How to Ensure a Full-Proof IDMP Strategy in 3 Steps
Robin Schilling, Product Manager for LifeSphere IDMP, discusses the core requirements for making sure you are ready for the pending IDMP regulations. Check out the full article on Pharmaceutical...
View ArticleHow Clinical Operations Can Accelerate Through De-risking Clinical Trials
Advances in clinical trial design and technology are significant contributors to medical progress. However, they also hamper clinical operations and data management professionals’ understanding of...
View ArticlePMI Life Sciences Goes Live with LifeSphere Safety to Modernize Global Safety...
Two LifeSphere Safety products–MultiVigilance and Reporting and Analytics–are powering PMI’s pharmacovigilance efficiencies in multiple languages with automation and machine learning. MIAMI, FL — June...
View ArticleIDMP: 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...
View ArticleHow CROs are Uniquely Positioned to Drive Adoption of the TMF Exchange Mechanism
Our Director of Product Marketing – Clinical, Art Brown, shares insights on the CRO opportunity with TMF exchange. Read more on Applied Clinical Trials here. The post How CROs are Uniquely Positioned...
View ArticleArisGlobal Announces New Brand Identity for Award-Winning Life Sciences SaaS...
Global market-leading technology solution unveils new, strategic branding to align with significant corporate growth and surge in product adoption MIAMI, FL — July 19, 2022 — ArisGlobal, the leading...
View ArticleData Fabric: Make Safety a Strategic Center by Unlocking the Value of Big Data
Our VP of Safety, Beena Wood, shares the power of a well-oiled data fabric. Read the article here. The post Data Fabric: Make Safety a Strategic Center by Unlocking the Value of Big Data appeared...
View ArticleHow to Select the Right eTMF System and Vendor
Managing 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 When teams rely on legacy systems using outdated file sharing...
View ArticleDIA China 2022
December 8-11, 2022 | Suzhou China | ArisGlobal Booth C3 A16 | DIA China 2022 Meeting will be held in October in an in-person conference format in Suzhou, will continue to bring the key focuses on...
View ArticleTOPRA Annual Symposium 2022
October 17-19, 2022 | Hotel Vienna Park, Vienna, Austria | Join ArisGlobal at Exhibition Booth #7 at TOPRA Annual Symposium 2022. The Symposium is open to anyone interested in regulatory affairs and...
View ArticleGCP update: advice on what to expect and how to prepare
LifeSphere’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. The post GCP update: advice on what to...
View ArticleWorld Drug Safety Congress Americas
October 4-5, 2022 | Boston, MA, USA | ArisGlobal Booth: 28 | The World Drug Safety Congress Americas will bring together 1000+ top leaders and stakeholders in biopharma to discuss the key challenges...
View ArticleWorld Drug Safety Congress Europe
September 27-29, 2022 | Amsterdam, the Netherlands | ArisGlobal Booth: 33/34 | Explore the use of big data and AI in pharmacovigilance, examine benefit-risk management strategies and patient-centric...
View ArticleClinical Proventa International Roundtable
September 20th, 2022 | 11am – 1pm ET | How to move from manual to automated safety distribution systems; A session meant for sponsors and CROs dealing with complexity or compliance issues and looking...
View ArticleRAPS Convergence 2022 | RAPS
September 11-12, 2022 | Phoenix Arizona, USA | ArisGlobal Booth: 515 | Recognized and respected as the largest annual global, regulatory-focused event,… The post RAPS Convergence 2022 | RAPS appeared...
View Article5 Reasons to Make the Move to Automated Safety Document Distribution
August 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...
View ArticleArisGlobal’s LifeSphere Regulatory IDMP Product Leader Invited to Chair...
Nonprofit Institute works in close collaboration with industry and government to identify and develop standards- and conformance-based solutions to national and global priorities. MIAMI, FL — Aug. 22,...
View ArticleChina’s PegBio Selects LifeSphere by ArisGlobal for Safety Case Processing
LifeSphere Safety increases its customer footprint, further solidifying its safety market leadership position. MIAMI, FL — Oct. 27, 2022 — ArisGlobal, the leading provider of life sciences software...
View ArticleClinical Operations Meeting East Coast
November 9, 2022 Cambridge, MA, USA ArisGlobal to Host a Roundtable discussion Tired of the same conference experience? Real discussions and genuine networking are often promised, but not always...
View ArticleWebinar: The Future of Safety Signal Analytics is Now With LifeSphere Clarity
December 7, 2022 | 11:00 am ET Webinar Register Now The Future of Safety Signal Analytics is Now With LifeSphere Clarity Get an exclusive look at the newest innovation from LifeSphere, by ArisGlobal –...
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