Pursuit of Excellence

Owen Mumford is widely recognised for our expertise in maintaining high-quality standards in the development and manufacturing of medical devices. With a strong emphasis on quality, we have built a reputation as a trusted provider of reliable and safe healthcare solutions.

At the core of Owen Mumford's quality expertise is a commitment to meeting and exceeding regulatory requirements and industry standards. We adhere to strict quality management systems and processes throughout our operations to ensure consistent quality control at every stage of product development, from design and manufacturing to distribution and post-market surveillance.
 

Navigating the complexities of compliance

Owen Mumford's regulatory expertise is a critical aspect of our commitment to delivering high-quality medical devices that meet global regulatory standards. Through our deep knowledge, proactive approach, and collaborative efforts, we ensure compliance, by successfully navigating the ever-evolving regulatory landscape, ultimately benefiting patients and healthcare providers worldwide.

Accreditation and Standards

We adhere to all relevant international standardisation guidelines, including:

Case study: Streamlining Quality Processes With ETQ
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ISO 13485:2016 Standard Certification – OM United Kingdom
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Medical Device Single Audit Program MDSAP
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ISO 13485:2016 Standard Certification – OM Malaysia
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Environmental Management System
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Medical Device Directive
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Quality Policy OMQA0027
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B Corp Certification
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Further reading

R&D

Research and Development

Research and Development
Manufacturing Capabilities

Manufacturing Capabilities

Manufacturing Capabilities

Patient Focused Design

Patient Focused Design