Best Practices in Safety Signal Analytics — Managing Today and Preparing for Tomorrow
With up to 30-50% annual growth in adverse event cases, how ...
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Breakthrough 2027 brings together life sciences leaders, industry regulators and experts, to explore the future of AI in life sciences.
With up to 30-50% annual growth in adverse event cases, how ...
Artificial intelligence (AI), machine learning, deep learning, natural language processing ...
Silos have long plagued the life sciences industry, and nowhere ...
The Shift to the Cloud Historically, firms relied heavily on ...
Data is the lifeblood of businesses today. Data informs strategy ...
On June 9th, 2020 ArisGlobal held a webinar titled “Pharmacovigilance and ...
In the age of Covid-19, the cause of a global ...
In the last of our three-part blog series, we share the poll results to the question "What concerns do you have when it comes to automating PV process?" and analyze the responses. Read the blog to see how your responses might compare.
In order to stay compliant with NMPA requirements (submitting all post-marketing ADRs in ICH E2B (R3) format), drug manufacturers are required to procure an electronic safety database that is.....
Pharmacovigilance is at a crossroads. The best, most innovative way forward for PV departments may well be automation, as they address the challenges (or market pull factors) and opportunities (or technology push capabilities).
ArisGlobal is a pivotal partner in the life sciences industry, specializing in solutions that drive drug development, safety monitoring, and regulatory compliance. We collaborate with more than 220 global life sciences companies, CROs, and government health authorities, including leading biopharmaceutical firms and regulatory bodies such as FDA, Health Canada, and NMPA.
Headquartered in the United States, ArisGlobal has regional offices in Europe, India, Japan and China.
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