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RIMS + ERP - The Tag Team of Future of Compliance

Global regulatory compliance mandates continue to increase in number and evolve rapidly in complexity. Most of these regulations aim directly or indirectly to ensure the quality and traceability of medical products delivered to the market. Ensuring the safety of the patient through monitoring that compliant products are delivered to the...
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ARISg and ARISj: Extending a Worldwide Pharmacovigilance Program into the Japanese Market - White paper

An integrated safety and pharmacovigilance system with worldwide business processes helps companies realize significant productivity benefits. This position paper summarizes Aris Global’s Total Safety global solution for companies that are either headquartered in Japan or have Japanese affiliates and focuses on the key benefits of deploying a single safety and...
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Affiliate Safety Tracking - White Paper

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...
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Automating Safety-to-Investigator Reporting - White Paper

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...
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Achieving Total Safety - White Paper

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.   * denotes required field * First Name...
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agXchange IRT and OST: Inbound Receipt and Triage / Outbound Submission Tracking of Adverse Event Information - White Paper

This product overview provides a more detailed capabilities overview of agXchange IRT and OST, the newest modules in the agXchange electronic exchange platform.   * denotes required field * First Name * Last Name * Your Email Organization Name Phone Which best describes your current need?: — Select One —I...
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ARISg 6.3: Comprehensive Solution for Clinical Safety and Pharmacovigilance - White Paper

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.   * denotes required field * First Name * Last Name * Your Email...
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agEncoder Position Paper: The advantages and strengths of Aris Global's centralized coding and dictionary - White Paper

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. Request this position paper to learn how agEncoder stands out as the smart choice.   * denotes required field * First Name...
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Best Practices for Migrating to a New Safety System - White Paper

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...
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agComposer Product Overview - White Paper

Aris Global’s agComposer software is designed specifically to enable global life science organizations to schedule, create, manage and track periodic and aggregate reports as required by the various regulatory agencies. This white paper focuses on the key challenges faced in preparation of periodic and aggregate reports and explains the benefits...
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Simplifying the DSUR Creation Process Using agComposer™: A conversation with Wim Cypers, Vice President, Regulatory Affairs - White Paper

With the DSUR coming into force in September 2011 in the European Union, many life sciences companies are rushing to put together a process to comply with the regulation. In this paper Wim Cypers, VP Regulatory SPU at Aris Global, discusses the challenges normally faced by companies in preparing the...
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The $1B Question: How to Never Miss Processing Adverse Events across Your Business (and Always Pass Regulatory Inspections)? - Webcast Replay

We’ve all seen the headlines related to regulatory non-compliance penalties and know the risks, but meeting the challenge of capturing and properly reporting ALL adverse events is a daunting one. Initial receipt of product safety issues is generally from diverse, globally-distributed sources and may be channeled through local safety offices,...
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