+
+

Related Products

  • Lockbox LIMS
    72 Ratings
    Visit Website
  • QBench
    152 Ratings
    Visit Website
  • AdvancedMD
    2 Ratings
    Visit Website
  • Sumsub
    227 Ratings
    Visit Website
  • RegDesk
    19 Ratings
    Visit Website
  • TraceEngine
    1 Rating
    Visit Website
  • Sovos
    158 Ratings
    Visit Website
  • Polonious
    2 Ratings
    Visit Website
  • Ethena
    131 Ratings
    Visit Website
  • ManageEngine Log360
    190 Ratings
    Visit Website

About

Citeline is a clinical development intelligence and analytics platform that provides real-time R&D data, insights, and tools to life sciences organizations to inform strategic decisions across the drug and device development life cycle. It aggregates and curates the world’s most extensive datasets on global clinical trials, investigators, trial sites, drug development pipelines, and regulatory requirements, supporting functions such as protocol design, feasibility analysis, site and investigator selection, enrollment forecasting, competitive benchmarking, and compliance tracking with disclosure obligations across jurisdictions. It includes products like Pharmaprojects for pipeline monitoring, Trialtrove for clinical trial benchmarking, Sitetrove for site/investigator intelligence, Global Patient Insights for aligning feasibility with real patient access, and TrialScope Intelligence/Disclose for managing regulatory disclosure requirements.

About

RegDocs Connect gives your operational and regulatory teams the tools they need to prepare complete and compliant submission ready documents and records. Built with the end user in mind, collaboration, automation and quality are the foundation of this solution. Automated workflows manage your records lifecycle from draft to final, enabling your team to be in complete control of your regulatory documents at all times. Mapping of document types to the EDM reference model and eCTD facilitates organization and retrieval of documents for inclusion in regulatory submissions. Proprietary tools such as PDF/A Publishing, document classification, and unique document identifiers provide a powerful regulatory document management solution that pulls information from across your organization, into one manageable solution. With the rise of electronic submissions to regulatory agencies and the increased complexity of drug development, the ability to produce submission-ready, quality content

Platforms Supported

Windows
Mac
Linux
Cloud
On-Premises
iPhone
iPad
Android
Chromebook

Platforms Supported

Windows
Mac
Linux
Cloud
On-Premises
iPhone
iPad
Android
Chromebook

Audience

Pharmaceutical, biotech, and clinical research professionals interested in a tool to plan, execute, and optimize drug development and clinical trial strategies

Audience

Operational and regulatory teams looking for a toolkit to prepare complete and compliant submission ready documents and records

Support

Phone Support
24/7 Live Support
Online

Support

Phone Support
24/7 Live Support
Online

API

Offers API

API

Offers API

Screenshots and Videos

Screenshots and Videos

Pricing

No information available.
Free Version
Free Trial

Pricing

No information available.
Free Version
Free Trial

Reviews/Ratings

Overall 0.0 / 5
ease 0.0 / 5
features 0.0 / 5
design 0.0 / 5
support 0.0 / 5

This software hasn't been reviewed yet. Be the first to provide a review:

Review this Software

Reviews/Ratings

Overall 0.0 / 5
ease 0.0 / 5
features 0.0 / 5
design 0.0 / 5
support 0.0 / 5

This software hasn't been reviewed yet. Be the first to provide a review:

Review this Software

Training

Documentation
Webinars
Live Online
In Person

Training

Documentation
Webinars
Live Online
In Person

Company Information

Citeline
United States
www.citeline.com

Company Information

Montrium
Canada
www.montrium.com

Alternatives

Alternatives

Medidata

Medidata

Dassault Systèmes
LifeSphere RIMS

LifeSphere RIMS

ArisGlobal
Biorce Aika

Biorce Aika

Biorce
KnowledgeNET

KnowledgeNET

Sarjen Systems
adWATCH

adWATCH

Atlant Systems
GlobalSubmit

GlobalSubmit

Certara

Categories

Categories

Document Management Features

Access Controls
Archiving & Retention
Collaboration Tools
Compliance Tracking
Document Archiving
Document Assembly
Document Capture
Document Conversion
Document Delivery
Document Indexing
Document Retention
Electronic Signature
Email Management
File Recovery
File Type Conversion
Forms Management
Full Text Search
Offline Access
Optical Character Recognition
Print Management
Version Control

Integrations

Montrium Connect

Integrations

Montrium Connect
Claim Citeline and update features and information
Claim Citeline and update features and information
Claim RegDocs Connect and update features and information
Claim RegDocs Connect and update features and information