streamline clinical trial disclosure

CTD Planning & Tracking

Resource Forecasting

Automated Data Imports

80 Registration Templates

20 Results Templates

Milestone Management

Compliance Dashboards

User & Resource Training

"this system helps ensure our process and data is consistent, and completed on time"

registration & results


The CTD PUBLISHER is guaranteed to streamline and simplify your global Clinical Data Disclosure (CTD). This web-based system is designed to standardize your process and data while reducing the efforts required by expensive resources. CTD PUBLISHER automatically imports data from excel spreadsheets, internal systems and or public websites and shares common data across the structured forms. The configurable workflows, with email notifications, ensure the work is completed on time and captures all stakeholder actions. Just push a button to upload to clinicaltrials.gov and to your CTD REGISTRY. Although the CTD REGISTRY generates an approved file, the new EU portal does not currently allow for automatic uploads.

Sylogent, the creator of the CTD PUBLISHER, has more than ten years of experience with protocol registration and results disclosure and is available to assist with regulation tracking and process improvements.

The CTD PUBLISHER can be deployed and ready to use within days. The system includes an integrated training module that assists with user on-boarding. The migration utility instantly downloads sponsor records from clinicaltrials.gov and EudraCT. The unique system configuration enables users to modify records quickly and get them approved for publishing.

Study Master Form

US & EU Protocols Registration

US & EU Results Reporting

100 Integrated Templates

Locations Data Manager

ClinicalTrial.gov Auto Publish

EudraCT Approved XMLs

Milestone-Driven Workflows

Task Notification Alerts

Global Regulation Tracker


integrated with CTD REGISTRY

see it today

yes, it's that good!


Thank you!

We will get in touch shortly.

LEVEL 1

BASIC

15 Users

US Protocol & US Results Forms

EU Protocol & EU Protocol Forms

Basic Study Master Data

Planning & Tracking

US Result to EU Result Auto Author

Automated Workflow Notifications

Clinicaltrials.gov Auto Publish

Clinicaltrials.gov Comments Import

Clinicaltrials.gov NCTID Auto Import

Basic Reports & Dashboards

$50,000

YES
X

LEVEL 2

BUSINESS

50 Users

US Protocol & US Results

EU Protocol & EU Protocol

Study Master Form

Budgeting, Planning & Tracking

80 Registration Templates

20 Results Templates

US Result to EU Result Auto Author

Automated Workflow Notifications

Clinicaltrials.gov Auto Publish

Clinicaltrials.gov Comments Import

Clinicaltrials.gov NCTID Auto Import

Basic Reports & Dashboards

$100,000

YES
X

LEVEL 3

CORPORATE

250 Users

US Protocol & US Results

EU Protocol & EU Protocol

Study Master Form

Budgeting, Planning & Tracking

80 Registration Templates

20 Results Templates

US Result to EU Result Auto Author

Automated Workflow Notifications

Configurable Rules Scoping ( max automation )

Clinicaltrials.gov Auto Publish

Clinicaltrials.gov Comments Import

Clinicaltrials.gov NCTID Auto Import

Customized Reports & Dashboards


* includes 30% off CTD REGISTRY, PUBSTRAT and other products.

$250,000

YES
X

LEVEL 4

ENTERPRISE

Unlimited Users

US Protocol & US Results

EU Protocol & EU Protocol

Study Master Form

Budgeting, Planning & Tracking

Resource Forecasting

Compliance Milestone Management

80 Registration Templates

20 Results Templates

US Result to EU Result Auto Author

Automated Workflow Notifications

Customized Rules Scoping ( max automation )

Clinicaltrials.gov Auto Publish

Clinicaltrials.gov Comments Import

Clinicaltrials.gov NCTID Auto Import

Customized Reports & Dashboards


* includes 50% off CTD REGISTRY, PUBSTRAT and other products.

Contact

YES
X

"critical & affordable"

for all Pharmaceutical, Biotech & Device companies

a sylogent product

COMPLIANCE IN MOTION

Sylogent develops software that maximizes regulatory compliance, reduces operational costs and optimizes resource value. We leverage an integrated knowledge of process, data, technology and people to design solutions that deliver measurable results.

Compliance Tracking

Process Management

Enterprise Task Planning

Budgeting & Forecasting

Workflow Automation

Structured Data Management

Interactive Electronic Forms

Alerts & Notifications

trusted resource

Since 2002, Sylogent software has been utilized by pharmaceutical, biotech and medical device companies.

see it today

yes, it's that good!


Thank you!

We will get in touch shortly.