Micramed brings over 28 years of cross-sector experience spanning medical devices, pharmaceuticals and consumer products. Our expertise combines microbiology, quality systems and research and development, supported by hands-on laboratory and project management experience within ISO 17025, ISO 9001, ISO 13485 and MHRA (GMP) compliant environments. Our R&D background includes the development of antimicrobial medical devices and a point-of-care diagnostic for wound care.

We help organisations implement proportionate, scientifically robust microbiological and quality strategies tailored to their products, intended use and regulatory pathway. By translating complex microbiology into clear, practical actions, Micramed delivers solutions that are both compliant and workable in real-world settings.

Micramed bridges the gap between microbiological science and practical regulatory compliance. We provide experienced, independent expertise tailored to organisations that need specialist input without the cost of a full-time resource.

Our approach is collaborative and proportionate—translating standards such as ISO 11137, ISO 11135, ISO 11607, EN 17664, ISO 17025 and the EU MDR Annex I GSPRs into workable solutions that fit your products, processes and business size.

Whether you need strategic guidance, hands-on project support, laboratory oversight or staff training, Micramed delivers clear, pragmatic microbiology you can rely on.