BSI Quality Document Management System (BSI Quality DMS) serves as a centralized platform for efficiently creating, approving, and maintaining all documents critical to R&D including drug development, trial planning and execution, manufacturing, and regulatory compliance.
It ensures regulatory adherence by facilitating document version control, audit trails, secure storage, and retrieval, while also enabling seamless document creation and management processes through automated workflows and electronic signatures.
With features such as advanced search capabilities, easily customizable reports and integrations with other systems, BSI Quality DMS enhances overall efficiency in managing and overseeing the extensive documentation required in highly regulated industries.
- Enable collaboration - BSI Quality DMS fosters collaboration through facilitating seamless document creation, review, and approval processes.
- Improve compliance - BSI Quality DMS helps highly regulated industries ensure compliance by providing version controls, ensuring that only the latest approved documents are accessible.
- Easy access to documents - BSI Quality DMS offers intuitive search functionalities which enable locating necessary documents quickly by for example document type, geographical relevance, or keywords.
- Customizable reports and dashboards - BSI Quality DMS allows users to generate insightful reports on key metrics related to document management such as compliance status, document access history, and workflow performance.
- Audit and Inspection Readiness - A thorough audit trail and efficient search functionalities within BSI Quality DMS facilitate a smooth audit and inspection process.
