The Vogel Group supports defense and military technology projects with processes based on international standards and supplemented by the requirements of AQAP 2110 and AQAP 2113. This allows us to meet the expectations of military clients regarding process reliability, documentation, verification, and traceability. Our quality management system is based on ISO 9001, but in safety-critical projects, it is extended by AQAP-specific requirements, for example, regarding responsibilities, the involvement of government quality assurance bodies, and formal acceptance processes.
Quality Management System (QMS)
Our QMS provides the framework for all activities in development, production, and service. It defines clear responsibilities, establishes the structure of processes, and integrates defense-related contractual requirements into project planning at an early stage. This includes internal audits, management reviews, and the systematic handling of nonconformities. Upon request, we ensure complete transparency regarding our quality-relevant processes for regulatory bodies—such as GQA organizations. This includes regulated access to documentation, test reports, and production-related procedures.
Clearly defined responsibilities and contact persons
Standardized processes for defense projects
Transparent access for GQA/regulatory bodies
Risk and opportunity management
Sound decisions in the defense sector require early and structured risk management. From the very beginning of a project, we analyze potential risks related to technical requirements, supply chains, changes, and configuration statuses. This analysis is continuously updated, and necessary measures are documented and monitored. In addition to minimizing risks, we also consider opportunities, such as process optimizations or alternative technical solutions that can improve the project's progress.
Ongoing risk monitoring throughout the project
Focus on supply chain and change risks
Opportunities are actively evaluated and leveraged
Configuration management
Clear and traceable product configuration is essential in the defense industry. We ensure that all changes, versions, and technical statuses are meticulously documented. This includes configuration management plans, defined release processes, and complete transparency throughout the product lifecycle. Systematic status records and traceable change logs enable clients and testing organizations to precisely assess the current configuration status at any time.
Documented change and version statuses
Verifiable configuration history
Lifecycle support with clear processes
Management of external suppliers
Since the supply chain is a crucial component of quality assurance, we also transfer the relevant requirements to our sub-suppliers. This includes the transfer of contractual obligations, the evaluation and monitoring of partners, and measures to ensure conformity and traceability. Particular attention is paid to preventing counterfeit materials, which is why we employ appropriate testing and verification procedures. Furthermore, we grant government quality assurance bodies the necessary access to supplier processes, provided this is contractually stipulated.
Mandatory flow-down of safety-relevant requirements
Regular supplier evaluations
Mechanisms established to prevent counterfeiting
Production processes and service provision
Our production follows clearly defined testing, measurement, and release procedures. Testing equipment is regularly calibrated and documented, critical characteristics are recorded separately, and all products are clearly marked. Through standardized processes in manufacturing, storage, and shipping, we ensure that product quality remains unchanged until delivery. The preparation of certificates of conformity or participation in acceptance tests by government agencies is also part of our service scope, if contractually required.
Defined testing and release processes
Traceable identification of critical characteristics
Support for official approvals
Documentation and verification
Reliable documentation is a key component of defense technology quality assurance. Therefore, we maintain detailed test reports, configuration records, validation documents, and supplier records that are fully traceable at all times. Documents are managed in an auditable manner, older versions are archived, and current versions are made available in a controlled manner. Clients have access to all relevant documents, enabling acceptance tests, audits, or GQA inspections to be carried out without delay.
Audit-proof document management
Access for clients at any time
Comprehensive test and validation reports
Internal Audits, Reviews, and Improvement
To maintain robust quality management, we regularly conduct internal audits specifically focused on safety- and contract-related processes. Trained auditors assess the effectiveness of these processes, document the results, and initiate optimization measures. Management reviews support these activities through the systematic evaluation of key performance indicators, resources, and measures. This ensures that our system not only meets formal requirements but also continuously improves.
Audit Program for Defense-Relevant Processes
Qualified Auditors
Continuous Improvement Firmly Embedded
Contract Requirements and Tailoring
Defense-related contracts often differ significantly in their quality requirements. Therefore, we conduct targeted tailoring at the beginning of each project: We analyze the relevant sections of the standard, derive specific requirements for the project, and integrate these into our planning and production processes. This also includes the creation or implementation of quality plans in accordance with relevant guidelines, if contractually stipulated.
Project-specific adaptation of requirements
Integration of relevant standard sections
Quality plans according to client specifications
Traceability, product safety, and acceptance testing
All materials, components, and assemblies are managed in such a way that they remain traceable throughout the entire process. Product safety is ensured through the analysis of critical characteristics, functional dependencies, and potential failure effects. Acceptance processes by clients or regulatory quality assurance bodies are based on verifiable test and documentation records and can be supported both on-site and digitally.
Complete traceability
Analysis of critical characteristics
Acceptability through complete documentation
Special requirements in the defense sector
In addition to traditional quality assurance, we also consider security and regulatory requirements, such as those relating to export controls, confidentiality, or NATO-specific regulations. Furthermore, we support clients in accessing defense-related markets, for example, through documented evidence of our quality management and established processes for dealing with regulatory bodies. Our clear focus on AQAP requirements enables seamless collaboration on sensitive projects.
Consideration of export and confidentiality regulations
Support for defense market requirements
Clear interfaces with authorities and GQA
