TrackWise Digital Document Control Software January 1, 2021 TrackWise Digital document control software keeps all your documents in a single, centralized location, helping you combine quality processes and more easily achieve regulatory compliance. Access and manage documents from any web-enabled device to improve visibility, collaboration, and efficiency throughout your operation in a controlled digital environment. Benefits of TrackWise Digital Document Control Software TrackWise Digital document management software provides an intuitive and collaborative environment for creating and managing controlled and uncontrolled documents. The easy-to-use system allows internal and external users to access, edit, store, and share quality content from any device with access to a web browser. TrackWise Digital document management software is fully integrated with other quality and regulatory solutions, enabling users to cross-reference records, such as which CAPAs and change controls require updated SOPs, and which users are trained on the updated documentation. Make employees more efficient Automate document routing, reviews, and notifications using a secure and accessible repository. Process rule-based, custom-configured, and automated workflows to meet your requirements. Improve collaboration View active documents directly in the dashboard. Authors, reviewers, and approvers can see which documents are in the review and approval process, and make comments, annotations, and edits in real-time within a web browser using Office 365. Connect processes Connect all aspects of your quality solution with your document and training repository. Users can seamlessly link documents to quality records and initiate revisions while content moderators can analyze trends and see which documents are linked to additional quality events. The system can automatically create new training records whenever a significant change is made. Implement a single source of truth Enable users to access, edit, store, and share quality content from a centralized repository, ensuring teams throughout the value chain use the latest versions of content. Be audit-ready TrackWise Digital’s audit trail and adherence to 21 CFR Part 11 tracks changes and actions so auditors can quickly find answers to their questions. Benefit From cloud-based resources Access and use every aspect of the system without installing any software. The entire system can be conveniently accessed through your web browser. Ensure regulatory compliance The software is fully compliant with 21 CFR Part 11, including a full audit trail and electronic signature functionality. You can always be sure that everyone is working off a single version of the truth. Features of TrackWise Digital Documentation Management Software Best-practice industry templatesTrackWise Digital’s best-practice templates enable quick implementation and support automated validation through software updates, minimizing IT burdens, lowering costs, and accelerating time to value. Out-of-the-box complianceTrackWise Digital is built around compliance with control over processes and information, enforced compliance with internal and external requirements, and 21 CFR Part 11 compliance, which includes electronic signature and audit trail features. Centralized system of recordManaging all quality processes on a single, centralized system streamlines cross-functional quality processes and enables robust reporting and analytics capabilities. The easy-to-use platform includes automated configurable workflows, productivity tools like tasks and alerts, reports, and dashboards. Salesforce platformBuilt on the trusted Salesforce platform, TrackWise Digital documentation management software leverages Salesforce’s security, stability, and native features such as form builder, reporting, process builder, Chatter, Salesforce1 Mobile App, integration, programmability, and access control. Resources About Document Management Solutions: WHITE PAPER: An Integrated Approach to Quality – How to Tighten the Connection between Quality Management and Document Management. DATASHEET: TrackWise Digital Document Management – Manage Quality Documents from Anywhere. BLOG: 3 Reasons to Take Your Document Management Digital – How does your organization manage important documents like policies and specifications? If you thought of a person or envisioned a gigantic three-ring binder, it’s time to upgrade your document management approach. BLOG: Removing Silos: The Value of an Integrated Quality and Document Management System (DMS) – Let’s consider why effective quality programs integrate quality management and document control processes to maximize the effectiveness of both solutions, increase visibility and create stronger collaboration. LEARNING: Course: TrackWise Digital Document Management System – This eLearning OnDemand course is for those new to the TrackWise Digital Document Management System (DMS) application. The course provides an overview of DMS as a document management tool. Top Industries for Electronic Document Management Software Each industry is different in terms of regulatory requirements, the needs of their customers, and manufacturing challenges. The flexibility of TrackWise Digital document control software allows it to be integrated into a vast range of industries and businesses to help increase efficiency. Pharmaceutical and Biotechnology Medical Device Manufacturing Food and Beverage Consumer Products Other Modules in Sparta’s TrackWise Digital QMS TrackWise Digital QMS software is an industry-leading quality and change control management system with integrated modules that work together to support quality, compliance, and more efficient decision-making. Eliminate unnecessary papers, faxes, emails, and phone calls from your operation and manage all these processes and more through a single integrated platform. Complaint Management CAPA Supplier Quality Change Control Audit Management Quality Events Out of Specification Nonconformance Share via: Twitter LinkedIn Facebook Email
EVENT 9th GCC Regulatory Affairs Pharma Summit (and Quality Conference) 2024 GCC Regulatory Affairs Pharma Summit is an annual event that provides platform for pharmaceutical regulatory experts and industry professionals in the GCC region to share insights and discuss about the latest updates in the pharmaceutical regulations. We are Gold Sponsors of the 9th GCC Regulatory Affairs Pharma Summit 2024. Learn more
EVENT 7th Annual European Medical Device QA & SQM Conference 2024 The 7th Annual European Medical Device and Diagnostic Supplier Quality Management Conference aims to bring together the industry’s top-performing Supplier Quality Management (SQM) & QA QC professionals under one roof. We are Bronze Sponsors of the 2024 Medical Device QA & SQM Conference in Belgium. Learn more
EVENT TUG Americas Join industry peers at one of these FREE events for TrackWise and TrackWise Digital customers, with two dates and locations to choose from. Learn more
EVENT Building a Winning Life Science Eco-system – Leveraging the Quality Link between Platform, Processes and Patients Watch this unique webinar to discover how Life Science organizations can a combine a best-in-class platform with freedom of solution choice to improve product quality, productivity, and supply chain continuity. Learn more
CASE STUDY Empowering Innovation: Revelle Aesthetics Transforms Document Management and Training with TrackWise Digital Revelle Aesthetics selected TrackWise Digital to manage its key quality management processes—document management and training management. Learn more
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WEBINAR Meeting Compliance and Improving Efficiency with an integrated Quality Management System Join quality experts as they discuss how an integrated QMS can help manufacturers meet compliance while improving efficiency. Learn more
EVENT Quality Systems in the Digital Era: Are You Ready for the Future? Explore how to prepare for the future of quality systems in the digital era with Fabrizio Maniglio, Industry & Business Development Director. Hosted by Quality Digest. Learn more
BLOG The Power of Integration: A Holistic Approach to Quality and Document Management One of the key components for Life Sciences companies is to have their documents and data in order.... Learn more
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