I3CGlobal FDA, FDA 510k January 30, 2025 Medical Device Labeling: A Key Requirement for 510k ... Read More
I3CGlobal IVDR, Medical Device January 29, 2025 Next Generation Sequencing: 510k Regulatory Considerations for Genomic Diagnostics ... Read More
I3CGlobal Post Market Surveillance January 25, 2025 Post Market Surveillance Data in Clinical Evaluation Reports ... Read More
I3CGlobal Clinical Evaluation January 24, 2025 Differences Between Class I, IIa, IIb, and III Medical Devices in Terms of Clinical Evaluation Report ... Read More
I3CGlobal PMCF January 24, 2025 The Role of PMCF in Transitioning Legacy Devices from MDD to MDR ... Read More
I3CGlobal PMCF, Post Market Surveillance, PSUR January 24, 2025 Role of Post Market Clinical Follow Up In Vigilance System and Incident Reporting ... Read More
I3CGlobal Unique Device Identification January 24, 2025 UDI (Unique Device Identification): Ensuring Traceability and Compliance in the EU Market Introduction ... Read More
I3CGlobal FDA, FDA 510k, Medical Device January 24, 2025 Software in a Medical Device Existing Changes: 510k Submission Decision-Making ... Read More
I3CGlobal Clinical Evaluation January 24, 2025 Clinical Evaluation vs Clinical Investigations ... Read More
