Industry Perspectives: Concept of Smart ICSRs.
As the Biopharmaceutical Industry moves towards digitalization of the R&D landscape, the classical way of doing Pharmacovigilance will have to change. It is now widely accepted that we cannot wish away ICSRs. Organizations will have to move towards the concept of ‘’Smart ICSRs’’.
How CROs are Uniquely Positioned to Drive Adoption of the TMF Exchange Mechanism
“By leveraging the TMF Reference Model and eTMF Exchange Mechanism Standard, CROs have the power to drive best practices within a variety of therapeutic areas, not only informing the TMF Reference Model itself but also the industry at large.”
How to Ensure a Full-Proof IDMP Strategy in 3 Steps
“As IDMP continues to evolve, here are three critical steps life science organizations can take toward a full-proof strategy that supports changing regulatory requirements.”
In the News
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In the News
GCP update: advice on what to expect and how to prepareLifeSphere’s head of clinical product management, Sonia Araujo, weighs in on the GCP updates in an interview with Outsourcing Pharma. Read the full piece here.
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Data Fabric: Make Safety a Strategic Center by Unlocking the Value of Big DataOur VP of Safety, Beena Wood, shares the power of a well-oiled data fabric. Read the article here.
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How CROs are Uniquely Positioned to Drive Adoption of the TMF Exchange MechanismOur Director of Product Marketing – Clinical, Art Brown, shares insights on the CRO opportunity with TMF exchange. Read more on Applied Clinical Trials here.
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Press Releases
ArisGlobal’s LifeSphere Safety Leaders to Discuss Current Landscape and Future of Data, Automation, and Analytics in Pharmacovigilance at World Drug Safety CongressMarket leading safety platform to lead six sessions across Europe and America. MIAMI, FL – September 20, 2022 – ArisGlobal, the leading provider of life sciences software that automates core drug development…
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LifeSphere RIMS Product Leader to Speak at RAPS Convergence SummitLife sciences veteran Laura Jones to lead a regulatory affairs session regarding investigational products at the signature industry event in Phoenix, AZ. MIAMI, FL – September 9, 2022 – ArisGlobal, the leading provider of life sciences software that automates core drug…
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ArisGlobal Accelerates Growth, Announces Executive EvolutionArisGlobal, the leading provider of life sciences software that automates core drug development functions with its end-to-end technology platform LifeSphere®, today announces an expansion to its C-suite. James Jarrett is the company’s new Chief Financial Officer, Kathleen Turland joins as the first Chief Legal Officer, and Aman Wasan has stepped into the new…
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Blogs
What Does Approachable Automation Mean for Drug Safety Platforms?There’s no doubt that the pharmaceutical industry is well into its ‘age of automation’. A 2021 Industry report found that 83% of life science organizations use some form of automation across their R&D processes—whether that be rule-based automation or technologies enabled by machine learning (ML),…
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How to Select the Right eTMF System and VendorManaging your Trial Master File (TMF) is a necessary, and often tedious task for most clinical stakeholders—but it doesn’t have to be. When teams rely on legacy systems using outdated file sharing technology or homegrown systems leveraging spreadsheets or paper, they open themselves up to vulnerabilities in managing sensitive trial…
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IDMP: How Did We Get Here, and What Does That Mean for Me?Identification of Medical Products (IDMP) has been harmonizing data globally across the drug development lifecycle since 2003. At its core, IDMP uniquely identifies pharmaceutical products and standardizes product information using five international ISO standards to maintain global compliance. For strategic pharmaceutical companies, IDMP can be leveraged beyond that to act…
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ArisGlobal awarded Frost & Sullivan 2021 North America customer value leadership
ArisGlobal recognized by Frost & Sullivan for enabling life sciences companies to accelerate R&D with its LifeSphere platform.
Events
Events
Meet the Experts – TOPRAOctober 18th, 2022 | Vienna, Austria | Join our regulatory experts at TOPRA on Tuesday, October 18th for a free breakfast and networking.
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5 Reasons to Make the Move to Automated Safety Document DistributionAugust 24th, 2022 | 11:00 am ET | For years, both sponsors and CROs have struggled to manage the ever-complex world of Safety Document Distribution. From managing SUSARs to other reporting requirements, managing this process manually can be time-consuming, costly, and creates significant compliance risk. Join our webcast as…
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RAPS Convergence 2022 | RAPSSeptember 11-12, 2022 | Phoenix Arizona, USA | ArisGlobal Booth: 515 | Recognized and respected as the largest annual global, regulatory-focused event,…
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