Integrated EQMS to Support the Manufacturing of High Quality, Safe and Effective Pharmaceutical Products
Title21 provides a comprehensive platform to enable holistic and integrated quality management processes through an intuitive interface to support the quality-related needs of pharmaceutical manufacturers. With Title21, pharmaceutical organizations can generate efficiencies, comply with regulatory standards and maintain a competitive edge.
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Increase Efficiency
Electronic workflows, collaboration tools, and automated approval routing helps you reduce time and costs while improving overall quality.
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Achieve Closed-Loop Quality Management
Title21’s solutions natively integrate on a common platform, enabling integrated processes and a single interface and database to manage all your compliance-driven data including document control, CAPA, audit and training.
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Streamline Document Control Processes
Simplify the revision and approval process of controlled policies, procedures and SOPs with Title21 Document Control, complete with periodic review, change control and read-and-sign training.
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Manage Staff Training
Ensure effective training management and a knowledgeable staff through competency checklists, quizzes and exams, and comprehensive training plans.
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Meet Regulatory Requirements
Title21 solutions support 21 CFR Part 11 including a full audit log, permission-based data access control, validation documentation and more.
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Generate CAPAs
Document all non-conformances, deviations and errors while ensuring timely resolution through risk assessment tools and the ability to launch a CAPA from your error form.
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Accelerate ROI
Title21 Best-in-Class Forms and Workflows are flexible, out-of-the box solutions that can be deployed quickly with minimal impact to your IT Operations. Title21 offers both HIPAA-compliant private cloud and on-premise installation options to support both small and multi-site firms.
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Track, Trend, and Report on Actionable Data
Perform trend analyses and run real-time reports on quality data throughout your operations to increase visibility of potential compliance risks and promote continuous quality improvement.
"We launched Title21 in January 2007 and it has made a huge impact in the way our QA group conducts business at Palatin Technologies. Installation had minimal interruption to our IT staff and integrated seamlessly with our current network. We are currently using the software to handle all deviations, change requests, CAPA's and document management including SOPs, specifications, protocols, reports, etc. Training was well received, users were pleased with how easy it is to access information and I was quite surprised how fast employees adjusted to the new system. The system is making everyone at Palatin more accountable with respect to quality; it is becoming a great tool for reporting metrics, and it is allowing us to focus on other areas of continuous improvement. Title21 was the solution we needed to assure Palatin maintains a high level of compliance."
Explore Title21's Integrated Solutions for Pharmaceutical Organizations
Title21's integrated quality management software provides paperless solutions for all your compliance-driven processes - all in one integrated platform.
