Difference between revisions of "RPS Glossary"

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[[Category:RCRIM]]
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[[Category:RPS]]
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[[Main Page]] | [[Regulated Clinical Research Information Management]] | [[Regulated Product Submissions]] | RPS Glossary
 
[[Main Page]] | [[Regulated Clinical Research Information Management]] | [[Regulated Product Submissions]] | RPS Glossary
  
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*[[Approval Unit (RPS)|Approval Unit]]
 
*[[Approval Unit (RPS)|Approval Unit]]
 
*[[Board of Health]] ([[BoH]])
 
*[[Board of Health]] ([[BoH]])
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*[[RPS Hyperlinking|Broken Links]] ([[RPS Hyperlinking]])
 
*[[Chemistry, Manufacturing and Controls]] ([[CMC]])
 
*[[Chemistry, Manufacturing and Controls]] ([[CMC]])
 
*[[Center for Devices and Radiological Health]] ([[CDRH]]) (FDA)
 
*[[Center for Devices and Radiological Health]] ([[CDRH]]) (FDA)
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*[[Food and Drug Administration]] ([[FDA]]) (US)
 
*[[Food and Drug Administration]] ([[FDA]]) (US)
 
*[[Holder of Reference Master File]]
 
*[[Holder of Reference Master File]]
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*[[RPS Hyperlinking|Hyperlinking]]
 
*[[International Conference on Harmonisation]] ([[ICH]])
 
*[[International Conference on Harmonisation]] ([[ICH]])
 
*[[Investigational New Drug]] ([[IND]])
 
*[[Investigational New Drug]] ([[IND]])
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*[[Supplemental New Drug Application]] ([[sNDA]])
 
*[[Supplemental New Drug Application]] ([[sNDA]])
 
*[[Table of Contents]] ([[TOC]])
 
*[[Table of Contents]] ([[TOC]])
*[[Threaded Discussion (RPS)|Threaded Discussion]]
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*[[RPS Threaded Discussions|Threaded Discussions]]

Latest revision as of 14:51, 25 August 2010


Main Page | Regulated Clinical Research Information Management | Regulated Product Submissions | RPS Glossary

This article is under construction

Please see the RPS Glossary Documentation page for instructions for creating and editing entries.

Glossary of Abbreviations and Terms