
ABOUT KNEAT SOLUTIONS
Kneat Solutions, founded in 2006 and headquartered in Castletroy, Limerick, Ireland, is a global leader in end-to-end validation data management. Specializing in innovative, compliant cloud-based SaaS solutions, Kneat revolutionizes the validation lifecycle by transforming traditional paper-based and hybrid processes into fast, intelligent, transparent digital workflows. Its digital validation platform, Kneat Gx, delivers comprehensive solutions for all validation work processes and activities, empowering highly regulated industries worldwide to achieve operational excellence. Trusted by eight of the top 10 global life sciences organizations and Fortune 500 companies, Kneat Gx accelerates validation timelines, enhances accuracy, and provides actionable insights—setting the gold standard for validation in the life sciences sector.
In 2024, Kneat was recognized as a product leader in the SoftwareReviews study on validation and related software categories, underscoring its commitment to customer satisfaction and value delivery.
FEATURED ARTICLES
-
Discover how evolving regulatory expectations in life sciences present new challenges and opportunities, as well as gain insight into strategies from experts in the field to navigate risk-based validation processes.
-
Watch expert Kathianne Ross explore ALCOA+ principles, audit preparation strategies, and the role of digital validation in enhancing compliance and audit success.
-
The FDA recommends a new approach to computer system validation called Computer Software Assurance. Explore insights that can help you understand CSA and how to implement it in your organization.
-
Optimize your commissioning and qualification (C&Q) process through digital transformation. Delve into the benefits, best practices, and real-world examples of successful digital C&Q implementation.
-
Kneat Gx delivers ROI by reducing costs through paperless validation, increasing efficiency, enabling scalability, and aligning with organizational goals to accelerate life sciences transformation.
-
See how MSD digitized global validation processes achieved over 50% cycle time reduction, streamlined workflows, improved compliance, and enhanced remote collaboration during COVID-19.
-
Explore how the FDA’s CSA guidance simplifies computerized systems validation by emphasizing risk-based approaches, reducing documentation burdens, accelerating testing, and enhancing compliance.
-
Equipment validation ensures pharmaceutical equipment meets regulatory and quality standards. Explore how a structured process ensures compliance, reliability, and high product quality.
-
Discover how to prepare for an audit, from preparation and documentation to streamlined processes and digital validation, ensuring compliance and successful inspections in regulated industries
-
Explore how digital tools enhance validation efficiency, accuracy, and compliance, while reducing costs and cycle times through real-world case studies.
-
Discover how to streamline validation, eliminate paper processes, ensure data integrity, drive ROI, and adopt a digital validation solution.
-
Watch to learn how digital validation streamlines commissioning and qualification (C&Q), improving productivity, compliance, and cost-efficiency across your organization.
-
Explore trends in compliance, audit readiness, digital systems, process efficiencies, emerging KPIs, and the adoption of Pharma 4.0 technologies.
CONTACT INFORMATION
Kneat Solutions
36 E. Main Street, Suite 201
Norristown, PA 19401
UNITED STATES
Phone: +1 (888) 88-KNEAT
Contact: Marilyn Reidy