The IRT Landscape: Regulations, Challenges and Solutions – White Paper
The US Medical Device Market is the world’s largest at an estimated US $127.1bn in 2013 and is very highly regulated. Clear and detailed information relating to devices must be submitted to the FDA for...
View ArticleArisGlobal Announces First-To-Market Agile Clinical Research Organization...
Pay-As-You-Grow Service Offering Delivers Competitive Edge to CROs looking for more Sponsors and Clinical TrialsCHICAGO, IL. DECEMBER 14, 2016 — ArisGlobal, a leading provider of integrated,...
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Medical affairs teams at the heart of Phase IV studies
Recent article demonstrates the pivotal role of medical affairsMedical Affairs teams have long played a role in the life cycle of a drug going to market and staying in market. But, is their role...
View ArticleRegulatory Submissions Webinar
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View ArticleArisGlobal Wins Growing Client Base for Drug Safety and Risk Management...
CHICAGO, IL. January 3, 2017 — ArisGlobal, a leading provider of cloud-based software solutions for the life sciences, has announced four new clients that are using its integrated safety intelligence,...
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Need Help Solving Your Complex Safety Challenges?
Get help at upcoming Pharmacovigilance and Risk Management Strategies ConferenceJust as 2017 looks to be another strong year for pharma, it will continue to pose challenges for safety and...
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If You’re a CRO, You’ll Want to Read This Success Story
As the outsourcing trend continues to grow, many biopharmaceutical and pharmaceutical companies find themselves needing to partner with CROs (contract research organizations) that are seasoned and can...
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A level playing field: Realizing the importance of emerging CROs
With declining R&D budgets, increased competition from larger CROs and patent expirations, emerging CROs have evolved from being non-core service providers to being integral partners in the...
View ArticleArisGlobal Releases agClinical 3.3
Chicago, Illinois, January, 23 2017 — ArisGlobal, a leading provider of integrated, cloud-based software solutions for life sciences, announces agClinical 3.3, the latest version of its comprehensive...
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New Rules Challenging Data Privacy Rentention Processes
Data privacy and data retention seem to become more complicated by the day in the realm of medical affairs and pharmacovigilance. I am beginning to think that there really is no solution. With the GDPR...
View ArticleArisGlobal Announces a Milestone of More Than 70 Top-Tier Life Sciences...
Chicago, Illinois. January 25, 2017 Customers Turn to Cloud Platform for Security, Flexibility and Efficiency ArisGlobal, a leading provider of integrated, cloud-based software solutions for life...
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Regulatory Information Management: Solving the Compliance Challenge with a...
A preview of DIA’s upcoming Regulatory Conference, where ArisGlobal will unveil its revolutionary regulatory information management system software. It’s no secret, the main role of any pharmaceutical...
View ArticleArisGlobal Introduces LifeSphere™ Regulatory Information Management System...
Next-Generation, Cloud-Based Regulatory Information Management System Features Integrated Industry Standard Practices and Advanced IDMP Compliance Chicago, Illinois, February 6, 2017 — ArisGlobal, a...
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Adverse Event Reporting Software Gets a New Friend: Mobile
Every one of us at some point will take a medication and likely suffer some sort of adverse reaction. However, while some of us will actually read the product label and identify the possible adverse...
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Promises, promises: Finding a CTMS that gives you what you need – Now!
Time and again you hear the same refrain: “It will be in the next release”. But in the meantime, you’re struggling to cope because you need certain features and functionalities for your clinical trials...
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Tomorrow’s Medical Information Tools Today
We know from our customers that for many medical information teams, being tasked with meeting pharmacovigilance obligations ensuring global compliance, as well as providing up-to-date, consistent and...
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A Secret Weapon to Act on Your IDMP Assessment
IDMP If you’re in Regulatory Affairs, you know the IDMP-compliance-truck is headed your way. Which questions though are plaguing your team? Wondering how to work on the recommendations from an initial...
View ArticleArisGlobal Regulatory Expert to Present at eRegulatory Summit on Industry...
CHICAGO, IL. APRIL 7, 2017— ArisGlobal, LLC, a global leader in providing cloud-based software solutions for the life sciences, has announced that Pratyusha Pallavi, Product Manager for Regulatory,...
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Think Big: Regulatory Affairs Must Prepare to Respond to Strategic Business...
Regulatory Affairs Regulatory affairs departments are accustomed – and even open — to change and adapting their technology and processes in response to compliance and business pressures. Typically,...
View ArticleClinical Research IO to Collaborate with ArisGlobal to Improve Data Quality...
CAMBRIDGE, MA. March 16, 2017— Clinical Research IO (CRIO), a Cambridge-based technology company that has developed the first eSource system built and marketed directly to clinical research sites,...
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