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Drug Adverse Event Reporting Software is Now Mobile-Friendly

Every one of us at some point will take a medication and likely suffer some sort of adverse reaction. However,…

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New Rules Propose Challenges in Medical Affairs and Pharmacovigilance

What are the Challenges in the Pharma Industry Regarding Data Privacy? Data privacy and data retention seem to become more…

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Regulatory Information Management: Solving the Compliance Challenge with a New Approach

A preview of DIA’s upcoming Regulatory Conference, where ArisGlobal will unveil its revolutionary regulatory information management system software. It’s no secret, the…

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Simplify Requirements for Medical Devices with Regulatory Information Management Systems

Keeping track of all the information required to manage your medical devices on the market is a hugely complex task,…

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A Look Back at Partnerships in Clinical Trials Europe

By Danilo Pavlovic As both a conference attendee and ArisGlobal representative…

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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…

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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…

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CRO (Contract Research Organization) Research & Development Trends

CRO industry grows as increasingly complex R&D trends demand advanced expertise Among today’s CRO, R&D trends, precision-based medicines and immunotherapies for…

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I wrote a post a couple of months ago about the drawbacks of accessing multiple…

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Post by Mathias Poensgen First, it was mandatory to submit results to…

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