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Description
Advanced clinical data analytics is essential for expediting and minimizing risks associated with regulatory approvals, thanks to our innovative automated analytics and validation platform. Unlike any other clinical data analytics software, our solution enhances data integrity and reduces the risks tied to submissions. By automating manual quality processes, you can avoid the hassle of QC reruns, eliminate instances of data duplication and inconsistencies, and maintain robust data traceability, all while ensuring a transparent quality assurance process. This leads to a faster time to market, allowing businesses to generate revenue sooner and reduce validation times effectively. Moreover, this efficiency frees up valuable resources and cuts costs, thereby accelerating the journey to regulatory approval. The demand for precise clinical data validation and top-tier data output is increasingly critical in today’s fast-paced environment. Verify is dedicated to managing and analyzing clinical data to minimize risk and hasten the approval process for new drugs and vaccines, ensuring that quality, speed, and success are at the forefront of your clinical trials. Ultimately, our platform empowers organizations to respond swiftly to market needs while maintaining high standards of compliance.
Description
Regardless of whether you are a seasoned professional or a newcomer to the regulatory submission landscape, the possibility of your electronic common technical document (eCTD) submissions being rejected is a significant concern, particularly in light of the increasingly intricate and evolving regulatory landscape. Furthermore, variations in eCTD submission requirements across different regions, along with the challenges of managing the entire document lifecycle, can complicate efforts to achieve your organization’s objectives for speeding up market release. By utilizing Certara’s GlobalSubmit™ eCTD submissions management software, your regulatory team will be equipped with the necessary tools to efficiently publish, validate, and review eCTD submissions. This approach allows you to mitigate risks and sidestep unnecessary complexities through a streamlined eCTD submission process, ultimately supporting your regulatory team as they strive to meet critical deadlines and bring treatments to patients. Therefore, as your regulatory department works diligently to meet tight timelines and ensure timely patient access to new therapies, filing your eCTD submissions becomes an essential task. Ensure that you have the right resources in place to enhance your submission efficiency, thereby bolstering your chances for success.
API Access
Has API
API Access
Has API
Integrations
No details available.
Integrations
No details available.
Pricing Details
No price information available.
Free Trial
Free Version
Pricing Details
No price information available.
Free Trial
Free Version
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Vendor Details
Company Name
Beaconcure
Founded
2016
Country
Israel
Website
beaconcure.com
Vendor Details
Company Name
Certara
Founded
2008
Country
United States
Website
www.certara.com/regulatory-science/globalsubmit-ectd-submissions-software/
Product Features
Text Mining
Boolean Queries
Document Filtering
Graphical Data Presentation
Language Detection
Predictive Modeling
Sentiment Analysis
Summarization
Tagging
Taxonomy Classification
Text Analysis
Topic Clustering