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Product Description

EDI and MFT Integration Platform

Product Description

Prism is a fully integrated clinical trial management and EDC product that provides both standard data management functionality and value-added tools for clinical trial management. Prism combines ease-of-use with innovative features to provide a fresh solution for the collection and management of clinical trial data.

Product Description

XEDI is an EDI platform designed to connect customers with suppliers to process orders, invoices and other transactions.

Product Description

EdiFabric empowers developers and businesses interested in enabling their software systems with EDI capabilities. Its simplicity and effectiveness lets you connect with partners in just a day. Supports all versions for X12, HIPAA, EDIFACT, EANCOM and VDA. Fully customizable EDI rules for each transaction set, allowing you to comply with any partner-proprietary format.

Product Description

Comprehensive SAS based clinical data management, EDC, and clinical trials reporting system

Product Description

Suite of modules that assist in clinical trials through data input, management, consent forms, and electronic data capture forms.

Product Description

Order2Cash is an only end-to-end platform solution for credit scoring, online contract and document signing, e-invoicing, payment processing, credit management and document warehousing.

Product Description

EDIConnect is an integrated environment that offers a full-range of EDI functionality in a seamless, unified interface. With built-in capabilities for incoming file translation, outgoing transaction construction, acknowledgement generation, process orchestration, and scheduling, EDIConnect delivers the power and scalability to meet the most demanding EDI needs.

Product Description

Ofni Clinical is a clinical data management tool that rapidly creates and implements secure, regulatory compliant clinical trial databases.

Product Description

TrialStat enables you to use one system for all clinical phases including, from build your own EDC for Phase 1; to advanced EDC, CTMS, and Portal functionality for Phase 2 and 3; to flexible electronic patient access for Late Phase.

Product Description

A complete system for creating, deploying, and administering custom data entry applications.

Product Description

Web based SaaS EDC solution for clinical trial management. Features include compliance, data export, and medical coding.

Product Description

Electronic Case Report Form for effective data collection in clinical trials. Audit trail according to FDA/EMA requirements.

Product Description

Simplifies data exchange needs and lowers costs with hassle free connectivity to CBSA (Canada Border Services Agency).

Product Description

EDI Engine is fully equipped with a library of add-ons, or features that enhance industry specific operations, help to reduce manual labor and errors. This is a better solution than wizards that provide a more in-depth process to generate new documents and manage processes such as catalog generation and shipments.

Product Description

EDISPHERE is feature rich, robust, easy to use, and affordable. Unlike most products, EDISPHERE has stronger mapping capabilities, data validation, error reporting, live monitoring and trading partner managing capabilities.

Product Description

Chiapas EDI Enterprise is the shortest and most efficient path to achieving HIPAA compliant transactions.

Product Description

Ediport is the first and only domestic web-edi solution in Turkey specifically designed for the Turkish retail sector.

Product Description

CERF is an award-winning Electronic Lab Notebook (ELN) and collaborative document management solution designed for the creation, capture and ultra-long-term storage of all your records and files.

Product Description

Provantis is the industry-leading GLP-compliant preclinical study management software, supporting every study phase from design to reporting. Trusted globally by study directors and lab managers, it streamlines workflows, ensures data integrity, and accelerates regulatory submissions.