Resource Center
Archived Webcasts
Pharmacovigilance & Safety
agXchange IRT and OST: New Strategies for Automating the Receipt and Submission of Adverse eEvents
View this webcast presentation to learn about the latest trends and effective practices for inbound receipt and triage and outbound submission tracking.
ARISg 6.2: Improving the Case Processing Life Cycle
View this webcast presentation to learn about the new and leading functionality that facilitates case processing, shortens the time for data entry, reduces the manual exchange of paper and improves compliance.
Successful Strategies and Best Practices for Receiving and Submitting Adverse Events
View this webcast presentation to learn the latest trends and successful methods for receiving, reporting, and submitting safety cases. Discover how Aris Global's hosted solutions, agXchange IRT and OST, can help you automate and streamline these critical processes.
agSignals™ and agComposer™: Maximizing Safety and Minimizing Risk
View this webcast presentation to learn about agSignals, a streamlined and efficient solution that provides end-to-end process support for signal detection and risk/benefit management activities. agSignal's optimized database, powerful front-end reporting and analysis tools, trending reports and business analytics will be demonstrated. You will also learn how agComposer enables end-to-end periodic and aggregate reporting and can be integrated with clinical trial, regulatory and medical information databases. When integrated with each other, agSignals and agComposer facilitate the creation of aggregate reports in accordance with regulatory requests and commitments.
Regulatory Affairs
Single Source of Authoritative Data: Eliminating Manual and Redundant Regulatory Tracking
View this webcast presentation and look at how companies can make better and more informed business decisions while lowering the costs for tracking regulatory submissions and monitoring obligations with regulatory authorities.
Beyond SPL R4 Compliance: Achieving Operational Efficiencies in Regulatory & Labeling
View this webcast to learn how industry leaders Aris Global and i4i (Infrastructure for Information) help companies achieve compliance while realizing operational efficiencies for an end-to-end label management and registration tracking solution.
Register™ 5.1: Leading the Way in Tracking Post-Marketing Commitments
View this presentation to learn how Register overcomes the challenges of tracking and managing commitments and obligations that can lead to critical compliance and registrations issues if not initiated or completed on a timely basis.
Register™ 5: Automating the Tracking of Regulatory Submissions
For most life science organizations it is the coordination of activities and resources that has the highest impact on the quality, speed and cost of a submission and ultimately its success. Many companies currently rely on manual processes to create, manage, distribute and track project plans associated with regulatory submissions and have no global view of potential delays or resource conflicts. Register 5 addresses this gap by automating the definition, distribution and reporting of project plans at the global and local/regional level.
Regulatory and Manufacturing: A Strategy for Bridging the Compliance Gap
Company reputation, brand identity and financial performance are powerful indications of an organization's success...or failure. With product recalls and market withdrawals on the increase, pharmaceutical, biotechnology and medical device companies significantly improve their chance for success when regulatory and manufacturing bridge the compliance gap. By working from a centralized hub of approved specifications, companies can make better and informed business decisions while lowering the costs for tracking regulatory submission and monitoring obligations with regulatory authorities.
View this webcast presentation to learn about a proven strategy that better ensures global product portfolio management.
Medical Information
Medical Information Management: Protecting Your Patients and Brand Equity
With an increased focus on regulatory information compliance, today's medical communications organization has a direct impact on a company's brand equity, customer satisfaction, risk management and ongoing regulatory compliance. As the all-important face of the organization, this is the team who is in direct contact with the public who use, the investigators who monitor, the healthcare professionals who prescribe, and the sales and marketing professionals who promote their products. Regardless of the topic-proper dosage levels, potential effects of drug combinations, reactions and adverse events, off-label use and self-medication-all inquiries need quick, consistent and accurate responses and distribution of information.
View this archived presentation to learn how your organization can manage the full medical information request-and-response lifecycle to improve customer service levels and streamline business processes.
Clinical Research and Operations
Total Clinical: The Many Benefits of Integrating with Safety and Clinical Systems
Total Clinical™ delivers a level of integration that is smart, meaningful and value added - finally delivering seamless interoperability across clinical systems. Attend this webcast to hear about a best-in-class suite of clinical safety, EDC, coding and CTMS applications that truly deliver on the "enter data once & share across the enterprise" promise.
agCapture: Integration with Oracle Clinical
Oracle Clinical is the CDMS platform of choice for many companies. Attend this webcast to understand how agCapture can be used to automatically export EDC data into Oracle Clinical, to give your organization a single repository where all your clinical trials data can be stored.
agCapture: Improving Trial Outcome with Integrated Decision Support
Imagine what can be achieved if, according to your study protocol, your EDC could automatically adjust dosing schedules based on the clinical data of each individual trial subject. Attend this webcast to learn how agCapture is integrated with award-winning decision support technology that provides integrated protocol guidance help to investigators to ensure the "right treatment for the right patient" and provides investigators with real-time advice and best practice guidelines.
Clinical Operations: Best Practices for Automating Safety-to-Investigator Reporting
Learn the latest trends and successful methods for distributing clinical safety reports and other clinical documentation to investigators, IRBs, ethics committees and other stakeholders. receiving, reporting, and submitting safety cases. Discover how Aris Global's hosted solution, agXchange SIR™, can automate and streamline safety report distribution while delivering significant cost saving, efficiencies, and better compliance.
agXchange SIR: Safety Report Distribution - Overhauling a Time-Critical Responsibility
Learn about the challenges of managing safety-to-investigator report distribution and how agXchange SIR, the hosted software-as-a-service solution from Aris Global, can overhaul a manual, costly and time-intensive nightmare into an automated report distribution process that delivers a quick return on your investment and improves compliance.
Hosted, Managed Software
Hosted Drug Safety: Removing the Barriers of Cost, Complexity and Constraints
Explore the cost savings and compliance benefits that a growing number of companies are experiencing with agOnDemand™, the hosted drug safety system from Aris Global®. You will learn about the Molecular Insight Pharmaceuticals case study and the Switch-to-Save program underway that can deliver a fully validated, highly secure system in less than 5 weeks.
Hosted Drug Safety & Outsourced Case Processing: Your One-Stop, Cost-Effective Solution for Achieving Safety Control
Attend this webcast to learn how companies are able to achieve significant cost savings as they now can focus on their core safety and business activities while meeting regulatory obligations.
Hosted Regulatory Tracking: Managing Regulatory Obligations with Greater Speed and Efficiency
Attend this webcast to learn about agOnDemand RT™, hosted software for cost-effectively automating the tracking and managing of all regulatory affairs activities on a global basis.
