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What is Trialpack Designer II?
The Trialpack Designer is an intuitive yet powerful software application tailored for the creation of blister packs and cards intended for clinical trials. It is particularly adept at designing packaging for complex blinded studies, such as those involving dosage titrations, double-dummy configurations, and cross-over trials, where a single package might include multiple items. The application effortlessly supplies essential configuration data for the Trialpack PC Controller, Controlled Dosing Systems, and Robotic Packaging Systems. Users can conveniently create various blister shapes, print images, and filling patterns directly from the interface. Moreover, it incorporates detailed user access controls, streamlines workflows with electronic signatures, and maintains a thorough audit trail in adherence to 21 CFR Part 11 regulations. The system also produces reports that offer comprehensive packaging instructions alongside a detailed inventory of material needs, which ensures meticulous documentation and compliance for trial activities. This versatile tool plays a vital role in preserving the integrity and organization of clinical trial packaging, ultimately contributing to the success of the trials conducted. Furthermore, its user-friendly design makes it accessible for professionals at all levels, enhancing collaboration and efficiency throughout the research process.
What is GRAVITY?
In the field of clinical research, meticulous organization is crucial for achieving effective outcomes. The challenge of deploying the right resources at the right time becomes particularly pronounced when it comes to managing documents during a clinical trial. GRAVITY has emerged as a trusted solution for overseeing site files and trial master files. We have reimagined these documents into an accessible and unified electronic format, which significantly improves document management by offering a structured and practical system. Acting as an integrated eTMF and eISF platform, GRAVITY functions as a comprehensive cloud-based Document Management System (DMS), serving as a central hub for sponsors, contract research organizations (CROs), and research sites. Additionally, GRAVITY can be utilized independently by each stakeholder when required. As soon as a site is selected for a clinical trial, there is a surge of incoming documents that need to be managed with precision. GRAVITY incorporates a unique feature that tracks vital document management while alerting users to any documents approaching their expiration dates, thereby promoting compliance and operational efficiency throughout the trial. This forward-thinking strategy not only simplifies processes but also significantly elevates the overall quality of clinical research initiatives. Ultimately, GRAVITY stands as a testament to the advancements in document management technology within the clinical research landscape.
Integrations Supported
Additional information not provided
Integrations Supported
Additional information not provided
API Availability
Has API
API Availability
Has API
Pricing Information
Pricing not provided.
Free Trial Offered?
Free Version
Pricing Information
Pricing not provided.
Free Trial Offered?
Free Version
Supported Platforms
SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux
Supported Platforms
SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux
Customer Service / Support
Standard Support
24 Hour Support
Web-Based Support
Customer Service / Support
Standard Support
24 Hour Support
Web-Based Support
Training Options
Documentation Hub
Webinars
Online Training
On-Site Training
Training Options
Documentation Hub
Webinars
Online Training
On-Site Training
Company Facts
Organization Name
Fleximation
Date Founded
1994
Company Location
Switzerland
Company Website
www.fleximation.com/trialpack/designer/index.html
Company Facts
Organization Name
ASSAY Clinical Research
Date Founded
2012
Company Location
United Kingdom
Company Website
www.assaycr.com/gravity.php
Categories and Features
Clinical Trial Management
21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning
Categories and Features
Clinical Trial Management
21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning