ID

24371

Descripción

Study part: Investigator’s Signature End of Study.An Open-Label Extension phase 3 Study with REQUIP (ropinirole) CR for Subjects from Studies 101468/165, 101468/168 and 101468/169 Patient Level Data. Study ID:101468/248, Clinical Study ID: 101468/248.

Palabras clave

  1. 30/7/17 30/7/17 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

30 de julio de 2017

DOI

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Licencia

Creative Commons BY-NC 3.0

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Investigator’s Signature End of Study Ropinirole NCT00632736

Investigator’s Signature End of Study

INVESTIGATOR’S SIGNATURE
Descripción

INVESTIGATOR’S SIGNATURE

Alias
UMLS CUI-1
C2346576
Subject ID
Descripción

Subject ID

Tipo de datos

text

Alias
UMLS CUI [1]
C2348585
I confirm that I have reviewed the data in this Case Report Form for this subject. All information entered by myself or my colleagues is, to the best of my knowledge, complete and accurate, as of the date below.
Descripción

consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1511481
Investigator’s Signature :
Descripción

Investigators signature

Tipo de datos

text

Alias
UMLS CUI [1]
C2346576
Investigator’s name
Descripción

Investigator name

Tipo de datos

text

Alias
UMLS CUI [1]
C2826892
Date
Descripción

Date

Tipo de datos

date

Alias
UMLS CUI [1]
C0011008

Similar models

Investigator’s Signature End of Study

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
INVESTIGATOR’S SIGNATURE
C2346576 (UMLS CUI-1)
Subject ID
Item
Subject ID
text
C2348585 (UMLS CUI [1])
consent
Item
I confirm that I have reviewed the data in this Case Report Form for this subject. All information entered by myself or my colleagues is, to the best of my knowledge, complete and accurate, as of the date below.
boolean
C1511481 (UMLS CUI [1])
Investigators signature
Item
Investigator’s Signature :
text
C2346576 (UMLS CUI [1])
Investigator name
Item
Investigator’s name
text
C2826892 (UMLS CUI [1])
Date
Item
Date
date
C0011008 (UMLS CUI [1])

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