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Consulting & Auditing

In business since 1968, Oriel STAT A MATRIX fuses our expertise in life sciences, quality management systems, and performance improvement methodologies to help our customers meet regulatory requirements and boost results.


Learn more about our consulting capabilities in the following practice areas.

>Medical Device
Medical Device
RA/QA Consulting

Leverage our team's experience to achieve and maintain US FDA and global regulatory compliance with training and consulting support for the entire product life cycle. 

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Quality System
Quality System Audits for FDA's QSR, ISO 13485, MDSAP

Find expert, outside support for supplier, internal, and FDA mock audits. Unlike registrars and notified bodies, our auditor consultants are allowed to both identify deficiencies and help you design effective solutions. 

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Connected Medical Devices
Connected Medical Devices, SaMD & IOMT 

Full full life cycle quality and regulatory support for manufacturers of digital medical technology - includes training, auditing, and consulting. 

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ISO 9000 & Related Standards

Implement a QMS that complies with globally recognized management standards like ISO 9001 and ISO 13485.

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Oriel STAT A MATRIX’s Goal

Help our life science customers meet regulatory requirements, boost efficiency, and improve patient outcomes

Get answers right now. Call
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US OfficeWashington DC


EU OfficeCork, Ireland

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+353 21 212 8530

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