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MDB
(redirected from Medical Devices Bureau)

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AcronymDefinition
MdBMitglied des Bundestages (German: Member of Parliament)
MDBMicrosoft Access Database (file extension)
MDBMessage Driven Bean
MDBMurray-Darling Basin (South Australia)
MDBModular Debugger
MDBMultilateral Development Bank
MDBMy Dying Bride (band)
mdBMit der Bitte (German: With the Request)
MDBManagement Database
MDBMaster Database
MdBMovimento Democrático Brasileiro (Brazilian party)
MDBMoscow Defense Brief
MDBMulti Drop Bus
MDBMarketing Database
MDBMetalloprotein Database and Browser
MDBMouvement de Defense de la Bicyclette (French)
MDBMetropolitan Development Board
MDBMurder by Death (band)
MDBMedical Devices Bureau (Health Canada)
MDBMillion Dollar Band (University of Alabama, Tuscaloosa, Alabama)
MDBMutual Defense Board (United States of America and the Republic of the Philippines)
MDBMaintenance Database
MDBMy Data Bank (software feature)
MDBMicroarray Database
MDBMain Distribution Board
MDBMelbourne Development Board (Melbourne, Australia)
MDBMarc Douglas Berardo (singer/songwriter)
MDBMesh Database
MDBMestské divadlo Brno (Brno City Theatre; Brno, Czech Republic)
MDBMission Data Base
MDBMichiel de Boer (artist webstite)
MDBBasic Metal Detector
MDBMovable Deformable Barrier (automobile crash testing)
MDBManufacturing Data Base
MDBMulticast Descriptor Block (Cisco)
MDBMaximum Death Benefit (insurance)
MDBMusical Data Bases
MDBMississippi Delta Blues (Society)
MDBMaintenance Manual Depot With IPB
MDBManagement Data Bank
MDBMaintenance Decision Board
MDBMolecular Diagnostics and Biotechnology
MDBMarsavius Design Bureau
MDBMultiplex Data Bus
MDBMaximum Delay Bounds
MDBMultipoint Data Bridging
MDBMillennium Dome Bombing


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? References in periodicals archive
28) The regulations, which are administered by the Medical Devices Bureau (
Canadian legal oversight of pharmacogenomics and nutrigenomics by Morin, Karine / Health Law Review
The agency's quality requirements and ISO 13485 standards demand that companies control suppliers' quality but don't provide guidance as to how that should be accomplished; Egan Cobbold, quality systems officer with Health Canada's Medical Devices Bureau and chair of the Global Harmonization Task Force (GHTF) Study Group 3 (SG3), predicted that the guidance document the group expects to post for public comment in June will answer many of those questions.
A quality eye on suppliers: as global regulatory bodies take a harder ... by Weaver, Allison / Medical Product Outsourcing
The Medical Devices Bureau has indicated that the informal appeal procedure may consist of two steps: first, speaking with the direct manager of the inspector requesting the recall; second, if the matter remains unresolved, speaking with the manager of the Operational Centre at which the inspector works.
Recalls of Medical Devices Imposed by Health Canada: The Legal ... by Kisluk, Michelle; VanderElst, Ingrid / Mondaq Business Briefing
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