PRISYM ID has unveiled a specialized cloud-based labeling solution designed to meet the urgent demands of COVID-19 clinical trials. The PRISYM 360 SaaS platform offers pharmaceutical companies and research organizations immediate access to validated clinical label printing capabilities, addressing a critical component of accelerated trial processes.
The platform's pre-validated nature eliminates substantial validation costs and implementation delays typically associated with labeling systems deployment. This strategic advantage becomes particularly crucial as the life sciences sector races to conduct COVID-19 trials with unprecedented speed.
Advanced Technical Capabilities
The system incorporates comprehensive security measures and technical features essential for clinical trial operations. Key functionalities include:
- Role-based access controls for enhanced security
- Printer-agnostic label design capabilities
- Sequenced printing for clinical trial supply management
- Comprehensive audit logging with secure content transfer options
- Multi-language management systems
- Version control for all design elements and workflows
- Clinical trial data management with randomized data import capabilities
- GS1-compliant barcode support for clinical trials
Streamlined Implementation Process
The platform's cloud-based architecture minimizes technical barriers to entry, requiring minimal IT infrastructure investment while maintaining compliance with industry regulations. The pre-validated environment ensures immediate operational readiness, allowing organizations to focus on their core research objectives.
Warren Stacey, SVP of Sales at PRISYM ID, emphasizes the solution's strategic importance: "With the life science industry working at exceptional speed to run trials and accelerate the speed at which they come to market, labeling may be something of an afterthought. Yet it is critical to the process. Generic labeling software may be a blunt tool when it comes to validation, version control, compliance and navigating the nuances of the clinical trials supply chain."
Quality Assurance and Compliance
The platform maintains strict compliance with regulatory requirements through:
- Comprehensive audit trail capabilities
- Validated cloud environment
- Secure data management protocols
- Version control systems for all content and workflows
This systematic approach to compliance helps organizations maintain regulatory adherence while accelerating their clinical trial processes, particularly crucial in the context of COVID-19 research initiatives.
