GxP validationthat accelerates, not constrains
Empower your teams with AI-driven validation technology and decades of domain expertise in one unified platform.
Equipment validation for tomorrow's standards
Stop tracking calibrations in spreadsheets, storing protocols in shared drives, and running commissioning on paper.
Bridge the gap between AI innovation and GxP compliance
Life sciences leaders need AI's transformative power without compromising patient safety or regulatory confidence. The old validation rules no longer apply.
Meet tomorrow's standards using future-ready technology
Embrace AI-driven workflows for trend identification, predictive maintenance, and improved compliance.
Learn how CDMOs are managing multiple client priorities while maintaining validated states. Discover strategies for scalable, flexible validation that grows with your business.
30-40% faster validation across multiple sites
See how a growing biotech unified validation control and freed their teams to focus on breakthrough discoveries.
Need deeper insights into your validation processes?
Learn more about Res_Q's dashboards and reporting capabilities.
30-40% faster validation across multiple sites
See how a growing biotech unified validation control and freed their teams to focus on breakthrough discoveries.
Need deeper insights into your validation processes?
Learn more about Res_Q's dashboards and reporting capabilities.
30-40% faster validation across multiple sites
See how a growing biotech unified validation control and freed their teams to focus on breakthrough discoveries.
The Future of Life Sciences Validation is Here: Are You Ready?
At a live roundtable event held in February 2024, three leaders from industry, IT, and Quality came together in Boston to discuss the future of GxP validation, including the role AI will play and the how to prepare for its inevitable integration. Read our whitepaper based on the illuminating discussion, hosted by Bryan Ennis (Founder, Sware) and featuring speakers Nathan McBride (Senior Vice President, IT at Xilio Therapeutics) and Aryaz Zomorodi (Associate Director, Systems Quality, SpringWorks Therapeutics).
is Here: Are You Ready?
At a live roundtable event held in February 2024, three leaders from industry, IT, and Quality came together in Boston to discuss the future of GxP validation, including the role AI will play and the how to prepare for its inevitable integration. Read our whitepaper based on the illuminating discussion, hosted by Bryan Ennis (Founder, Sware) and featuring speakers Nathan McBride (Senior Vice President, IT at Xilio Therapeutics) and Aryaz Zomorodi (Associate Director, Systems Quality, SpringWorks Therapeutics).
Quality Must Play a Pivotal Role at Every Stage
Today’s consensus is that AI is both acceptable and valuable but must exist firmly within existing IT-quality control frameworks. Quality leaders must be prepared to work closely with their IT counterparts to implement GxP solutions that offer explainable, transparent AI technologies, as well as develop robust SOPs that establish parameters for effective and responsible use.
Proper data governance forms a crucial foundation for success: put simply, bad data in leads to bad data out. Using our established lens, it’s important to ask: is our data curation process up to modern standards; do we have the right people overseeing data ops; and finally, do we have the right tools in place to store and organize our data, either via warehousing or data lakes?
Webinars
As part of our commitment to supporting organizations implementing AI for GxP, Sware is proud to present the following webinars:
As AI capabilities push into GxP regulated business functions, how can Quality and IT teams partner to ensure they are properly controlled? Join us as a panel of experts walks you through emerging practices for how Life Sciences companies can integrate AI-based solutions into GxP functions responsibly.
Panelists:
Bryan Ennis, President, Sware
Jamie Hijimans, President and Strategic CTO, Global Exponential Technologies (GxT)
Michelle Vuolo, Head of Quality, Tulip Interfaces, Inc.
Madhavi Ganesan, Director, Lifesciences Advisory, KPMG
In this presentation, featured speaker Bryan Ennis, President, Sware, explores important topics that Quality and IT leaders should consider when developing an organizational path towards the use of AI within the GxP ecosystem, including:
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GxP use cases where AI is emerging
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Quality System practices for managing AI in GxP
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The role of vendors, IT and Quality in controlling GxP AI
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Investments needed to scale AI capabilities into future GxP use cases
Upcoming Events and Webinars
As part of its commitment to supporting organizations implementing AI for GxP, Sware is proud to participate in the following events and webinars:
JULY 10, 2024 / 11 AM EST
As AI capabilities push into GxP regulated business functions, how can Quality and IT teams partner to ensure they are properly controlled? Join us as a panel of experts walks you through emerging practices for how Life Sciences companies can integrate AI-based solutions into GxP functions responsibly.
Topics included:
- GxP use cases where AI is emerging
- Quality System practices for managing AI in GxP
- The role of vendors, IT and Quality in controlling GxP AI
- Investments needed to scale AI capabilities into future GxP use cases
SEPT 12, 2024 / 11:15 AM EST
As AI capabilities push into GxP regulated business functions, Quality and IT teams can partner together to ensure they are properly controlled. In this discussion, we 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, including:
-
GxP use cases where AI is emerging
-
Quality System practices for managing AI in GxP
-
The role of vendors, IT and Quality in controlling GxP AI
-
Investments needed to scale AI capabilities into future GxP use cases
"Sware provided invaluable support by bringing deep industry knowledge, experience, and connections to our project. Now, when I’m sitting across the table from a large life sciences client, I can speak their language and discuss compliance knowing that as audit processes evolve, we’ll be in a strong position to evolve with them."
Use cases
Track every asset from FAT through decommissioning in one system.
Roll out validated equipment protocols across facilities instantly.
Monitor change and receive alerts when revalidation is needed.
Agentic AI converts SME walkthrough videos to executable scripts automatically.
Understand equipment validation status at a glance. Know what needs attention today.
Automate alerts before calibrations expire and integrate directly with your CMMS.
A clinical-stage biotech reduced validation time from days to hours while managing 30+ quarterly releases. See how they moved from paper-based tracking to automated workflows.
Validation workstreams that weren’t in Res_Q took days. Those same workstreams, once moved into the Res_Q system, take hours.”
Senior Director, Development Informatics
Molecular Medicine Company
"We highly recommend Res_Q for its simplicity and effectiveness. [The] software is exceptionally user-friendly, enabling streamlined audits through controlled auditor access. All validation activities are consolidated within a single app, ensuring consistency and transparency. The prebuilt templates simplify implementation and promote uniform validation processes."
Jim H | Director of Quality
"Sware's Res_Q software is exceptionally user-friendly, enabling streamlined audits through controlled auditor access. All validation activities are consolidated within a single app, ensuring consistency and transparency. The prebuilt templates simplify implementation and promote uniform validation processes. We highly recommend Sware for its simplicity and effectiveness."
Jim H
Andelyn Biosciences
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