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https://catalogartifact.azureedge.net/publicartifacts/cyientlimited1770877590581.cyient_regulatory_compliance-a64ad122-ccd2-478b-a9ce-2fe683de4ca9/c73d7b94-0eff-4667-8825-6e29e9e6ac1c_350x350pxCyientLogo.png

Cyient Regulatory Platform for Healthcare, MedTech and Life Science

โดย Cyient

Solution for transforming QARA workflows for the Medical Device Industry

The solution transforms workflows to address the QARA for Medical Device Industry by using Microsoft AI Copilots or Intelligent Agents that accelerate execution, ensure compliance, improve accuracy, and deliver interactive experiences. Together, Cyient and Microsoft platforms offer industry-first, engineering-led business process solution bring in 3X faster document processing time, 40 % reduced operational cost combined with significant accuracy improvement than the conventional process. Some of the salient feature of the solution.

  • Regulatory Watch Agents: Monitors regulatory changes globally with alerts
  • Checklist Agent: Automatically generates specific regulatory checklists
  • Gap Assessment Agent: Identify gaps and update based on checklist
  • Remediation Plan Agent: Prioritized plan to address compliance gap
  • Audit Assist Agent: Verify against QMS and assist for audit readiness
  • Remediation Execution Agent: Assist documentation for submission
The new and updated mandates from regulatory bodies is a defining moment for medical device companies. For the Chief of Quality, Safety, and Patient Officer, it presents a rare challenge and opportunities to lead with purpose — aligning regulatory rigor with Technology centric innovation and operational excellence

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https://catalogartifact.azureedge.net/publicartifacts/cyientlimited1770877590581.cyient_regulatory_compliance-a64ad122-ccd2-478b-a9ce-2fe683de4ca9/20dfb3b7-0695-4118-b8f1-5ae8ed74d691_CyientRegulatoryPlatform.png