Statements (70)
| Predicate | Object |
|---|---|
| gptkbp:instance_of |
gptkb:organization
|
| gptkbp:addresses |
emerging technologies
|
| gptkbp:advocates_for |
regulatory science
|
| gptkbp:aims_to |
improve patient safety
|
| gptkbp:aims_to_improve |
market access
regulatory burden |
| gptkbp:collaborates_with |
gptkb:WHO
|
| gptkbp:composed_of |
member countries
|
| gptkbp:conducts |
workshops
|
| gptkbp:coordinates |
international efforts
|
| gptkbp:develops |
frameworks
|
| gptkbp:encourages |
innovation in medical devices
|
| gptkbp:enhances |
global health security
regulatory capacity |
| gptkbp:established |
gptkb:2011
|
| gptkbp:facilitates |
information sharing
|
| gptkbp:focus_area |
medical device regulation
|
| gptkbp:form |
gptkb:International_Medical_Device_Regulators_Forum
|
| gptkbp:fosters |
collaboration among regulators
|
| gptkbp:has_advisory_board |
expert panels
|
| gptkbp:has_publications |
gptkb:reports
|
| gptkbp:headquarters |
gptkb:Geneva,_Switzerland
|
| https://www.w3.org/2000/01/rdf-schema#label |
IMDRF
|
| gptkbp:is_a_resource_for |
guidance documents
|
| gptkbp:is_active_in |
gptkb:Africa
gptkb:Europe gptkb:Middle_East Americas Asia-Pacific region |
| gptkbp:is_engaged_in |
policy development
|
| gptkbp:is_focused_on |
patient-centered care
|
| gptkbp:is_involved_in |
gptkb:supply_chain_management
quality assurance regulatory compliance risk management capacity building clinical trials public health initiatives user training adverse event reporting product labeling market surveillance safety assessments post-market surveillance health economics health technology assessment clinical evaluations manufacturing standards device recalls device design device performance evaluation |
| gptkbp:is_organized_by |
several
|
| gptkbp:is_recognized_by |
global health organizations
|
| gptkbp:is_supported_by |
industry partners
|
| gptkbp:is_visible_from |
regulatory processes
|
| gptkbp:issues |
position papers
|
| gptkbp:meets |
gptkb:annually
|
| gptkbp:members |
regulatory authorities
|
| gptkbp:produces |
gptkb:guidelines
|
| gptkbp:promotes |
best practices
|
| gptkbp:provides |
technical assistance
|
| gptkbp:provides_support_for |
gptkb:medical_devices
|
| gptkbp:provides_training_for |
regulatory personnel
|
| gptkbp:purpose |
to accelerate international medical device regulatory harmonization
|
| gptkbp:supports |
regulatory convergence
|
| gptkbp:supports_harmonization_of |
gptkb:standard
|
| gptkbp:website |
www.imdrf.org
|
| gptkbp:works_with |
stakeholders
|
| gptkbp:bfsParent |
gptkb:ICMRA
|
| gptkbp:bfsLayer |
5
|