Expert ISO & Regulatory Consulting
Wintersmith Advisory helps organizations implement and maintain ISO systems for compliance and performance.
Elevating Systems. Enhancing Performance.
Wintersmith Advisory delivers practical, precision-driven support to strengthen your management systems, meet regulatory requirements, and improve how your organization runs.
Frameworks and Standards
ISO 9001 – Quality Management Systems
AS9100 – Aerospace Quality Management
ISO 14001 – Environmental Management
ISO 45001 – Occupational Health & Safety
ISO/IEC 27001 – Information Security Management
ISO/IEC 27701 – Privacy Information Management
ISO 31000 – Risk Management Guidelines
ISO 14064-1 – Greenhouse Gas Emissions Accounting
GRI Standards – Sustainability Reporting
ISO 26000 – Social Responsibility Guidance
SA8000 – Social Accountability
ISO 37001 – Anti-Bribery Management
ISO 13485 – Quality management for medical devices
ISO 14971 – Risk management for medical device manufacturers
ISO/IEC 17025 – Competence of testing and calibration laboratories
ISO/IEC 20000-1 – IT service management systems
ISO 21001 – Educational organization management systems
ISO 22000 – Food safety management systems
ISO 22301 – Business continuity management systems
ISO 26000 – Social responsibility guidance
ISO 30401 – Knowledge management systems
ISO 31000 – Risk management guidelines
ISO 35001 – Biorisk management for laboratories and related organizations
ISO 37001 – Anti-bribery management systems
ISO/IEC 42001 – Artificial intelligence management systems
ISO 50001 – Energy management systems
ISO 56001 – Innovation management systems
ACMP Standard for Change Management – Organizational change management framework
EU MDR (2017/745) – European Medical Device Regulation
GRI Standards 1–3 – Sustainability reporting principles and general disclosures
IWA 48:2024 – ESG-related competencies for boards and governing bodies
21 CFR Part 111 – Dietary supplement manufacturing practices (U.S. FDA)
21 CFR Parts 210/211 – Pharmaceutical manufacturing practices (U.S. FDA)
21 CFR Part 820 – Quality system regulation for medical devices (U.S. FDA)
GDPR – General Data Protection Regulation (EU data privacy)
CMMI – Capability Maturity Model Integration (process improvement)
CMMC – Cybersecurity Maturity Model Certification (U.S. DoD contractors)

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