MedTech Summit US

Description

The MedTech Summit US is dedicated to EU MDR implementation, FDA policy and digital health.

The MedTech Summit US covers topics such as:

  • Imperatives for clinical and post market surveillance requirements under the EU MDR and achieve compliance
  • EU MDR implementation status, the latest requirements and advice for industry
  • How global quality requirements are being streamlined as the FDA aligns with ISO 13485
  • Industry case studies and detailed discussion on EU MDR challenges and opportunities
  • Real-World Evidence to fulfill reimbursement requirements
  • What steps you should take to ensure 510K device approval
  • Ideas from industry peers on gaining regulatory approval for software
  • FDA regulatory initiatives for software, AI and cyber security
  • Security, quality and risk best practice

The MedTech Summit US brings together attendees with responsibilities in:

  • Quality
  • Regulatory Affairs
  • Clinical
  • Software
  • Vigilance and Medical Safety
  • Post Market Surveillance
  • Medical Device

Future Events

Past Events

Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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