Accessibility Audit and Certification Services

Expert consulting services supporting healthcare facility decision-making regarding medical device selection, procurement, and implementation strategies.

Professional assessment and certification services evaluating electrical safety compliance in hospital critical areas. Identifies risks and recommends solutions to ensure adherence to healthcare electrical safety standards.

Comprehensive testing and certification services for medical devices, including CMA/CNAS accredited laboratory analysis and regulatory compliance documentation. Services support product market registration, quality assurance, and government supervision requirements.

Professional installation and consultation services for mandatory accessibility facilities and medical devices in healthcare facilities, residential, and commercial properties. Includes assessment, installation, and safety compliance support.

Third-party certification and testing services for medical devices and in vitro diagnostics. Provides regulatory compliance assessment, documentation review, and certificate issuance to support market authorization and quality assurance requirements.

Comprehensive testing and certification services for medical devices including safety, performance, and regulatory compliance assessment. Services include chemical analysis, biocompatibility testing, and sterility evaluation to meet international medical device standards.

Factory audit services for medical device manufacturers, providing compliance verification, quality system assessment, and regulatory documentation review. Supports manufacturers in meeting international standards and certification requirements for medical device production facilities.

Professional services for evaluating radiological facility compliance with European regulatory standards and medical device requirements. These audits identify compliance gaps and corrective actions.

Legal and regulatory compliance consulting for medical device registration, approval pathways, and post-market surveillance requirements across different regulatory jurisdictions.

Expert regulatory consulting and pre-certification support for medical devices seeking FCC, CE, UKCA, and other global compliance certifications. Services help reduce time and cost of getting medical products to market.

Comprehensive quality control and assurance services for medical devices, including testing, validation, and compliance verification. Ensures adherence to medical device standards and regulatory requirements.

Certification and regulatory compliance services for medical devices in North American markets. Provides testing, documentation, and approval pathway support for FDA and Canadian regulatory requirements. Leverages global laboratory network with specialized expertise in electrical and electronic medical device evaluation.