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Description

Citeline serves as a robust platform for clinical development intelligence and analytics, offering life sciences organizations access to real-time research and development data, insights, and tools essential for making informed strategic choices throughout the drug and device development process. By compiling and refining the most comprehensive datasets related to global clinical trials, investigators, trial sites, drug development pipelines, and regulatory stipulations, it aids various functions including protocol design, feasibility assessments, selection of sites and investigators, enrollment predictions, competitive analysis, and tracking compliance with disclosure regulations in different jurisdictions. The platform encompasses several products, such as Pharmaprojects for monitoring drug pipelines, Trialtrove for benchmarking clinical trials, Sitetrove for gathering site and investigator intelligence, Global Patient Insights for ensuring feasibility aligns with actual patient access, and TrialScope Intelligence/Disclose for navigating regulatory disclosure requirements. With its wide range of functionalities, Citeline stands out as a vital resource for organizations aiming to streamline their clinical development processes and enhance their strategic decision-making capabilities. Moreover, the integration of these tools facilitates a more efficient approach to managing the complexities of clinical trials and regulatory compliance in an ever-evolving landscape.

Description

In recent years, the Life Sciences sector has incurred nearly $15 billion in fines and settlements related to compliance, underscoring the importance for firms to follow best practices in pharmaceuticals, medical devices, and biotechnology. Additionally, the way clinical trials are managed can greatly influence the timeline, scope, and financial resources allocated for the development of drugs or medical devices. Utilizing OpenText™ Clinical Trial Quality Management System (ctQMS) allows organizations to maintain compliance, lower record management expenses, and foster collaboration to implement best practices throughout the entire clinical trial lifecycle. This strategic approach not only enhances operational efficiency but also contributes to the overall success of product development initiatives.

API Access

Has API No 

API Access

Has API No 

Screenshots View All

Screenshots View All

No images available

Integrations

No details available.

Integrations

No details available.

Pricing Details

No price information available.
Free Trial No 
Free Version No 

Pricing Details

No price information available.
Free Trial No 
Free Version No 

Deployment

Web-Based Yes 
On-Premises No 
iPhone App No 
iPad App No 
Android App No 
Windows No 
Mac No 
Linux No 
Chromebook No 

Deployment

Web-Based Yes 
On-Premises No 
iPhone App No 
iPad App No 
Android App No 
Windows No 
Mac No 
Linux No 
Chromebook No 

Customer Support

Business Hours Yes 
Live Rep (24/7) Yes 
Online Support Yes 

Customer Support

Business Hours Yes 
Live Rep (24/7) No 
Online Support Yes 

Types of Training

Training Docs Yes 
Webinars Yes 
Live Training (Online) Yes 
In Person No 

Types of Training

Training Docs Yes 
Webinars No 
Live Training (Online) No 
In Person No 

Vendor Details

Company Name

Citeline

Country

United States

Website

www.citeline.com

Vendor Details

Company Name

OpenText

Founded

1991

Country

Canada

Website

www.opentext.com/info/clinical-trial-management

Product Features

Product Features

Clinical Trial Management

21 CFR Part 11 Compliance No 
Document Management No 
Electronic Data Capture No 
Enrollment Management No 
HIPAA Compliant No 
Monitoring No 
Patient Database No 
Recruiting Management No 
Scheduling No 
Study Planning No 

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