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The Global Health Medical Device Compendium is an inventory of '''medical devices designed for use and/or implemented within resource-limited settings'''.  
The [[Global Health Medical Device Compendium]] is an inventory of '''medical devices designed for use and/or implemented within resource-limited settings'''.  


The compendium is sortable by '''health topic''' (e.g., Malaria and HIV/AIDS), '''classification''' (i.e., Preventative, Diagnosis or Treatment), '''scope''' (i.e., Prototype, Clinical trial, Commercialized) and '''location''' (by continent).
The compendium is sortable by '''health topic''' (e.g., Malaria and HIV/AIDS), '''classification''' (i.e., Preventative, Diagnosis or Treatment), '''scope''' (i.e., Prototype, Clinical trial, Commercialized) and '''location''' (by continent). New devices can be added using [[Form:Medical Device]].
 
The [[Global Health Medical Device Compendium]] is the work of Prof. Kathleen Sienko and her graduate students, and the Center for Global Health Student Associates at the University of Michigan. New devices can be added using [[Form:Medical Device]].


The following table shows three devices per medical topic. You can also {{#drilldownlink:category=Medical_Devices|single|link text=drill down by topic, classification, scope and/or location}}.
The following table shows three devices per medical topic. You can also {{#drilldownlink:category=Medical_Devices|single|link text=drill down by topic, classification, scope and/or location}}.
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[[Category:Global Health Medical Device Compendium]]
[[Category:Global Health Medical Device Compendium]]
[[Category:Portals]]
[[Category:Portals]]
A whole range of regulatory and non-regulatory documents is required during clinical trials. The success of drug approval hinges on the quality of these documents – and this is where the Medical of CRS comes in.
The Medical offers expert services ranging from preparing individual documents to producing all the documents needed for the draw up, coordination and documentation of clinical trials in a scientifically accurate way. Thanks to their extensive experience the professionals in the Medical understand how to meet challenging timelines and to crystallise the essential data. They are able to integrate clinical and operational data into concisely written, well structured documents complying with current regulations and guidelines. The bottom line is that CRS makes sponsors' clinical trial documentation more efficient, saving both time and money.

Revision as of 04:20, 26 February 2016

The Global Health Medical Device Compendium is an inventory of medical devices designed for use and/or implemented within resource-limited settings.

The compendium is sortable by health topic (e.g., Malaria and HIV/AIDS), classification (i.e., Preventative, Diagnosis or Treatment), scope (i.e., Prototype, Clinical trial, Commercialized) and location (by continent). New devices can be added using Form:Medical Device.

The following table shows three devices per medical topic. You can also {{#drilldownlink:category=Medical_Devices|single|link text=drill down by topic, classification, scope and/or location}}.

Usage

Portals

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