A strategy for integrating regulatory, reimbursement and outcomes research functions for effective market introduction of medical devices in the USA / DFAIT

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Achieving rapid market penetration and fair pricing for innovative medical technology In today's cost- conscious U.S. healthcare environment neceseitates a strategic approach to product development. While Food & Drug Administration (FDA) approval is adequate to establish product safety, healthcare coverage decisions made by payera such as Health Care Finance Administration (HCFA) or managed care plans are increasingly based on evidence of clinical effectiveness and improved patient outcome not to mention value and cost of delivery.

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Dernière modification avril 17, 2026, 20:25 (TU)
Créé le avril 17, 2026, 20:25 (TU)
contact_email opengovernment@international.gc.ca
criticality_level []
geographic_scope []
open_canada_collection publication
open_canada_date_published 1999-01-01 00:00:00
open_canada_keywords {"en": ["Government of Canada Publications", "United States", "Medical devices"], "fr": ["Publications du gouvernement du Canada", "États-Unis", "appareils médicaux"]}
open_canada_subject ["economics_and_industry", "government_and_politics", "health_and_safety"]
sensitivity_level unrestricted
title_fr Une stratégie d'intégration des questions de réglementation, de remboursements et des résultats des recherches, pour réussir à introduire avec succès des appareils médicaux sur le marché des États-Unis / MAECI
update_frequency not_planned