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Recent Events
Big data, the specter of AI, and the long-awaited switch to CSA have IT and Quality leaders asking: “what’s next?” 3 industry experts discuss what your life sciences company should be doing now to prepare for the industry's future.
Read the WhitepaperAre you in a good state for the next tech advancement? Quality experts will discuss risk assessment and risk management approaches that enable companies to be more efficient, and therefore keep up with technology and bring on new systems (which will have more maintenance).
WATCH ON-DEMANDAre you in a good state for the next tech advancement? Quality experts will discuss risk assessment and risk management approaches that enable companies to be more efficient, and therefore keep up with technology and bring on new systems (which will have more maintenance).
WATCH ON-DEMANDNews
We are excited to announce that Sware is partnering with Verista to help life sciences companies realize Pharma 4.0 by providing advanced and innovative digital validation solutions.
Read MoreWe are excited to announce that Sware is partnering with Benchling to accelerate digital R&D transformation for biotechs globally — by enabling adoption of modern software, purpose-built for science.
Read MoreRecent & Upcoming Events
In today’s rapidly evolving life sciences landscape, treating validation as a series of isolated projects is no longer optimal. In this webinar hosted by Xtalks, our expert panel discusses the critical importance of treating validation as a core element of an organization’s quality management system (QMS).
Watch On-DemandMaking the jump from CSV to CSA will require close collaboration between IT and Quality teams – and a solid understanding of the role future technologies will play. Join our expert panel for an engaging webinar, hosted by Xtalks, to learn more about the key role collaboration, technology, and market forces will play in tomorrow's compliance landscape.
WATCH ON-DEMANDIn this presentation at the 5th Annual GxPCloud Compliance Summit in Boston, featured speaker Bryan Ennis, President, Sware, will explore important topics that Quality and IT leaders should consider when developing an organizational path towards the use of AI within the GxP ecosystem.
WATCH ON-DEMANDJoin us for a roundtable discussion on the future of software validation in life sciences. Over the course of our discussion, industry thought leaders will help you navigate the challenges imposed by constant software releases, new regulatory mandates, and complex validation needs.
Read the WhitepaperLife sciences companies will share the challenges they were facing, their experiences implementing a SaaS based Computer Systems Validation (CSV) platform, and the business value achieved. There will be a variety of perspectives including R&D, clinical research, regulatory affairs, and IT.
WATCH ON-DEMANDExplore the future state of technology across pharmaceutical manufacturing and the challenges companies will face. What is going to be required and how can life sciences companies best position themselves to adopt transformational technologies and drive business value?
Watch On-DemandPre-conference workshop with Sware CEO, Bryan Ennis: A Practical Guide to Maintaining Digital Validation in the Life Sciences Industry.
Session with Sware CEO, Bryan Ennis: Business Leadership: Validation — The Digital Transformation Time Forgot.
How are paper-based systems still standard practice for validation in a world that includes cloud computing and individualized therapies?
AI as a technology foundation presents unique issues that will affect validation.
With little guidance currently within the life sciences industry and regulators, presenters reflect on the upsides and the concerns around AI and then delve into a pragmatic discussion centered upon validating and managing changes in an AI-based system.
Join Bryan Ennis, the co-founder and CEO of Sware, as he leads an engaging discussion among a group of your validation peers.
The discussion will revolve around the current compliance landscape of GxP systems and explore digital validation trends. The panel will discuss the challenges and advantages that we all face as the industry progresses - and how quality and IT can best work together for a brighter future
Watch On-DemandJoin your colleagues for a collaborative conversation around the future trends of digital validation and ways to transform your organization’s quality mindset.
Join your colleagues for a collaborative conversation around the future trends of digital validation and ways to transform your organization’s quality mindset.
Featured Resources
The future of life sciences validation and compliance is not so far away. Already, we are seeing life sciences companies rush to integrate AI where possible, while at the same time striving to manage risk with fewer human and material resources available.
Read the WhitepaperLearn how Nuvolo is leveraging a combination of Sware's Res_Q Platform and expert resources to deliver a fully GxP compliant offering to the life sciences industry, enabling Nuvolo and their customers to meet business goals.
Read the case studyManual computer software validation processes cost life sciences organizations up to 30% in additional project budget. As companies struggle to keep up with a surge of app and software integrations, they incur validation debt: the mounting cost of stretched resources, blanket testing, and missed GxP requirements.
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