CDM Acronyms
ADaM - ANS -Analysis Data Model
- Analysis ready dataset, built from SDTM
AER - ANS -Adverse Event Report
AESI - ANS -Adverse Events of Special Interest
- Non-serious AEs which will be defined in the protocol for immediate reporting from investigator
to sponsor (within 24hrs of awareness), and are entered onto safety database
ALS - ANS -Architect Loader Spreadsheet
- Excel file
BAD - ANS -Biometrics Application Development
BAM - ANS -BioAnalytical Manager
BCE - ANS -Biometrics Computing Environment
BDL - ANS -Batch Data Loading
- Single push of data from one environment to another
BGPL - ANS -Biometrics Global Process Library
BOPM - ANS -Bioanalytical Operations Project Manager
BOR - ANS -Biosample Operations Responsible
BRIDG - ANS -Biometric Research Integrated Domain Group
BS - ANS -Biostatistics
BSO - ANS -Biometrics Strategic Operations
BV - ANS -Batch Validation
CASA - ANS -Clinical Application System Analyst
- System role withing Rave (CP)
CCDM - ANS -Clinical Coding & Dictionary Management
, CCS - ANS -Clinical Coding Specialist
CDASH - ANS -Clinical Data Acquisition Standards Harmonization
CDISC - ANS -Clinical Data Interchange Standards Consortium
CFDD - ANS -Custom Function Design Document
CFR - ANS -Code of Federal Regulation
CLT - ANS -Canadian Leadership Team
COLD - ANS -Collection Date
COREMAP - ANS -Corporate Records Management Programme
CP - ANS -Clinical Programmer
CPA - ANS -Clinical Programmer Analyst
cRMP - ANS -Core Risk Management Plan
CS - ANS -Clinician Scientist
CSIL - ANS -Clinical Study Implementation Leader
CSM - ANS -Country Study Manager
- Responsible for study performance within a single country
CSMS - ANS -Clinical Systems Management and Support
CSR - ANS -Clinical Study Report
- Summarizes all results from clinical study. Completed ~6 months following LPLV
CSSIL - ANS -Clinical Study Systems Implementation Leader
- Main contact on SMT for system setup questions/issues, IxRS activities, oversee all system
build timelines
CT ICSR - ANS -Clinical Trial Individual Case Study Report
CTA - ANS -Clinical Trial Application
CTM - ANS -Clinical Trial Monitor
ADaM - ANS -Analysis Data Model
- Analysis ready dataset, built from SDTM
AER - ANS -Adverse Event Report
AESI - ANS -Adverse Events of Special Interest
- Non-serious AEs which will be defined in the protocol for immediate reporting from investigator
to sponsor (within 24hrs of awareness), and are entered onto safety database
ALS - ANS -Architect Loader Spreadsheet
- Excel file
BAD - ANS -Biometrics Application Development
BAM - ANS -BioAnalytical Manager
BCE - ANS -Biometrics Computing Environment
BDL - ANS -Batch Data Loading
- Single push of data from one environment to another
BGPL - ANS -Biometrics Global Process Library
BOPM - ANS -Bioanalytical Operations Project Manager
BOR - ANS -Biosample Operations Responsible
BRIDG - ANS -Biometric Research Integrated Domain Group
BS - ANS -Biostatistics
BSO - ANS -Biometrics Strategic Operations
BV - ANS -Batch Validation
CASA - ANS -Clinical Application System Analyst
- System role withing Rave (CP)
CCDM - ANS -Clinical Coding & Dictionary Management
, CCS - ANS -Clinical Coding Specialist
CDASH - ANS -Clinical Data Acquisition Standards Harmonization
CDISC - ANS -Clinical Data Interchange Standards Consortium
CFDD - ANS -Custom Function Design Document
CFR - ANS -Code of Federal Regulation
CLT - ANS -Canadian Leadership Team
COLD - ANS -Collection Date
COREMAP - ANS -Corporate Records Management Programme
CP - ANS -Clinical Programmer
CPA - ANS -Clinical Programmer Analyst
cRMP - ANS -Core Risk Management Plan
CS - ANS -Clinician Scientist
CSIL - ANS -Clinical Study Implementation Leader
CSM - ANS -Country Study Manager
- Responsible for study performance within a single country
CSMS - ANS -Clinical Systems Management and Support
CSR - ANS -Clinical Study Report
- Summarizes all results from clinical study. Completed ~6 months following LPLV
CSSIL - ANS -Clinical Study Systems Implementation Leader
- Main contact on SMT for system setup questions/issues, IxRS activities, oversee all system
build timelines
CT ICSR - ANS -Clinical Trial Individual Case Study Report
CTA - ANS -Clinical Trial Application
CTM - ANS -Clinical Trial Monitor