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| + | [[Category:RCRIM]] | ||
| + | [[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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== Glossary of Abbreviations and Terms == | == Glossary of Abbreviations and Terms == | ||
| − | *[[Abbreviated New Drug Application]] (ANDA) | + | *[[Abbreviated New Drug Application]] ([[ANDA]]) |
| − | *[[Annotated ECG]] (aECG) | + | *[[Annotated ECG]] ([[aECG]]) |
*[[Application (RPS)|Application]] | *[[Application (RPS)|Application]] | ||
*[[Application Number]] | *[[Application Number]] | ||
*[[Approval (RPS)|Approval]] | *[[Approval (RPS)|Approval]] | ||
*[[Approval Unit (RPS)|Approval Unit]] | *[[Approval Unit (RPS)|Approval Unit]] | ||
| − | *[[Board of Health]] (BoH) | + | *[[Board of Health]] ([[BoH]]) |
| − | *[[Chemistry, Manufacturing and Controls]] (CMC) | + | *[[RPS Hyperlinking|Broken Links]] ([[RPS Hyperlinking]]) |
| − | *[[Center for Devices and Radiological Health]] (CDRH) (FDA) | + | *[[Chemistry, Manufacturing and Controls]] ([[CMC]]) |
| − | *[[Center for Food Safety and Applied Nutrition]] (CFSAN) (FDA) | + | *[[Center for Devices and Radiological Health]] ([[CDRH]]) (FDA) |
| + | *[[Center for Food Safety and Applied Nutrition]] ([[CFSAN]]) (FDA) | ||
| + | *[[Contact Type (RPS)|Contact Type]] | ||
*[[Context of Use (RPS)|Context of Use]] | *[[Context of Use (RPS)|Context of Use]] | ||
| + | *[[Correspondence (RPS)|Correspondence]] | ||
*[[Document (RPS)|Document]] | *[[Document (RPS)|Document]] | ||
*[[Document Reference (RPS)|Document Reference]] | *[[Document Reference (RPS)|Document Reference]] | ||
*[[Document Relationship (RPS)|Document Relationship]] | *[[Document Relationship (RPS)|Document Relationship]] | ||
| − | *[[Drug Master File]] (DMF) | + | *[[Dossier]] - Generalized synonym for RPS [[Application (RPS)|Application]] concept |
| − | *[[Electrocardiogram]] (ECG) | + | *[[Drug Master File]] ([[DMF]]) |
| − | *[[European Union]] (EU) | + | *[[Electrocardiogram]] ([[ECG]]) |
| + | *[[European Union]] ([[EU]]) | ||
*[[External Electronic Source (RPS)|External Electronic Source]] / non-retrievable | *[[External Electronic Source (RPS)|External Electronic Source]] / non-retrievable | ||
| − | *[[Food and Drug Administration]] (FDA) (US) | + | *[[File (RPS)|File]] |
| + | *[[Food and Drug Administration]] ([[FDA]]) (US) | ||
*[[Holder of Reference Master File]] | *[[Holder of Reference Master File]] | ||
| − | *[[Investigational New Drug]] (IND) | + | *[[RPS Hyperlinking|Hyperlinking]] |
| − | *[[Investigator Brochure]] (IB) | + | *[[International Conference on Harmonisation]] ([[ICH]]) |
| + | *[[Investigational New Drug]] ([[IND]]) | ||
| + | *[[Investigator Brochure]] ([[IB]]) | ||
*[[Keyword (RPS)|Keyword]] | *[[Keyword (RPS)|Keyword]] | ||
*[[Master Access File]] | *[[Master Access File]] | ||
*[[Master File Holder]] | *[[Master File Holder]] | ||
*[[Member State]] | *[[Member State]] | ||
| − | *[[New Drug Application]] (NDA) | + | *[[Message (RPS)|Message]] |
| − | *[[Periodic Safety Update Report]] (PSUR) | + | *[[New Drug Application]] ([[NDA]]) |
| + | *[[Package (RPS)|Package]] - Generalized synonym for RPS [[Submission Unit (RPS)|Submission Unit]] concept | ||
| + | *[[Periodic Safety Update Report]] ([[PSUR]]) | ||
*[[Phase I Meeting]] | *[[Phase I Meeting]] | ||
*[[Phase II Meeting]] | *[[Phase II Meeting]] | ||
*[[Post-market]] | *[[Post-market]] | ||
*[[Pre-submission]] | *[[Pre-submission]] | ||
| + | *[[Product (RPS)|Product]] | ||
| + | *[[Regulated Industry]] | ||
*[[Regulated Product (RPS)|Regulated Product]] | *[[Regulated Product (RPS)|Regulated Product]] | ||
| − | *[[Regulated Product | + | *[[Regulated Product Submissions]] (RPS) |
| + | *[[Regulatory Activity]] -- Generalized synonym for RPS [[Submission (RPS)|Submission]] | ||
*[[Regulatory Authority (RPS)|Regulatory Authority]] | *[[Regulatory Authority (RPS)|Regulatory Authority]] | ||
*[[Reviewable Unit (RPS)|Reviewable Unit]] | *[[Reviewable Unit (RPS)|Reviewable Unit]] | ||
*[[Right of Reference Request]] | *[[Right of Reference Request]] | ||
| + | *[[Sponsor (RPS)|Sponsor]] | ||
*[[Submission (RPS)|Submission]] | *[[Submission (RPS)|Submission]] | ||
*[[Submission Unit (RPS)|Submission Unit]] | *[[Submission Unit (RPS)|Submission Unit]] | ||
| − | *[[ | + | *[[Submission Unit Type (RPS)|Submission Unit Type]] |
| − | *[[Supplemental New Drug Application]] (sNDA) | + | *[[Supplemental New Drug Application]] ([[sNDA]]) |
| − | *[[Table of Contents]] (TOC) | + | *[[Table of Contents]] ([[TOC]]) |
| − | *[[Threaded | + | *[[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
- Abbreviated New Drug Application (ANDA)
- Annotated ECG (aECG)
- Application
- Application Number
- Approval
- Approval Unit
- Board of Health (BoH)
- Broken Links (RPS Hyperlinking)
- Chemistry, Manufacturing and Controls (CMC)
- Center for Devices and Radiological Health (CDRH) (FDA)
- Center for Food Safety and Applied Nutrition (CFSAN) (FDA)
- Contact Type
- Context of Use
- Correspondence
- Document
- Document Reference
- Document Relationship
- Dossier - Generalized synonym for RPS Application concept
- Drug Master File (DMF)
- Electrocardiogram (ECG)
- European Union (EU)
- External Electronic Source / non-retrievable
- File
- Food and Drug Administration (FDA) (US)
- Holder of Reference Master File
- Hyperlinking
- International Conference on Harmonisation (ICH)
- Investigational New Drug (IND)
- Investigator Brochure (IB)
- Keyword
- Master Access File
- Master File Holder
- Member State
- Message
- New Drug Application (NDA)
- Package - Generalized synonym for RPS Submission Unit concept
- Periodic Safety Update Report (PSUR)
- Phase I Meeting
- Phase II Meeting
- Post-market
- Pre-submission
- Product
- Regulated Industry
- Regulated Product
- Regulated Product Submissions (RPS)
- Regulatory Activity -- Generalized synonym for RPS Submission
- Regulatory Authority
- Reviewable Unit
- Right of Reference Request
- Sponsor
- Submission
- Submission Unit
- Submission Unit Type
- Supplemental New Drug Application (sNDA)
- Table of Contents (TOC)
- Threaded Discussions
