Dictionary

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Dictionary entries are generally the label of a data field on a screen in CRMS. Because the same name can mean different things in different contexts, the screen name, in brackets, has been appended to the name if needed to remove ambiguity. That is, below, the entry

Status [Consent]

is a reference to the field labelled Status on the Consent screens. Some labels do have parentheses in them, so look closely.


A, B, C, D, E, F, G, H, I, J, K, L, M, N, O, P, Q, R, S, T, U, V, W, X, Y, Z


A
Accrual to Date [Site]
Accrual to Date (all sites)
Accrual to Date at Hopkins
Activation Date [Consent]
Activation Date [Protocol]
Activation Date [Site]
Additional Staff
Administrative Program Manager
Ancillary Protocol Number
Archive
Auditing
Authorized By
B
BMT
Blinded
Block this study from going to Epic
Budget Number
C
Checklist Status
Closed By
Closed to Accrual Date
Co-Investigator
Comment [Admin]
Consent
Consent Date
Consent Form
Consent Name
Consent Type
Consent Version Date
Consent Version Number
Consented By
Consentor
Contact Info
CRC Approval Date
CRC Required
CRMS Number
CRMS Status
Cross Referenced FDA Files
Current Screen Failures
D
Date Budget Expires
Date Consented
Date Contract Executed
Date Contract Sent to ORA
Date Entered[Regulatory Log]
Date Marked Candidate
Date Off Study
Date On Study
Date Site Closed
Date Started
Date Submitted [Regulatory Log]
Date to IRB [Regulatory Log]
Date Updated
Department
Department/Division
Display Name [Site]
Document Type [Regulatory Log]
Domain
E
eIRB Status
Email
Embedded Agreement
Embedded Agreement Description
Embedded Agreement Name
Embedded Agreement Type
Enrollment Definitions
Enrollment Status
Entered By
Entered By [Regulatory Log]
EPIC Payer Code
EPIC Payor Code
EPIC Study Name
Estimated Length of Study
Evaluable
External Contacts
External Monitor
F
FDA Department
FDA Logs
FDA Manager
FDA Reports
FDA Sponsor
Financial or Material Sponsor
G
General Clinical Research Center
GCRC
Gender
Gender (Protocol)
Grant Number
H
Has This Study Been Sent to Epic?
History Number
I
IDE
IDE Number
IDE Sponsor
IDE Holder
IDE Holder Type
IND
IND Number
IND Sponsor
IND Holder
IND Holder Type
IND/IDE Sponsor
IND/IDE Holder
Initial IRB Approval Date
Insurance Clearance Type
Internal Contacts
Interventional Study
Investigational/Administrative Study
IRB
IRB Approval Date [Consent]
IRB Approval Date [Regulatory Log]
IRB Approval Date [Site]
IRB Approval Number [Site]
IRB Expiration Date
IRB Number
IRB Expiration Date [Site]
IRB Termination Date
Is Hopkins the Coordinating Center for this study?
Is Hopkins the Coordinating Center for this study
Is this a cancer study?
Is this a cancer study
Is this a multi-site study?
Is this a multi-site study
J
JHMIRB Committee
Johns Hopkins Authored
Johns Hopkins Authored?
K
Keywords and Title
L
Last time patient Enrolled
Last Tx
Latest IRB Approval Date
Lead Study Coordinator
Lead Research Nurse
M
Max. Reimbursable Screen Failures
N
Name [Consent]
Name [Eligibility Checklist]
Name [Site]
NCI Code [Site]
NCT Category
NCT Code
New Consent [Consent]
New Consent [Patient]
New Trials
New Version
Number
Number of Sites
O
Off Study
Off Study Reason
Off Tx
Official Name [Site]
On Study Date
On Tx
Other Affiliated Group
Other Staff
P
Patient Site of Consent
Per Patient Fee
Phase
PI
PI [Site]
PI Affiliation
PI's Department/Division
Population
PRA Required
Principal Investigator
Projected Accrual
Projected Accrual (all sites)
Projected Accrual at Hopkins
Projected Annual Accrual (all sites)
Projected Annual Accrual at Hopkins
Projected Consents at Hopkins
Projected Years of Active Accrual
Protocol Comment
Protocol IRB Number
Protocol Number
Protocol Status
Protocol Title
Q
QA Specialist
R
RAC Review
Reason Closed
Reason for Override
Reason Off Study
Receipt No. [Regulatory Log]
Recipient [Regulatory Log]
Reconsent
Regulatory Log Date Entered
Regulatory Log Date to IRB
Regulatory Log Date Submitted
Regulatory Log Document Type
Regulatory Log Entered By
Regulatory Log IRB Approval Date
Regulatory Log Notes
Regulatory Log Receipt Number
Regulatory Log Recipient
Regulatory Log Submission Summary
Regulatory Log Submitted to
Regulatory Staff
Research Manager
Research Nurse
Research Program
S
SKCCC DSMP
Screen Failure
Screening Failure Fee
Search CRMS by History Number
Search CRMS by Name
Search EPR and CRMS by History Number
Secondary Program
Short Title
Site
Site Code
Site IRB Approval Number
Site IRB Expiration Date
Site [Patient]
Site Status for Study
Sponsor
Sponsor's Protocol Number
Start New Checklist
Statistician
Status
Status [Consent]
Status [IND/IDE]
Status [Protocol]
Status [Site]
Study Active in CRMS
Study Arms
Study Category
Study Code
Study Contact Role
Study Contacts
Study Coordinator
Study Site Id
Study Type
Subject Number
Subject Progress
Support Provided
Submission Summary [Regulatory Log]
Submitted to [Regulatory Log]
Therapeutic Study
T
Type [Consent]
Type [Eligibility Checklist]
Type [of Support Provided by Sponsor]
Type of Cancer
U
Update Checklist
V
Verified By [Eligibility Checklist]
Version Date [Consent]
W
X
Y
Z
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