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Test 1 Acronyms
Test 1: Documentation, Validation, Research Facility
34
Pharmacology
Undergraduate 3
01/28/2015
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Term
GMP
 Definition
Good Manufacturing Practices
Term
CGMP
 Definition
Current Good Manufacturing Practices
Term
TOC
 Definition
Total Organic Carbon
Term
CFR
 Definition
Code of Federal Regulations
Term
FDA
 Definition
Food and Drug Administration
Term
GLP
 Definition
Good Laboratory Practice
Term
GCP
 Definition
Good Clinical Practice
Term
EPA
 Definition
Environmental Protection Agency
Term
OSHA
 Definition
Occupational Safety and Health Administration
Term
SOP
 Definition
Standard Operating Procedures
Term
CAPA
 Definition
Corrective and Preventative Action
Term
OTC
 Definition
Over the Counter
Term
CIP
 Definition
Clean in Place
Term
COP
 Definition
Clean Out of Place
Term
DQ
 Definition
Design Qualification
Term
IQ
 Definition
Installation Qualification
Term
OP
 Definition
Operational Qualification
Term
PQ
 Definition
Performance Qualification
Term
EDR
 Definition
Enhanced Design Review
Term
FAT
 Definition
Factory Acceptance testing
Term
SAT
 Definition
Site Acceptance Testing
Term
FDS
 Definition
Functional Design Specification
Term
HPLC
 Definition
High Performance Liquid Chromatography
Term
HVAC
 Definition
Heating, Ventilation, and Air Conditioning
Term
OOS
 Definition
Out of Specification
Term
P&IDs
 Definition
Piping and Instrumentation Diagrams
Term
PV
 Definition
Process Validation
Term
QA
 Definition
Quality Assurance
Term
QC
 Definition
Quality Control
Term
R&D
 Definition
Research & Development
Term
SME
 Definition
Subject Matter Expert
Term
URS
 Definition
User Requirement Specification
Term
UV
 Definition
Ultraviolet
Term
VMP
 Definition
Validation Master Plan
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