Minimize downtime
Validation downtime impacts production. Kneat automates scheduling, minimizing disruption and maintaining operational efficiency during validation processes.
Track performance consistently
Performance consistency is hard to track. Kneat provides real-time insights into equipment performance, assuring ongoing compliance with validation standards.
Manage equipment upgrades
Obsolescence creates risk. Kneat helps manage equipment upgrades and validations seamlessly, keeping systems up-to-date without compromising compliance.
Standardize across sites
Multi-site equipment validation can be complex, but Kneat standardizes validation processes across locations. Use Kneat to assure uniform compliance across all facilities.
Trusted By
Challenges
Ensuring performance in all scenarios
Equipment validation professionals must ensure consistent performance, mitigate downtime, and adapt to the challenges of validating aging equipment or new technologies across sites.
Other common challenges include:
- Managing revalidation after system upgrades
- Ensuring scalability and reliability of equipment
- Balancing validation with production timelines
THE SOLUTION
Equipment validation, your way
Kneat is trusted by 8 of the world's top 10 life sciences companies. Digitalize and manage any validation process your way, in one easy-to-use, end-to-end solution.
- Create, template, generate, review-approve, test-execute, and trace
- Compliant electronic signatures and audit trail
- Real-time in-document collaboration
- Comprehensive reporting
- Powerful document automation
- Audit readiness, anytime
BENEFITS
Effortless equipment validation
Kneat streamlines equipment validation, reducing downtime and manual errors — improving data integrity, and assuring compliance with regulatory standards.
- Expedite revalidation for faster system upgrades
- Scale validation effortlessly across multiple sites
- Optimize validation without disrupting production
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Customer Success
Case studies
Merck Sharp & Dohme (MSD) reduced validation time by 50%
MSD digitized seven validation processes globally, reducing cycle times by 50%, process steps by 46%, and replacing three QMS systems.
use cases
Analytical Instrument Validation
Audit
Cleaning Validation
Commissioning & Qualification
Computer System Validation
Equipment Validation
Facilities & Utilities Validation
Process Validation
How PCI reduced validation labor hours by 65%
Since 1996, Kneat’s solution partner, Pharmaceutical Calibrations & Instrumentation LLC. (PCI) has provided the Life Science Industry with high-quality equipment and instrument services including Validation,...
use cases
- Commissioning & Qualification
- Equipment Validation
Digitizing validation: a leap in productivity
The client, a US headquartered tier one biotech with multiple facilities in the US and the EU, achieved productivity improvements of 100% after digitizing validation...
use cases
- Commissioning & Qualification
- Equipment Validation
- Facilities & Utilities Validation
Transforming traceability to improve risk mitigation
The customer, a rapidly expanding biotechnology company with over 45,000 employees achieved an 88% time saving on URS, reducing the cycle time from 2 months...
use cases
- Commissioning & Qualification
- Equipment Validation
We were able to demonstrate over 50% cycle time reduction…and process simplification from 15 steps to 8 … because of Kneat we minimized the number of systems we used from 5 to 2.
- Global Executive Director, MSD
Book a demoResults
MORE EFFICIENT FOR c&Q THAN COMPETITOR
Kneat is proven to be 40% more efficient for commissioning & qualification than a leading competitor product. As found in a customer comparative pilot study.
urs approval cycle time reduction
Kneat is proven to reduce user requirements specification approval cycle time by 88%. As found in a customer authored case study.
Reduction in Review-Approval Time
Kneat is proven to reduce review-approval cycle time by 40%. As found in a customer authored case study.
Contract Manufacturing
Accelerate release to production and ensure customer confidence with more efficient, transparent documentation. Perform technology transfer and meet deadlines faster and easier.
Medical Device
Transform the efficiency and compliance of design, process, software, cleaning, equipment, packaging, sterilization, and test method validations.
Biotechnology
Overcome complexity across process, analytical method, equipment, cleaning, computer system, assay, sterilization, and facility validations.
Consumer Health
Get more products to market faster without compromising quality. Improve the efficiency of the entire validation lifecycle for all your consumer health products.
Pharma
Our expert team and industry-leading solution help pharma quality assurance and validation teams overcome compliance and operational challenges every day.
Revolutionize your validation
Digitalize validation your way, with the validation platform trusted by the world’s leading life sciences companies.
Book a demo