Difference between revisions of "RPS Glossary"

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*[[European Union]] ([[EU]])
 
*[[European Union]] ([[EU]])
 
*[[External Electronic Source (RPS)|External Electronic Source]] / non-retrievable
 
*[[External Electronic Source (RPS)|External Electronic Source]] / non-retrievable
 +
*[[File (RPS)|File]]
 
*[[Food and Drug Administration]] ([[FDA]]) (US)
 
*[[Food and Drug Administration]] ([[FDA]]) (US)
 
*[[Holder of Reference Master File]]
 
*[[Holder of Reference Master File]]

Revision as of 19:46, 14 October 2008

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