Clinical Trial Software
19 products
RTSM
Prelude
·Clinical Trial Software
-
ePRO
Prelude
·Clinical Trial Software
-
Prelude EDC
Prelude
·Clinical Trial Software
-
Real World Evidence System
Okeiro
·Clinical Trial Software
-
Evidence Generation Hub
Resilience Care
·Clinical Trial Software
-
Veeva SafetyDocs
Veeva
·Clinical Trial Software
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Veeva Safety
Veeva
·Clinical Trial Software
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Veeva Safety Suite
Veeva
·Clinical Trial Software
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Veeva Submissions
Veeva
·Clinical Trial Software
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Veeva eCOA
Veeva
·Clinical Trial Software
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Veeva EDC
Veeva
·Clinical Trial Software
-
Veeva Disclosures
Veeva
·Clinical Trial Software
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Veeva Site Connect
Veeva
·Clinical Trial Software
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Veeva RTSM
Veeva
·Clinical Trial Software
-
Veeva Study Startup
Veeva
·Clinical Trial Software
-
Veeva CTMS
Veeva
·Clinical Trial Software
-
Veeva eTMF
Veeva
·Clinical Trial Software
-
Real-World Evidence Analytics Platform
Veradigm
·Clinical Trial Software
-
Inato Platform
Inato
·Clinical Trial Software
-
Clinical Trial SoftwareMain
A system to manage randomization and track trial supply seamlessly, tailored to specific protocols to keep clinical sites moving efficiently.
Features
- Manage randomization directly in the EDC
- Track treatment and placebo supply across sites in real time
- Automate restocking to avoid delays
- Monitor patient dispensing data as it happens
- Support various randomization methods including block, stratified, and adaptive
- Ensure data compliance with GCP and 21 CFR Part 11 standards
- Import IRT-managed randomization for complex designs
- Adapt to protocol amendments or unique trial requirements
Clinical Trial SoftwareMain
A system to manage randomization and track trial supply seamlessly, tailored to specific protocols to keep clinical sites moving efficiently.
Features
- Manage randomization directly in the EDC
- Track treatment and placebo supply across sites in real time
- Automate restocking to avoid delays
- Monitor patient dispensing data as it happens
- Support various randomization methods including block, stratified, and adaptive
- Ensure data compliance with GCP and 21 CFR Part 11 standards
- Import IRT-managed randomization for complex designs
- Adapt to protocol amendments or unique trial requirements