Quality Management System by NextDocs
- 2. A Collaborative Quality Management Platform that Provides Transparency and Insight Across the Enterprise In recent years, the ICH, FDA and other regulatory authorities have re- established their positions on quality management systems to stress the A Recent FDA presentation on importance of product quality monitoring, corrective and preventative action Inspections and Findings states (CAPA), change control, and management review of quality performance. that 29% of 483s and 84% of Warning Letters contain references Many companies are poorly equipped to meet these challenges due to a lack of truly closed-loop process models and an inability to collaborate and to CAPA Deficiencies pass information between and among the full set of stakeholders including corporate management, quality assurance, and employees responsible for any quality-related job function. The NextDocs Solution Key Features and Benefits Our pre configured solutions for managing deviations, complains, audit All the benefits of a findings, change control and CAPA addresses these key challenges to traditional document deliver a compliant, user-friendly solution while minimizing the demands on management system and your already overtaxed business and IT Users. more: ● SOPs: An integrated solution that connects the entire SOP lifecycle » Support for and enforcement from creation through distribution and beyond. of your business processes ● CAPA: A comprehensive solution for managing Corrective and » Decreased time to review and Preventative Actions used in continuous improvement in quality and approve documents processes. » Significantly decreased ● Deviations: A fully configurable and automated solution to manage handling of paper Deviations and OOS from occurrence to investigation and closure. » 21 CFR Part 11 compliance ● Complaints: A full featured solution to manage recording, routing, and resolution of all customer complaints. » Streamlined validation, assisted by our validation ● Audit: Provides complete tracking of observations, findings, and toolkit recommendations. » Streamlined deployment and ● Change Control: A solution for controlling changes or modifications to increased user acceptance products and processes together with the management of associated due to our familiar user tasks. interface » Ability to provide user interface in the local language A FAMILIAR INTERFACE » Decreased cost of ownership Because NextDocs is built upon SharePoint, a technology that many and accelerated return on business users already use, training and ramp-up time are reduced. Most investment companies already have the ability to support and administer SharePoint – unlike highly specialized document management technologies where several administrators must sometimes be hired just to support a single application.
- 3. A CLOSED LOOP SYSTEM Many audit and inspection findings are related to deviations, complaints and The NextDocs Quality Management CAPAs not being tracked to closure. NextDocs offers form-based workflows System is one of our four platforms that provide Life Science companies that respond dynamically to decision factors such as the need for specific with best-of-breed solutions in investigations, escalations, or approvals. Processes are automatically tracked to document and quality management closure. Tight integration with email ensures that users are alerted to assigned, due and overdue tasks in the system they use all day – email. In addition, NextDocs views provide transparency and insight by highlighting incomplete or overdue processes and exposing overall trends. A COLLABORATIVE PROCESS Quality issue investigation and resolution normally rely upon collaboration. Because NextDocs is built on SharePoint, the industry-leading collaboration platform, all of the tools needed for true collaboration are available out of the box. BUILT-IN COMPLIANCE NextDocs supports GxP and Part 11 compliance through the use of built-in and NextDocs Solutions configurable business processes for electronic review, approval and closure. Electronic signatures are required at any stages of the process that you specify. Quality Clinical Regulatory Corporate SCALABLE FOR THE ENTERPRISE NextDocs Compliance Platform SharePoint has the proven ability to manage millions of documents over local and wide area networks, providing users with the performance they expect. By using Microsoft SharePoint SharePoint, you eliminate the need to implement complicated IT solutions if you expand to a new region or office. Quality Management Solution Components When you purchase a NextDocs Quality Management System solution, you start with a product that is fully configured for use in managing QMS processes, and which could be validated and deployed by doing nothing more than adding specific information about your products, departments, etc. to pre-existing lists, and adding your users to appropriate roles. STANDARD SOLUTION COMPONENTS » Preconfigured QMS Processes for one or more of the following: » Predefined lists that limit valid values for document properties to values that you supply » Forms to gather the data required in your QMS processes » Dynamic review and approval workflows that dynamically adjust processes as content is added to forms » Views for tracking overall process status » Role-based security » Electronic signature » Audit trail » 21 CFR Part 11 Compliance
- 4. NEXTDOCS COMPLIANCE PLATFORM The NextDocs Compliance Platform includes a comprehensive set of features that addresses all ICH, FDA, EMEA, and MHLW regulatory requirements. It is built in and fully integrated with the Microsoft SharePoint Server framework. â– Real-time Adobe PDF conversion triggered by â– Version tracking with major and minor versioning, version document state change or workflow step history and previous version restoration â– Controlled document management including â– Configurable document numbering configurable application of watermarks & overlays â– Auto population of document properties â– Full lifecycle management of the document from inception to obsolescence â– Electronic/digital signatures that address all regulatory requirements â– Flexible and powerful process automation tools for change requests, document review, and approval â– Audit trails that provide a detailed log of every activity performed in the system â– Check in/Check out controls to prevent documents from being overwritten NextDocs is the global leader in providing Microsoft SharePoint-based document and Main Headquarters EU Headquarters quality management solutions to life sciences organizations. It enables businesses in 500 N. Gulph Road Elisabethstrasse 91, regulated industries to achieve compliance with FDA and other agencies while automating Suite 240 80797 Munich processes, improving efficiency and dramatically reducing costs. NextDocs customers King of Prussia, PA 19406 Germany include Pharmaceutical companies, Bio-Techs, Medical Device companies and CROs. Tel: 610.265.9474 Tel: +49.89.5908.1435 For more Information visit www.nextdocs.com Accredited by ANAB