Medical device testing and certification service ensuring compliance with global regulatory standards including MDR, IVDR, and MDSAP. BSI provides notified body assessments, ISO 13485 audits, and conformity evaluation to support safe market placement of medical devices and in vitro diagnostics.
Manufactured by
BSI Group Ltd.
Milton Keynes, United Kingdom
We guide you on your journey to meet global standards, promote safety, and enhance trust with your clients. As the world's first national standards body, our unrivalled global expertise and long-standing commitment to public benefit and innovation sets the benchmark for regulatory excellence. Our comprehensive portfolio offers you a wide range of proven regulatory and quality management services to support you in bringing compliant devices to market efficiently and safely. CE certification UKCA Certification ISO 13485 certification MDSAP Certification – Medical Device Single Audit Program and many more specialized solutions tailored to your regulatory needs.
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