Kneat Gx

MSB Docs simplifies digital document management for businesses of all sizes with secure, compliant, and legally binding Electronic Records and Electronic Signatures (ERES). It complies with US FDA 21 CFR Part 11, EU GMP Annex 11, and EU eIDAS (SES, AES, QES), making it ideal for regulated industries like healthcare and life sciences, while enabling cross-industry use across the EU. In India, MSB Docs adheres to the IT Act 2000 and supports DSC, Aadhaar-based eSignatures, and eStamping, making it the most trusted digital documentation platform. Trusted by leading organizations in pharma, BFSI, government, and education, MSB Docs offers: 1. eSign – Compliant digital signatures 2. CRA App – Simplified Clinical Research Associate workflows 3. Smart Forms – Dynamic, logic-based digital forms 4. eStamp – Legally valid, tamper-proof stamping MSB Docs enables organizations to digitize, manage, and automate document workflows.

Res_Q is an AI-powered GxP validation and compliance management platform developed by Sware for organizations operating in regulated life sciences environments. The software centralizes computerized system validation, documentation, risk assessments, testing, and approval workflows within a cloud-based platform. Its agentic AI capabilities automate routine validation activities, monitor progress, and identify milestones requiring human attention. Res_Q provides intelligent risk scoring, automated document processing, video-to-test-script generation, and dashboards for analyzing validation activities. The platform supports Good Clinical Practice (GCP), Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and AI system validation requirements. Integration capabilities connect Res_Q with enterprise applications, testing tools, and quality management systems while maintaining traceable records and audit trails.