The Future of Regulatory Affairs
Pratyusha Pallavi, Associate Director BU – Regulatory at ArisGlobal to Present “Automating Health Authority Correspondence and Commitments on a Unified Regulatory Platform” MIAMI, FL Febuary 5, 2020 –...
View ArticleArisGlobal Attending the SCOPE Summit in Orlando
MIAMI, FL Febuary 12, 2020 – ArisGlobal, the leading provider of life sciences software that automates core drug development functions for over 250 global life sciences companies, is thrilled to be a...
View ArticleArisGlobal to Co-Present “Enhancing Operations: Enabling Digital...
MIAMI, FL Febuary 12, 2020 – ArisGlobal, the leading provider of life sciences software that automates core drug development functions for over 250 global life sciences companies, is thrilled to be a...
View ArticleArisGlobal Insights – Interview with Sondra Pepe
This is the first in a four-part blog series that examines the Clinical, Medical Affairs, Regulatory, and Safety business units at ArisGlobal.In November 2019, Sondra Pepe joined ArisGlobal as Senior...
View ArticleArisGlobal Insights – Interview with Emmanuel Belabe
This is the first in a four-part blog series that examines the Clinical, Medical Affairs, Regulatory, and Safety business units at ArisGlobal.In November 2019, Sondra Pepe joined ArisGlobal as Senior...
View ArticleArisGlobal Insights – Interview with Pratyusha Pallavi
ArisGlobal Insights: Interview With Pratyusha Pallavi Senior Director of Regulatory Product Management This is the third in a four-part blog series that examines the Clinical, Medical Affairs,...
View ArticleArisGlobal Insights – Interview with Sandeep Mahagaonkar
ArisGlobal Insights: Interview With Sandeep Mahagaonkar Associate Director of Medical Affairs and Quality This is the fourth in a four-part blog series that examines the Clinical, Medical Affairs,...
View ArticleArisGlobal Hosts Optimizing Adverse Event Reconciliation in Medical Affairs...
Blog ArisGlobal Hosts Optimizing Adverse Event Reconciliation in Medical Affairs Webinar On March 11, 2010, ArisGlobal hosted a webinar titled Optimizing Adverse Event Reconciliation in Medical...
View ArticleMultinational Medical Device and Healthcare Organization Embraces LifeSphere®...
SUMMARY A large multinational medical device and health care organization was looking for a way to bring automation and a higher degree of control to their existing Medical Literature Monitoring (MLM)...
View ArticleLinical Adopts ArisGlobal as Primary Global Safety Management System
MIAMI, FL January 22, 2020 – Linical, a market-leading, midsized, global contract research organization (CRO), announced they have adopted ArisGlobal as their primary global safety management system....
View ArticleMajor Tobacco Manufacturer Selects LifeSphere® MultiVigilance to Automate All...
A multinational tobacco products manufacturing company recently selected ArisGlobal’s LifeSphere® MultiVigilance 10 for their global safety vigilance needs. MIAMI, FL Febuary 11, 2020 – ArisGlobal,...
View ArticleThe Future of Regulatory Affairs
Pratyusha Pallavi, Associate Director BU – Regulatory at ArisGlobal to Present “Automating Health Authority Correspondence and Commitments on a Unified Regulatory Platform” MIAMI, FL Febuary 5, 2020 –...
View ArticleArisGlobal Attending the SCOPE Summit in Orlando
MIAMI, FL Febuary 12, 2020 – ArisGlobal, the leading provider of life sciences software that automates core drug development functions for over 250 global life sciences companies, is thrilled to be a...
View ArticleArisGlobal to Co-Present “Enhancing Operations: Enabling Digital...
ArisGlobal to Co-Present “Enhancing Operations: Enabling Digital Transformation with Next-Gen Technology” at World Drug Safety Congress Americas This event has been postponed until September 01-02,...
View ArticleArisGlobal Insights – Interview with Sondra Pepe
This is the first in a four-part blog series that examines the Clinical, Medical Affairs, Regulatory, and Safety business units at ArisGlobal. In November 2019, Sondra Pepe joined ArisGlobal as Senior...
View ArticleArisGlobal Insights – Interview with Emmanuel Belabe
This is the first in a four-part blog series that examines the Clinical, Medical Affairs, Regulatory, and Safety business units at ArisGlobal. In November 2019, Sondra Pepe joined ArisGlobal as Senior...
View ArticleArisGlobal Insights – Interview with Pratyusha Pallavi
ArisGlobal Insights: Interview With Pratyusha Pallavi Senior Director of Regulatory Product Management This is the third in a four-part blog series that examines the Clinical, Medical Affairs,...
View ArticleArisGlobal Insights – Interview with Sandeep Mahagaonkar
ArisGlobal Insights: Interview With Sandeep Mahagaonkar Associate Director of Medical Affairs and Quality This is the fourth in a four-part blog series that examines the Clinical, Medical Affairs,...
View ArticleArisGlobal Hosts Optimizing Adverse Event Reconciliation in Medical Affairs...
Blog: ArisGlobal Hosts Optimizing Adverse Event Reconciliation in Medical Affairs Webinar On March 11, 2010, ArisGlobal hosted a webinar titled Optimizing Adverse Event Reconciliation in Medical...
View ArticlePresenting the All New Automation/Pharmacovigilance Knowledge Hub
Learning Made Easier: Presenting the All New Automation/PV Knowledge Hub Pharmacovigilance (PV) is the process in drug development that ensures safe, innovative, and high-quality medicinal products...
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