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.
Electronic workflows, collaboration tools, and automated approval routing helps you reduce time and costs while improving overall quality.
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.
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.
Ensure effective training management and a knowledgeable staff through competency checklists, quizzes and exams, and comprehensive training plans.
Title21 solutions support 21 CFR Part 11 including a full audit log, permission-based data access control, validation documentation and more.
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.
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.
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.
Quality Assurance Compliance Manager
Palatin Technologies, Inc
Title21's integrated quality management software provides paperless solutions for all your compliance-driven processes - all in one integrated platform.