision 2014 is a conference that covers topics such as:
- Requirements for Post Market Clinical Follow-Up (PMCFU) and impact on industry
- New role of the "Qualified Person" (QP) and how to practically prepare for this requirement
- Regulation of software as a medical device in light of the revision of the MDD
- Changes to the current system in the proposal for reprocessing of single-use medical devices
- Changes associated with the Eudamed database and impacts on industry
- MDR requirement for implant cards
- The revision of the In Vitro Diagnostic Directive (IVDD)
The 8th Annual Medical Device Directives and The Revision 2014 brings together:
- Quality Assurance
- Regulatory Affairs
- Clinical Research
- Clinical Affairs
- Compliance
