White paperThe Enterprise Framework for Compliant, Scalable AI
Download now

How to Leverage USDM's Vendor Audit of Oracle Supply Chain Management Cloud

Learn how USDM's independent vendor audit of Oracle Supply Chain Management Cloud and the Vendor Assurance Report let life sciences teams leverage Oracle's validation evidence to cut testing burden the FDA's least-burdensome, risk-based way.

How to Leverage USDM's Vendor Audit of Oracle Supply Chain Management Cloud

Summary

The FDA has long encouraged life sciences companies to leverage high-quality vendor documentation rather than re-create validation evidence for its own sake. Each year, as part of USDM Cloud Assurance™, USDM audits Oracle as an independent qualified third party and publishes the Oracle Vendor Assurance Report. This article explains how you can use that report — alongside Oracle's own testing — to minimize your IQ, OQ, and PQ burden for Oracle Supply Chain Management (SCM) Cloud while keeping your validation aligned to your intended use.

From the General Principles of Software Validation (2002) to Computer Software Assurance for Production and Quality System Software — Guidance for Industry (September 2025)

The FDA has continuously promoted leveraging vendor documentation to support a risk-based least burdensome approach to software quality. The FDA states if vendor documentation is in place and of good quality, it can and should be leveraged as documented evidence in establishing that the software core functionality has been validated.1

While life science companies are ultimately responsible for ensuring that software meets their own intended use, their focus should not be on re-creating documentation for documentation's sake. Instead, they should focus on ensuring the software works for their end-to-end intended use. This mindset is at the heart of Computer Software Assurance (CSA) and modern validation lifecycle management: think critically, test where risk lives, and reuse credible evidence wherever it already exists. Below, we share how you can utilize USDM and Oracle activities to minimize your validation and testing burdens. This benefit applies to all partners in USDM's Cloud Assurance ecosystem.

The core idea: You remain accountable for fitness-for-intended-use, but you do not have to independently re-prove what Oracle already builds, tests, and maintains. The Vendor Assurance Report turns Oracle's evidence into something you can cite.

Oracle Vendor Assurance Report

Annually, as a part of the USDM Cloud Assurance™ service, and to replace the need for individual audits, Oracle hosts USDM as an independent qualified third party to audit their design, development, testing, qualification, and maintenance methodologies. The audit is specifically scoped to the Oracle Fusion infrastructure and Oracle Supply Chain Management (SCM) Cloud, Clinical One and Argus Safety for compliance to FDA software compliance standards.

Results of the audit are compiled into the Oracle Vendor Assurance Report, a comprehensive report and reference document, which not only provides a summary of the audit, but also cites all source material reviewed as a part of the audit activities, and provides direct links to all publicly available content. Think of it as your own Dewey Decimal System for Oracle software development lifecycle (SDLC) and testing documentation. Bottom line: USDM audits Oracle, so you don't have to.

Because the audit is performed by an independent qualified third party, it also strengthens your third-party risk management posture — giving quality and procurement teams a defensible, repeatable basis for trusting a critical cloud vendor.

USDM audits Oracle, so you don't have to — and the Vendor Assurance Report becomes your reference library of credible, citable validation evidence.

Leveraging Vendor Documentation

Map your validation activities to the audit

Use the Vendor Assurance Report to determine which traditional validation activities Oracle has already substantiated, then concentrate your own effort on configuration and intended-use testing. The framework below follows the familiar IQ / OQ / PQ structure.

Infrastructure, Back-Up, Disaster Recovery, and Installation Testing
Installation Qualification (IQ)

By qualifying the cloud infrastructure, verifying the applications, and following their own procedures for items such as backup and recovery, access control, and the instance installation, Oracle has done much of this work for you. You can leverage the summary of documentation reviewed during the audit, and detailed in the Vendor Assurance Report, as your evidence.

  • Leverage Oracle's core functionality testing. Reference the appropriate sections of the Vendor Assurance Report in your Traceability Matrix and include a copy of it as evidence in your Validation package.
  • Focus on qualifying the configuration; verify your instance has been configured for your intended use.

Functionality and Workflow Testing
Operational / Performance Qualification (O/PQ)

While testing of functionality will still be required from an intended use standpoint, certain aspects of the traditional O/PQ activities can be leveraged from the audits. The most prominent is a detailed review of Oracle's functional testing activities – the overall SDLC, including unit, regression, integration, and boundary testing of the out-of-the-box (core) functionality. You can leverage the summary of test documentation reviewed during the audit and detailed in the Vendor Assurance Report, as your evidence.

  • Leverage Oracle's core functionality testing. Reference the appropriate sections of the Vendor Assurance Report in your Traceability Matrix and include a copy of it as evidence in your Validation package.
  • Focus OQ testing on high-risk core and custom functionality that impacts product quality and patient safety.
  • Focus PQ testing on your use of the system. End-to-end workflow to establish confidence that your process operates as intended and is reproducible.

Throughout, keep your access controls, audit trails, and electronic records aligned to 21 CFR Part 11, and confirm that the configured system preserves data integrity across your supply chain workflows.

USDM Cloud Assurance™

Whenever software is changed, an analysis should be conducted not just for validation of the individual change, but also to determine the extent and impact of that change on the entire system. As part of the Cloud Assurance™ core-level subscription for Oracle SCM Cloud service, USDM provides an impact assessment of upcoming releases that includes guidance on the required regression testing based on the high-risk areas of the system's core functionality.

Additionally, you can upgrade to USDM's premium-level Cloud Assurance™ subscription, if you would also like for USDM to provide a customer-specific analysis of Oracle's SCM Cloud releases to ensure all aspects of your unique system configuration are tested according to your inherent risk – within your specific testing environment. Regression test scripts are executed for each release specific to each customer's configuration. Read more about what it means to be Cloud Assurance Certified.

FAQ: Leveraging USDM's Oracle SCM Cloud Vendor Audit

What is the Oracle Vendor Assurance Report?

It is the comprehensive report USDM produces after auditing Oracle as an independent qualified third party. It summarizes the audit of Oracle's design, development, testing, qualification, and maintenance methodologies, cites all source material reviewed, and links to publicly available content — serving as a reference library for Oracle's SDLC and testing documentation.

Which Oracle products does the audit cover?

The audit is scoped to the Oracle Fusion infrastructure and Oracle Supply Chain Management (SCM) Cloud, Clinical One, and Argus Safety, assessed for compliance to FDA software compliance standards.

Does leveraging the report remove my validation responsibility?

No. Your company remains responsible for ensuring the software meets your own intended use. The report lets you cite Oracle's already-substantiated core functionality and infrastructure testing as evidence, so you can focus your effort on configuration qualification and high-risk, intended-use OQ and PQ testing.

How does USDM Cloud Assurance handle Oracle SCM Cloud releases?

The core-level subscription provides an impact assessment of upcoming releases with guidance on required regression testing for high-risk core functionality. The premium-level subscription adds a customer-specific analysis and executes regression test scripts against your unique configuration within your own testing environment for each release.

How does the audit support third-party risk management?

Because an independent qualified third party performs the audit annually, it gives quality and procurement teams a defensible, repeatable basis for trusting Oracle as a critical cloud vendor — reinforcing your broader third-party risk management program.

Ready to reduce your validation burden? Contact USDM to learn more about USDM Cloud Assurance™ for Oracle SCM Cloud and discover the least burdensome approach for your needs.


[1] General Principles of Software Validation; Final Guidance for Industry and FDA Staff, FDA (2002).

Ready to act on this?

Map the next practical step with USDM.

USDM can help translate the article topic into a defensible plan for your systems, teams, and regulatory context.

Explore capabilities

Find the USDM practice area most relevant to this topic.

Platform partners

See how USDM delivers outcomes on the platforms you use.

Related resources

Keep exploring

Hand-picked blogs, case studies, and guides on the same topic.

Blog

Validating SharePoint for Life Sciences Regulated Environments

Learn how to validate SharePoint for GxP-regulated life sciences environments — from scoping intended use to qualifying security, audit trails, versioning, and workflows so SharePoint can serve as a compliant EDMS or quality management system.

Read
Webinar

Update from the FDA on CSV Changes

Watch this on-demand webinar with the FDA's Francisco Vicenty and USDM's Sandy Hedberg to understand the shift from Computer System Validation (CSV) to the risk-based Computer Software Assurance (CSA) approach — and how to apply it to your regulated systems today.

Read
White Paper

Google Cloud Platform for Life Sciences and Health Technology

A white paper on building secure, inspection-ready Google Cloud programs for life sciences — aligning GxP controls, identity and access, data governance, DevOps evidence, and USDM Cloud Assurance from the start.

Read
Webinar

USDM Life Sciences Summit 2026

Watch the 2026 USDM Life Sciences Summit on-demand to learn how to accelerate digital trust, adopt AI safely in GxP operations, modernize TPRM and cybersecurity, and enable the next-gen regulated workforce.

Read
Blog

Lessons in Cloud Assurance

Lessons in cloud assurance for life sciences: vendor qualification, GxP cloud validation, change control cadence, and continuous compliance with CSA.

Read
Blog

Q&A: How to Maximize Your GxP Use of the Public Cloud

Expert answers from USDM's webinar on running GxP workloads in the public cloud: multi-cloud strategy, the Unify Public Cloud (UPC) methodology, validation, SDLC and Agile, RPA vs. AI, and leveraging SaaS vendor documentation while staying continuously compliant.

Read
Blog

Top 10 Recurring Audit Observations at Life Sciences Companies

USDM auditors share the 10 recurring audit observations they see most often at pharma, biotech, and medical device companies — from environmental monitoring gaps to supplier qualification and cleaning validation — and how to close them before an inspector does.

Read