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Aris Global White Papers, Product Overviews and Technology Briefs

Please select one or more papers from the list below by checking the box to the left of each paper and clicking "Continue" at the bottom of the page. Aris Global reserves the right to screen requests.

Pharmacovigilance & Safety

Best Practices for Migrating to a New Safety System
When a company decides to install a new system, consolidate multiple application instances, or upgrade to a new version of their safety system, it is imperative to ensure minimum downtime and data loss. Aris Global consultants have executed numerous safety system migrations to ARISg. In the process, they have developed strategies and best practices that are used for rapid migration with minimum risk.
agEncoder Position Paper: The advantages and strengths of Aris Global's centralized coding and dictionary
Medical coding departments require powerful tools to streamline the process of transforming verbatim terms into standard coded terms that are fully compliant with regulatory review and approval standards. Just as important as having the necessary functionality and capabilities, Aris Global believes that customers should consider a vendor's experience, their proven integration capabilities, support for global requirements, long-range vision and industry knowledge in selecting a software partner for a coding solution. Request this position paper to learn by Aris Global stands out as the smart choice.
Addressing Key Challenges in Drug Safety (Strategy Focus)
In this March 2008 report from Datamonitor, this leading analyst firm examines pharmacovigilance technology solutions designed to alleviate the challenges in drug safety management. Aris Global is clearly noted as a leading provider in this space.
ARISg 6.3: Comprehensive Solution for Clinical Safety and Pharmacovigilance
This Product Overview provides a more detailed capabilities overview of ARISg's most recent version, including its updated user interface, extended support for blinding/unblinding, personalized user dashboard, integrated metrics reports, enhanced communication management, and much, much more.
agXchange IRT and OST: Inbound Receipt and Triage / Outbound Submission Tracking of Adverse Event Information
This Product Overview provides a more detailed capabilities overview of agXchange IRT and OST, the newest modules in the agXchange electronic exchange platform.
Achieving Total Safety
This white paper provides an overview of contemporary safety, pharmacovigilance and risk management. We review the business drivers for moving from mere compliance to total commitment to safety and introduce you to Total Safety, the integrated suite of solutions from Aris Global.
Automating Safety-to-Investigator Reporting
This white paper examines the common challenges with safety-to-investigator reporting and discusses the new alternatives for managing clinical safety report distribution to your key stakeholders. You are introduced to agXchange SIR, the first commercial solution that provides powerful business and technical benefits, such as reducing costs, increasing productivity and ensuring compliance with regulatory authorities.
Affiliate Safety Tracking
Aris Global has made great strides in delivering on the vision for achieving end-to-end paperless safety. This paper discusses the challenges that headquarters have in capturing all inbound safety issues, tracking compliance at each affiliate and partner, ensuring data quality of received reports, and performing effective follow-up tracking with appropriate documentary evidence. You are introduced to agXchange IRT and OST, that enable companies to deploy cost-effective, end-to-end safety item tracking from receipt to submission.

Regulatory Affairs

Managing Global Product Portfolios with End-to-End Regulatory Tracking
This Aris Global white paper examines the business challenges life sciences are facing regarding regulatory affairs and introduces Register™, the market-leading solution for managing global product portfolios with end-to-end regulatory tracking.
Regulatory and Manufacturing: A Strategy for Bridging the Compliance Gap
In this paper, we examine the challenges and solutions of bridging the compliance gap between manufacturing and regulatory in the life sciences. Readers are given a brief introduction to how Register™ helps drive excellence in manufacturing through better integration, information exchange, record keeping, and effective change-management facilities.
Register: Overview of the Planning Module
Register 5 includes an integrated and enhanced product planning component that automates the tracking of registrations against global and local project plans. This paper provides an overview of the new planning module, addressing the challenge that many life science organizations face for managing the numerous activities and resources associated with global regulatory submissions.

Clinical Research & Operations

Integrated e-Clinical Systems: Evolution or Creation?
Written by Dr. Sylva Heghinian Collins, this white paper examines the two approaches to achieving integrated systems: creating an entire suite of software from scratch, or evolving the patchwork of existing systems toward a unified whole. You will learn how integrating these components into a seamless whole can lead to wholesale improvements in the speed, cost and quality of clinical information processing.
New Approach to Clinical Trials Management: Execution versus Tracking
Successful trials are the lifeblood of a life sciences company, making the effective planning, coordination, collaboration and communication of trials a business-critical activity. Aris Global and SAP have taken on the challenge of co-innovating a new approach to address the clinical trials process. This paper details the agClinical NW™ solution that delivers CTMS functionality that provides comprehensive, end-to-end process support.
Safety-to-Investigator Reporting
This Product Overview provides a detailed capabilities overview of the agXchange SIR module, which enables organizations to automate the distribution of clinical safety reports and other clinical documentation to investigators, IRBs, ethics committees and other stakeholders.

Medical Information

Medical Information Management: Using Advanced Technology to Protect Patients and Brand Equity
In recent years, the roles and responsibilities of medical information departments have evolved from simply fielding questions to becoming major contributors, to meeting the company's business objectives, and to building brand equity. This paper examines the business drivers for providing users access to medical information and introduces you to agInquirer™; a comprehensive web-based medical information management system that facilitates the full request-and-response lifecycle.

Hosted Software-as-a-Service Offerings

agOnDemand: Removing the Barriers to Total Safety
The paper provides details on agOnDemand's unique differentiators and carefully explains how this solution offers ready-to-use solutions that are cost effective and require very little set up before they are up and running.

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