SMARTSOLVE FUNDAMENTALS
Manage risk, eliminate variance, and facilitate compliance
Simplify the management of quality compliance for your small pharma business with IQVIA SmartSolve® Fundamentals.
Simplify the management of quality compliance for your small pharma business with IQVIA SmartSolve® Fundamentals.
Manage CAPAs and verify effectiveness
SmartSolve Fundamentals CAPA Management helps small pharma organizations to develop a risk-based, streamlined problem resolution process. It enables you to record a problem, establish and monitor corrective and preventive actions and review the effectiveness of each CAPA. By facilitating an effective CAPA process, SmartSolve Fundamentals CAPA Management can help you shorten cycle times, resolve issues quickly and prevent recurrence helping to ensure compliance with industry, quality, and regulatory requirements.
Securely store documents, manage revision control and route documents for review and approval
SmartSolve Fundamentals Document Management allows small pharma businesses to organize document lifecycles, accelerate reviews, and enforce document training. Users can read and sign off, prepare document profile, define training requirements and periodic reviews. The Document Management module follows a workflow with the following steps:
Capture, verify, and investigate product and process deviation
SmartSolve® Fundamentals Deviation Management is equipped with best-practice workflows to identify, mitigate, and reduce the risks associated with unexpected events in your manufacturing process.
Make informed decisions and implement changes quickly
SmartSolve Fundamentals Change Management provides you with the ability to define and assess change plans, implement individual action plan items, as well as review effectiveness for those changes that may be the result of a CAPA. It helps you to ensure consistent and compliant change control within your organization and your operations. SmartSolve Fundamentals Change Management gives your organization the tools to:
Learn how this powerful workflow-driven, pre-built solution can help you to manage risk, eliminate variance and facilitate compliance.
Identified as best in class North American QMS market for life sciences industry.
Connected, integrated, compliant. Build, scale, and optimize your quality and regulatory workflows with SmartSolve®, IQVIA's transformative Enterprise Quality Management System, built for Life Sciences.
From manufacturing oversight to regulatory requirements, manage quality across your organization with a single enterprise software solution.
Automate and standardize your regulatory management, from correspondence and commitments to registration and tracking.