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Oriel STAT A MATRIX provides public training in more than 40 cities across the United States on quality-related topics such as Lean and Six Sigma, medical device quality and regulatory requirements, pharmaceutical quality and regulatory requirements, nuclear regulatory fundamentals, and ISO 9000, AS9100, TL 9000, ISO 14000, and ISO 13485.

In addition, all of our courses can be customized and presented at a location of your choice. Contact us us to learn more.

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Practice Area	Topic	Course Name	Code	Public	On-site
Medical Device RA/QA	FDA Compliance for Medical Devices	510(k) Process for Medical Devices	PMF
Medical Device RA/QA	FDA Compliance for Medical Devices	CAPA Programs for the Medical Device Industry	CAF
Medical Device RA/QA	FDA Compliance for Medical Devices	Course Combo: Understanding FDA's Medical Device QSR and QSIT, Understanding an ISO 13485 QMS	ZFF
Medical Device RA/QA	FDA Compliance for Medical Devices	Design Control Concepts and Implementation	DCF
Medical Device RA/QA	FDA Compliance for Medical Devices	Documenting a GMP/ISO Compliant Quality System	DOF
Medical Device RA/QA	FDA Compliance for Medical Devices	Internal Auditor Training for ISO 13485	IAF
Medical Device RA/QA	FDA Compliance for Medical Devices	Introduction to Process Validation	PVA
Medical Device RA/QA	FDA Compliance for Medical Devices	Lead Auditor Training for ISO 13485	LAF
Medical Device RA/QA	FDA Compliance for Medical Devices	Process Validation Principles and Protocols	PVF
Medical Device RA/QA	FDA Compliance for Medical Devices	Risk Management and Analysis for Medical Devices	FMF
Medical Device RA/QA	FDA Compliance for Medical Devices	Software Verification and Validation Requirements	SVF
Medical Device RA/QA	FDA Compliance for Medical Devices	Sterilization Planning for Medical Devices	STF
Medical Device RA/QA	FDA Compliance for Medical Devices	Understanding FDA’s Medical Device QSR and QSIT	MDF