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Cyient Regulatory Platform for Healthcare, MedTech and Life Science
โดย Cyient
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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
สรุปย่อ
https://catalogartifact.azureedge.net/publicartifacts/cyientlimited1770877590581.cyient_regulatory_compliance-a64ad122-ccd2-478b-a9ce-2fe683de4ca9/20dfb3b7-0695-4118-b8f1-5ae8ed74d691_CyientRegulatoryPlatform.png