Medtech Matters

153 Episoder

1. 3D Printing Healthcare at the Point of Care

   Publisert: 23.3.2018
2. Quality vs. Regulatory

   Publisert: 2.3.2018
3. The 'New' Alternative 510k

   Publisert: 29.1.2018
4. Regulatory Approval Pathway for Biomaterials

   Publisert: 2.1.2018
5. Pre-Sub with the FDA

   Publisert: 6.11.2017
6. Human Factors

   Publisert: 9.10.2017
7. MDUFA IV and Its Impact on Medtech Innovation

   Publisert: 7.9.2017
8. Off-Label Use

   Publisert: 25.8.2017
9. Biomaterials, Biocompatibility, and Bioabsorbable

   Publisert: 24.7.2017
10. 3D Printing in Healthcare

    Publisert: 5.6.2017
11. Reimbursement for Engineers

    Publisert: 5.5.2017
12. Device Incident Reporting

    Publisert: 30.3.2017
13. Real World Evidence

    Publisert: 24.2.2017