Competent Authority Update on Preparing for IVDR Clinical Performance Study Applications
$80 Per person
Critical Considerations in Site Selection and Subject Enrollment in Device and IVD Clinical Studies
$80 Per person
Competent Authority Expectations and Management of Device Clinical Study Applications Under the MDR
$70 Per person
Developing Clinical Investigation and Performance Study Plans That Meet Regulatory and Operational Requirements
$75 Per person
General Data Protection Regulations in the EU
$80 Per person
Aligning Clinical Investigations and Risk Management to Ensure MDR Compliance
$75 Per person
MDR Requirements for Sponsor GCP Inspections (audits) and How to Conduct Them
$70 Per person
Standards, Harmonisation Process and Common Specifications
$75 Per person
Software, Artificial Intelligence and Cybersecurity in the European Union
$75 Per person
Clinical Evaluation, Investigations and PMCF under MDR
$75 Per person
Major Regulatory Compliance Challenges for the Non-European Industry
$75 Per person
Benefit Risk Assessment
$75 Per person