EU Medical Device Coordination Group
GPTKB entity
Statements (64)
| Predicate | Object |
|---|---|
| gptkbp:instance_of |
gptkb:musical_group
|
| gptkbp:bfsLayer |
6
|
| gptkbp:bfsParent |
gptkb:European_Medical_Device_Regulation
|
| gptkbp:addresses |
safety concerns
|
| gptkbp:aims_to |
ensure safety and effectiveness of medical devices
|
| gptkbp:analysis |
device performance
|
| gptkbp:analyzes |
market surveillance data
|
| gptkbp:collaborates_with |
gptkb:legislation
|
| gptkbp:collaborations |
academic institutions
|
| gptkbp:communication |
manufacturers and regulators
|
| gptkbp:composed_of |
member states representatives
|
| gptkbp:conducts |
impact assessments
|
| gptkbp:contributed_to |
harmonization of medical device standards
|
| gptkbp:coordinates |
gptkb:European_Medicines_Agency
other regulatory bodies public consultations |
| gptkbp:depicted_in |
regulatory processes
|
| gptkbp:develops |
best practices
|
| gptkbp:discusses |
regulatory challenges
|
| gptkbp:encourages |
stakeholder engagement
|
| gptkbp:established |
EU Medical Device Regulation
|
| gptkbp:facilitates |
market access for medical devices
|
| gptkbp:feedback |
draft regulations
|
| https://www.w3.org/2000/01/rdf-schema#label |
EU Medical Device Coordination Group
|
| gptkbp:influences |
medical device policy
|
| gptkbp:input_output |
EU legislation
|
| gptkbp:is_a_framework_for |
device classification
|
| gptkbp:is_a_resource_for |
regulatory compliance
|
| gptkbp:is_evaluated_by |
new technologies
|
| gptkbp:issues |
regulatory matters
guidance documents emerging issues |
| gptkbp:legislation |
device safety
|
| gptkbp:meets |
regularly
|
| gptkbp:monitors |
compliance with regulations
|
| gptkbp:network |
industry stakeholders
|
| gptkbp:notifications |
safety issues
|
| gptkbp:organizes |
workshops
|
| gptkbp:part_of |
gptkb:legislation
|
| gptkbp:participates_in |
gptkb:international_forums
stakeholder consultations |
| gptkbp:performed_by |
clinical evaluation
|
| gptkbp:population_trend |
medical device market
|
| gptkbp:promotes |
innovation in medical devices
|
| gptkbp:provides |
expert advice
|
| gptkbp:provides_access_to |
information resources
|
| gptkbp:provides_information_on |
device registration
clinical evaluations medical device regulations post-market monitoring clinical investigations |
| gptkbp:regulates |
gptkb:hospital
|
| gptkbp:reports_to |
medical device incidents
|
| gptkbp:supports |
medical device safety
small and medium-sized enterprises notified bodies EU directives new regulatory frameworks |
| gptkbp:tactics |
risk management
|
| gptkbp:technology |
member states.
|
| gptkbp:training |
regulatory requirements
regulatory authorities |
| gptkbp:user_reviews |
gptkb:document
post-market surveillance |