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RA/QA Training for the Life Sciences Industry

Oriel STAT A MATRIX provides public training across the United States on 22+ Medical Device RA/QA topics including EU MDRISO 13485 and Risk Management. We also offer online, virtual instructor-led training, and all of our courses can be customized and presented as private trainings for your organization.  Contact us to learn more.

Filtered by: Pharmaceutical RA/QA
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Pharmaceutical RA/QA

New! Design Control for Combination Products

Topic Regulatory Compliance for Pharmaceuticals

Code DCP

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DCP
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New! Applying Usability Principles to Drug Delivery Systems with IEC 62366-1:2020

Topic Regulatory Compliance for Pharmaceuticals

Code UDP

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UDP
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New! Combination Product Device Supplier Management Training

Topic Regulatory Compliance for Pharmaceuticals

Code SQP

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SQP
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New! Managing Risks in Combination Products and Drug Delivery Systems

Topic Regulatory Compliance for Pharmaceuticals

Code RMP

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RMP
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New! Combination Products: From Regulatory Strategy to Postmarket Surveillance

Topic Regulatory Compliance for Pharmaceuticals

Code CPP

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CPP
Public
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New! Inspection and Audit Readiness Training for Pharmaceutical Manufacturers

Topic Regulatory Compliance for Pharmaceuticals

Code IRP

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IRP
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New! Process Validation in the Pharmaceutical Industry

Topic Regulatory Compliance for Pharmaceuticals

Code PVP

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PVP
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New! Root Cause Analysis for Combination Products and Drug Delivery Systems

Topic Regulatory Compliance for Pharmaceuticals

Code RCP

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RCP
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New! Data Integrity and Electronic Records Training for Pharmaceutical Companies (ALCOA+ and FDA 21 CFR Part 11)

Topic Regulatory Compliance for Pharmaceuticals

Code DIP

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DIP
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Oriel STAT A MATRIX’s Goal

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

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