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1
Select the tool(s) you would like to configure:
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Clinical Trial Management System
Electronic Data Capture
Electronic patient-reported outcome
Randomization and Trial Supply Management
Electronic informed consent
Ethical Review Mangement System
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2
Enter the number of trials/projects:
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for the upcoming 12 months
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3
Indicate the type of trial(s)/project(s) involved:
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Single center
Multicenter
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4
Select your required CTMS element(s):
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Submission management (Registration forms, eTMF/ISF, Assessment)
Amendments, SAE/SUSAR & Report Management
Financial Management (Manage budgets, expenses, and reimbursements)
Clinical Subject Management (Schedule & monitor patient visits)
Integrated Study Communications (e.g. with Team Members)
Trial Dashboards
API
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5
Which industry describes as best your organization?
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Healthcare
CRO
Pharma/BioTech
Academic institutions
Medical Devices
ECs/IRBs
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6
Your contact information
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First Name
Last Name
Name of institution or company
Please enter your email
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