Cavendish Scott, Inc.
Consulting firm providing ISO management-system consulting, internal and supplier auditing, and accredited ISO training. Services focus on implementing and maintaining ISO standards (quality, medical device, environmental, information security, laboratory accreditation, occupational health & safety, aerospace, automotive) and on regulatory alignment for medical devices and laboratory accreditation.
Industries
N/A
Nr. of Employees
small (1-50)
Products
EFI Polymers case study (QMS implementation)
Downloadable case study describing implementation of ISO 9001:2015 and ISO 13485 QMS for a chemical manufacturer.
Gracon Manufacturing case study (ISO 9001 / 13485)
Downloadable case study describing QMS implementation for a manufacturer including sales and purchasing processes and cleanroom setup.
Liteye Systems case study (ISO 9001 / 13485)
Downloadable case study on ISO implementation for an aerospace/defense technology company focusing on QMS alignment with product development.
EFI Polymers case study (QMS implementation)
Downloadable case study describing implementation of ISO 9001:2015 and ISO 13485 QMS for a chemical manufacturer.
Gracon Manufacturing case study (ISO 9001 / 13485)
Downloadable case study describing QMS implementation for a manufacturer including sales and purchasing processes and cleanroom setup.
Liteye Systems case study (ISO 9001 / 13485)
Downloadable case study on ISO implementation for an aerospace/defense technology company focusing on QMS alignment with product development.
Services
Consulting for design and implementation of ISO management systems across standards (9001, 13485, 14001, 17025, 27001, 45001, AS9100, IATF/TS 16949).
Professional internal auditing services, supplier assessments, audit scheduling, evidence collection, and reporting to prepare organizations for certification or accreditation audits.
Accredited lead auditor and internal auditor courses, customized in-company training, and industry-specific training (medical device, aerospace, automotive, labs, cannabis).
Assistance compiling technical documentation, product master files, risk assessments, and management system controls needed for CE marking and alignment with medical device legislation.
Services to prepare laboratories for ISO 17025 accreditation including scope definition, measurement uncertainty, sampling control, and internal audit training.
Consulting for design and implementation of ISO management systems across standards (9001, 13485, 14001, 17025, 27001, 45001, AS9100, IATF/TS 16949).
Professional internal auditing services, supplier assessments, audit scheduling, evidence collection, and reporting to prepare organizations for certification or accreditation audits.
Accredited lead auditor and internal auditor courses, customized in-company training, and industry-specific training (medical device, aerospace, automotive, labs, cannabis).
Assistance compiling technical documentation, product master files, risk assessments, and management system controls needed for CE marking and alignment with medical device legislation.
Services to prepare laboratories for ISO 17025 accreditation including scope definition, measurement uncertainty, sampling control, and internal audit training.
Expertise Areas
- Quality management systems (ISO 9001)
- Medical device QMS and regulatory compliance (ISO 13485, MDR, FDA QSR alignment)
- Laboratory accreditation and measurement quality (ISO 17025)
- Information security management (ISO 27001)
Key Technologies
- ISO management system frameworks
- Process-based internal auditing methodologies
- Accreditation readiness methodologies
- Measurement traceability and uncertainty analysis
News & Updates
Summary of developments in the ISO 9001 revision process and implications for QMS preparation ahead of the 2026 release.
Analysis of proposed integration of FDA QSR with ISO 13485 and guidance for medical device manufacturers.
Announcement and overview of a new ISO amendment integrating climate change considerations into management standards.
Explains upcoming aerospace standard updates and their expected effect on AS9100 implementations.
Summary of developments in the ISO 9001 revision process and implications for QMS preparation ahead of the 2026 release.
Analysis of proposed integration of FDA QSR with ISO 13485 and guidance for medical device manufacturers.
Announcement and overview of a new ISO amendment integrating climate change considerations into management standards.
Explains upcoming aerospace standard updates and their expected effect on AS9100 implementations.