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2025
FDA | New Guidance Document for Section 506J of the FD&C Act

01-20
2025
AI-DSF Lifecycle Management&Marketing Submission Recommendations

01-20
2025
EU | Q&A on vigilance terms and concepts as outlined

01-20
2025
Health Canada Medical Device Registration Fees for FY2025

01-03
2025
EU | MDR Certification Process

01-03
2025
CCFDIE | 14th CIMDR Forum Held in Wuhan

01-03
2025
FDA | Global Unique Device Identification Database

01-03
2025
EU | Verification of Manufactured Class D IVDs by NB

01-03
2025
EU | Manufacturer Information Form

01-03
2025
Obligation in case of interruption or discontinuation of supply
