Streamlining IT Audits and Compliance for Effective Risk Management
Duration: 1 Hour
An effective IT audits and compliance program is critical for successful risk management in organizations today. Especially in Life Sciences and Medical Devices (LS &MD) companies, IT audits also form the basis for compliance with FDA regulations and mandates such as HIPAA, SOX, 21 CFR Part 11, GXP, CGMP, Part 210-211, Data Retention, Data Privacy, and other privacy and security standards.
An integrated platform for IT Governance, Risk and Compliance (IT-GRC) enables LS & MD organizations to integrate existing processes and tools into a unified approach for IT compliance within the FDA framework.
Join us for this webinar to explore how FDA regulated companies are improving performance and driving down costs of IT compliance by implementing next generation IT-GRC systems. The discussion will cover the benefits of an enterprise-wide platform-based approach for:
- Integrated IT audits and compliance frameworks for FDA companies
- IT risks assessment and control management
- Automated and manual testing of controls specific to LS & MD
- Implementing industry standard frameworks like COBIT, ITIL
- Issue and remediation management for continuous improvement
- Real-time visibility through risk heat-maps, dashboards and reports
Speaker |
Narasimha Kumar
Head, Regulatory IT Compliance, LS&MD Vertical
Tata Consultancy Services |
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Rajesh Venkateswaran
Manager, Strategic Initiatives
MetricStream |
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