Kriya Integrations

Greenbox is an innovative document management system that combines a business process management system with a unique document management system. It is a Document Management System which allows for the storage, tracking, retrieval, and management of documents. Anybody with permission can access any file, regardless of where it is located. The system ensures complete confidentiality and safety of the documents and is designed for simplifying otherwise complex operations. Greenbox gives the user access to many features, including unlimited folders and subfolders and Solr OCR/text searching inside an image, document restoration, document versioning, granular access control, and advanced document control. Its most notable features include document approval workflow, intelligent handling of metadata, and an attractive pricing bracket.

Artwork is a simplified collaboration platform that allows you to manage artworks in the most efficient way. It reduces turnaround time and minimizes the chance of making mistakes. Artwork detects subtle differences that human eyes cannot see, resulting in error-free proofreading. It is Collaboration and Proofing tools. It uses checklists and annotation tools for collaboration and reducing rework. Artwork Management Software optimizes all aspects of the artwork process. Artwork Software provides the following features: Workflow configuration Reminders & escalations Auto-detection and detection of differences Tracking of comments by the on-screen proofreader Vendor & printer portal Version management and central artwork repository Reports and analysis Audit trail for all activities Artwork Approval Workflows Asset Library Reporting and Metrics

QMS allows companies to eliminate paper-based quality control processes while still adhering to regulatory standards and compliance. QMS not only improves operational efficiency, but also increases compliance to established quality standards. QMS combines all your quality processes into one place. It integrates related actions and processes to facilitate better analysis and process improvement. QMS has been vetted by the USFDA and European Regulatory Auditors and found to be compliant with CFR 21 Part 11 guidelines. Benefits All related processes can be managed from a single platform Reduce expensive mistakes Evidence to support educated decision making Credibility improvement Improved customer satisfaction