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, will present at the eRegulatory Summit to be held in Madrid from April 25 to 27, 2017, on the topic “Regulatory 2020: Technology-Fueled Business Transformation.”
The presentation, scheduled for April 25, 12:00-12:30 p.m., will explore the implications that broader industry drivers – pricing wars, real-time metrics during audits, the digital supply chain, and disruptive technologies – have on regulatory affairs. Pratyusha will identify key success criteria and approaches to develop the 2020 regulatory information management solution landscape that can leverage the emerging business drivers to enable a successful transformation.
“While regulatory affairs might currently wonder why major technology changes taking place across R&D should affect them, the reality is any transformation is only successful if it is managed organization wide and is aligned to the overall business strategy,” Pratyusha says. “All cross-functional departments need to work more collaboratively to successfully navigate through this disruptive technology phase that the life sciences industry faces in the next 5 to 10 years.”
In addition to Pratyusha’s presentation, ArisGlobal will also be exhibiting at the eRegulatory Summit (Stand #20) and is a sponsor of the event. The event will bring together regulatory professionals to explore developments in RIM, Identification of Medicinal Products (IDMP), and the electronic Common Technical Document (eCTD). Attendees are invited to visit Pratyusha and attending ArisGlobal staff to learn about or request a demo of LifeSphere RIMS, the cloud-Based regulatory information management system (RIMS) with full IDMP compliance.
ArisGlobal’s cloud-based solutions facilitate global drug development and regulatory compliance within the life sciences and healthcare industries. Its cloud platform supports the entire product life cycle including clinical development, regulatory affairs, pharmacovigilance and medical communications. Hundreds of drug and device manufacturers, CROs and regulatory agencies leverage ArisGlobal’s advanced technology solutions spanning regulatory information management, risk evaluation and mitigation strategies, medical information and clinical trial management software to make better and more informed decisions, facilitate compliance, reduce risk, and improve operational efficiency. Headquartered in the United States, ArisGlobal has regional offices in Europe, India and Japan. Visit arisglobal.com or follow us via Twitter, LinkedIn or Facebook.