MDCG Guidance on Qualification and Classification of Annex XVI Products: Overview and Qualification | EU
Source Node: 2542990
Time Stamp: Apr 12, 2024
Reg Desk
HSA Guidance on Medical Device Product Registration: Specific Aspects | HSA
Source Node: 2542992
Time Stamp: Apr 12, 2024
SFDA Guidance on In-House IVDs: Intended Use and Risks | SFDA
Source Node: 2544108
Time Stamp: Apr 12, 2024
Health Canada Guidance on Management of Medical Device Applications: Review Process | RegDesk
Source Node: 2544110
Time Stamp: Apr 12, 2024
SFDA Guidance on In-House IVDs: Specific Aspects | SFDA
Source Node: 2547585
Time Stamp: Apr 12, 2024
IMDRF Guide on Adverse Event Reporting Terminology: Overview | RegDesk
Source Node: 2547587
Time Stamp: Apr 12, 2024
IMDRF Guide on Adverse Event Reporting Terminology: Details | RegDesk
Source Node: 2548688
Time Stamp: Apr 12, 2024
TGA Guidance on Conformity Assessment Certification Applications | TGA
Source Node: 2548690
Time Stamp: Apr 12, 2024
FDA Draft Guidance on Section 524B: Overview | United States
Source Node: 2538795
Time Stamp: Apr 8, 2024
FDA Draft Guidance on Section 524B: Documentation | United States
Source Node: 2538797
Time Stamp: Apr 8, 2024
FDA Draft Guidance on Section 524B: Specific Aspects | United States
Source Node: 2539641
Time Stamp: Apr 8, 2024
TGA Consultation on CDSS Software Regulation: Overview | TGA
Source Node: 2539643
Time Stamp: Apr 8, 2024
TGA Consultation on CDSS Software Regulation: Problems and Proposals | TGA
Source Node: 2541780
Time Stamp: Apr 8, 2024
FDA Draft Guidance on Q-Submission Program: Overview | United States
Source Node: 2541782
Time Stamp: Apr 8, 2024
MDCG Guidance on Content of Clinical Investigation Plan: Specific Aspects | EU
Source Node: 2533827
Time Stamp: Apr 1, 2024
Health Canada Guidance on Management of Medical Device Applications: Overview | RegDesk
Source Node: 2533829
Time Stamp: Apr 1, 2024
DRAP Draft Guidance on Clinical Research: Final Reporting | Pakistan
Source Node: 2517377
Time Stamp: Mar 14, 2024
Health Canada Guidance on Medical Device Recalls: Overview | RegDesk
Source Node: 2517379
Time Stamp: Mar 14, 2024