Division-Specific Requirements
Standardized operational, regulatory, financial, and technological frameworks mandated across all Aevum Zenth business units. Ensure alignment with global compliance standards.
Energy & Power Division
Grid Interconnection Standards
All generation assets must comply with IEEE 1547-2018 and local grid operator technical specifications.
Environmental Impact Assessments
Quarterly EIA submissions required for all renewable and nuclear facilities. Third-party audits mandatory.
Cybersecurity for OT/ICS
Implementation of NIST SP 800-82 and IEC 62443 for all operational technology networks.
Carbon Credit Verification
All offset programs must align with Verra VCS or Gold Standard. Annual reconciliation required.
Zenth Digital Systems
Zero-Trust Architecture
All cloud deployments must enforce NIST SP 800-207 zero-trust principles with continuous verification.
AI Governance Framework
Model cards, bias audits, and human-in-the-loop validation required for all production ML systems.
Data Residency & Sovereignty
Customer data must be stored within jurisdictional boundaries per local regulatory mandates.
Supply Chain Software Validation
SBOM generation and vendor risk assessments mandatory for all third-party dependencies.
Aevum Aerospace & Defense
Configuration Management
Full traceability from requirements to design, test, and production per AS9100 Clause 8.3.6.
Export Control Compliance
All dual-use technologies require DDTC/BJA licensing and end-user verification protocols.
Flight Safety & Airworthiness
FAA/EASA certification pathways and DO-178C/DO-254 compliance for embedded software/hardware.
Secure Communications
Classified data handling per NIST SP 800-171 and CMMC Level 3 readiness requirements.
Zenth Health Sciences
Clinical Trial Governance
ICH-GCP E6(R2) compliance, IRB/IEC approvals, and DSMB oversight mandatory for all phases.
Manufacturing Quality Systems
21 CFR Part 211 (cGMP) and EU Annex 1 compliance for sterile drug production facilities.
Pharmacovigilance & Reporting
Real-world safety monitoring and SUSAR reporting within 15/7-day regulatory windows.
Medical Device Validation
ISO 13485 and FDA 21 CFR Part 820 adherence for all diagnostic and therapeutic devices.
Cross-Divisional Mandates
Information SecurityAll divisions must maintain ISO 27001 certification and conduct bi-annual penetration testing.
Financial ReportingConsolidated monthly P&L, cash flow, and balance sheet submissions via Aevum ERP within 10 business days.
ESG & SustainabilityQuarterly carbon footprint tracking, waste reduction metrics, and diversity/inclusion reporting.
Vendor Risk ManagementThird-party due diligence, contract compliance audits, and supply chain resilience assessments.
Workforce StandardsGlobal HR policies, anti-bribery training, whistleblower protections, and executive compensation alignment.
R&D IP ProtectionPatent filing protocols, invention disclosure forms, and cross-divisional technology transfer governance.
Templates & Documentation
Compliance & Governance Contacts
Internal Audit
Quarterly audits, risk assessments, and operational compliance reviews across all divisions.
audit@aevumzenth.comLegal & Regulatory
Contract compliance, litigation support, and jurisdictional regulatory advisory services.
legal@aevumzenth.comESG & Sustainability Office
Carbon tracking, impact reporting, and sustainability certification coordination.
esg@aevumzenth.comIT Security Operations
Threat monitoring, incident response, and cybersecurity framework implementation.
security@aevumzenth.com