Audience

Organizations that need a clinical trial management system

About OpenText Clinical Trial Quality Management

Over the last several years, the Life Sciences industry has faced nearly $15 billion in fines and compliance-related settlements, making it critical for companies to adhere to pharmaceutical, medical device and biotech best practices. Efficient and effective management of clinical trials can also significantly impact the time, scope and budget for the development of a drug or medical device. With OpenText™ Clinical Trial Quality Management System (ctQMS), companies can remain compliant, reduce costs of records management and establish best practice through collaboration before, during and after the clinical trial lifecycle.

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No integrations listed.

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Company Information

OpenText
Founded: 1991
Canada
www.opentext.com/info/clinical-trial-management

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Product Details

Platforms Supported
Cloud
Training
Documentation
Support
Phone Support
Online

OpenText Clinical Trial Quality Management Frequently Asked Questions

Q: What kinds of users and organization types does OpenText Clinical Trial Quality Management work with?
Q: What languages does OpenText Clinical Trial Quality Management support in their product?
Q: What kind of support options does OpenText Clinical Trial Quality Management offer?
Q: What type of training does OpenText Clinical Trial Quality Management provide?

OpenText Clinical Trial Quality Management Product Features

Clinical Trial Management

Monitoring Not Supported
21 CFR Part 11 Compliance Not Supported
Electronic Data Capture Not Supported
Enrollment Management Not Supported
Patient Database Not Supported
HIPAA Compliant Not Supported
Document Management Not Supported
Scheduling Not Supported
Recruiting Management Not Supported
Study Planning Not Supported

OpenText Clinical Trial Quality Management Additional Categories