Jurisdiction

International

20 compliance framework entries tagged under this jurisdiction. Open each card for official documentation links.

  • 20 frameworks

AS9100

Official

AS9100D Quality Management Systems: Requirements for Aviation, Space, and Defense Organizations

AS9100D is the aviation, space and defense quality management system standard, published by SAE International and built on ISO 9001:2015.

SAE Quality Management Aerospace

CAP Accreditation

Official

CAP Laboratory Accreditation Program

College of American Pathologists accreditation programs for laboratories, including the Laboratory Accreditation Program and CAP 15189.

CAP Lab Accreditation Healthcare

Sustainability Reporting

Official

ESG and Sustainability Reporting Standards

Index of sustainability disclosure standards and rules, including GRI, ISSB (IFRS S1 and S2), SASB, the EU CSRD and SEC climate rules.

GRI IFRS Foundation Environmental All

GCP

Official

Good Clinical Practice (ICH E6(R3))

International standard for the design, conduct and reporting of clinical trials (ICH E6(R3)), issued by FDA as final guidance in the US.

FDA ICH Clinical Research Biotech & Life Sciences

ICH E6(R3) GCP

Official

ICH E6(R3) Good Clinical Practice

ICH's international guideline for the ethical and scientific conduct of clinical trials, revised as E6(R3), with Annex 2 adopted in June 2026.

ICH Clinical Research Biotech & Life Sciences

IEC 62304

Official

IEC 62304 Medical Device Software: Software Life Cycle Processes

IEC international standard for medical device software life cycle processes; the current text is the 2006 edition plus Amendment 1 (2015).

IEC International Standards Medtech

IEC 62366-1

Official

IEC 62366-1 Medical Devices: Application of Usability Engineering

IEC standard for applying usability engineering to medical devices to reduce use-related risk. Current: IEC 62366-1:2015+AMD1:2020.

IEC ISO International Standards Medtech

ISO 13485

Official

ISO 13485:2016 Medical Devices Quality Management Systems

International standard from ISO setting quality management system requirements for organizations involved in the medical device life cycle.

ISO Medical Device Biotech & Life Sciences

ISO 14001

Official

ISO 14001 Environmental Management Systems

ISO 14001:2026 is the ISO standard specifying requirements for an environmental management system, with guidance for use.

ISO Environmental All

ISO 14971

Official

ISO 14971:2019 Medical Devices: Application of Risk Management to Medical Devices

ISO international standard for risk management across the life cycle of medical devices, including in vitro diagnostic devices; third edition 2019.

ISO International Standards Medtech

ISO 28000

Official

ISO 28000 Security and Resilience: Security Management Systems

ISO 28000:2022 is the ISO standard specifying requirements for a security management system, including aspects relevant to the supply chain.

ISO Supply Chain All

ISO 9001

Official

ISO 9001 Quality Management Systems: Requirements

ISO international standard setting requirements for a quality management system. Current edition: ISO 9001:2026.

ISO Quality Management All

ISO/IEC 27001

Official

ISO/IEC 27001 Information Security Management Systems

ISO/IEC 27001:2022 is the ISO and IEC standard specifying requirements for an information security management system (ISMS).

ISO IEC Cybersecurity Biotech & Life Sciences

ISO/IEC 27017

Official

ISO/IEC 27017 Information Security Controls Based on ISO/IEC 27002 for Cloud Services

ISO/IEC guidance on information security controls for cloud service providers and customers, based on ISO/IEC 27002. Current edition: 2026.

ISO IEC Cybersecurity Technology

ISO/IEC 27018

Official

ISO/IEC 27018:2025 Protection of PII in Public Clouds

ISO/IEC guidelines for protecting personally identifiable information in public clouds where the provider acts as a PII processor. 2025 edition.

ISO IEC Cybersecurity Technology

MDSAP

Official

Medical Device Single Audit Program (MDSAP)

MDSAP lets one recognized auditing organization audit a device maker for the FDA, Health Canada, TGA, ANVISA and Japan's MHLW and PMDA.

FDA Health Canada Medical Device Biotech & Life Sciences

NIST CSF 2.0

Official

NIST Cybersecurity Framework (CSF) 2.0

NIST guidance for managing cybersecurity risk, organized into six functions: Govern, Identify, Protect, Detect, Respond and Recover.

NIST Cybersecurity Healthcare

PCI DSS

Official

Payment Card Industry Data Security Standard (PCI DSS)

PCI Security Standards Council standard for protecting payment account data wherever it is stored, processed or transmitted. Current: v4.0.1.

PCI SSC Cybersecurity Healthcare

PCI DSS

Official

PCI Data Security Standard (PCI DSS) for Healthcare Payments

PCI Security Standards Council standard for protecting payment card data, current version v4.0.1, applying to any entity handling card data.

PCI SSC Financial Healthcare

RDM and FAIR

Official

Research Data Management and FAIR Principles

Research data management and sharing practices, including the FAIR principles and the NIH Data Management and Sharing Policy for NIH-funded work.

NIH Clinical Research Biotech & Life Sciences