I3CGlobal FDA 510k February 6, 2025 FDA 510k for Toxoplasma Gondii Serological Reagents ... Read More
I3CGlobal FDA 510k, Labelling, Medical Device February 5, 2025 The Critical Role of Labeling Requirements For Orthopedic Implants ... Read More
I3CGlobal FDA 510k February 5, 2025 Software Medical Device Documentation for 510(k) Submissions ... Read More
I3CGlobal FDA 510k, IVDR, Medical Device February 4, 2025 Labeling Requirements of In Vitro Diagnostic Medical Devices (IVD) – FDA 510k Perspective ... Read More
I3CGlobal Clinical Evaluation February 3, 2025 The Role of CER in Mitigating Device Recalls and Withdrawals ... Read More
I3CGlobal FDA, FDA 510k, Medical Device January 31, 2025 510k Pathway for Active Implantable Medical Devices ... Read More
I3CGlobal FDA, FDA Food Registration January 30, 2025 FDA Establishment Registration and Device Listing ... Read More
I3CGlobal FDA, FDA 510k, IVDR January 30, 2025 Shelf Life Stability Studies for IVDs: Crucial Requirements for FDA 510(k) Compliance ... Read More
I3CGlobal FDA, FDA 510k, Medical Device January 30, 2025 Electrical Safety in Medical Devices For FDA 510K Submission ... Read More