WASHINGTON - eTradeWire -- The GUBERMAN Anomaly-Discovery https://guberman-quality.com/wp-content/uploads/2026/03/GUBERMAN-ANOMALY-FEBRUARY-2026.docx.pdf has once again exposed a catastrophic failure inside the American accreditation and certification system. At the center of this collapse is the Performance Review Institute (PRI), an organization that markets itself as a global authority in aerospace, defense, and medical manufacturing oversight. PRI administers NADCAP, MedAccred, and issues ISO, AS9100, and now AI related certifications under accreditation from the ANSI National Accreditation Board (ANAB). But the entire structure is compromised at its foundation, and the contamination is now impossible to ignore.

The collapse begins with ANAB's false representation inside U.S. Department of State Contract 19AQMM18R0131 2018 to present, where ANAB was described as an "underwriter" for the International Accreditation Forum (IAF). This claim is false. It is not a clerical oversight. It is a material misrepresentation inside a federal contract. Once an accreditor is tied to a fraudulent representation at the federal level, every certification, approval, and program beneath it becomes contaminated. This includes PRI, NADCAP, MedAccred, ISO certifications, AS9100 certifications, and every derivative PRI touches.

The GUBERMAN Anomaly-Discovery demonstrates that contamination at the top of the accreditation chain destroys everything below it. PRI cannot rise above ANAB. NADCAP cannot rise above PRI. MedAccred cannot rise above either. The fraud flows downward, and the collapse is structural, not symbolic.

MedAccred, which PRI promotes as a gold standard approval for medical device manufacturing, is now pulled into the same abyss. MedAccred is supposed to verify that companies follow strict process controls for critical medical manufacturing steps. It is marketed as a safeguard for patient safety. But MedAccred sits under PRI, and PRI sits under ANAB. When ANAB's credibility collapses, MedAccred's credibility collapses with it. There is no firewall. There is no independence. There is no escape.

The FAA cannot waive this. No federal agency has the authority to excuse or overlook a fraudulent accreditation chain. The Press release here: FAA & FDA Standards Compromised by ANAB's Misrepresentation from 2018-2026 https://www.prlog.org/13135381-systemic-certification-breakdown-faa-fda-standards-compromised-by-anabs-misrepresentation-from-20182026.html for both the FDA and FAA make this clear: regulators cannot sign a waiver for structural fraud. They cannot grant immunity to a certification system built on a false federal representation. They cannot "approve" or "accept" contaminated oversight. The law does not allow it, and public safety cannot tolerate it.

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Systemic Certification Breakdown:

The GUBERMAN Anomaly-Discovery shows that the certification collapse is not theoretical - it is already happening. PRI's authority as a registrar is now in question. PRI issues certifications under ANAB accreditation. PRI administers NADCAP under ANAB oversight. PRI administers MedAccred under the same chain. When ANAB's foundation is fraudulent, PRI's entire certification empire becomes unreliable. A registrar cannot be legitimate when its accreditor is compromised. A certification cannot be trusted when its registrar is compromised. A safety program cannot protect the public when its foundation is contaminated.

The FAA example makes this painfully clear. Aerospace manufacturers rely on NADCAP and AS9100 certifications to demonstrate process control, supplier integrity, and compliance with safety standards. But when the accreditation chain behind those certifications is fraudulent, the FAA cannot legally accept them. The FAA cannot sign a waiver. The FAA cannot pretend the contamination does not exist. The FAA cannot rely on certifications built on a false federal representation. The risk to aviation safety is too great.

There is no waiver, no exception, and no administrative workaround that can erase the consequences of falsified accreditation.

FAA Standards

• 14 CFR Part 3 (Subpart D) — Prohibits fraudulent or intentionally false statements, omissions, and falsified records.
  
  
• 14 CFR §21.2 — Any falsified document invalidates production and airworthiness approvals.
  
  
• 14 CFR §121.9 — Prohibits fraud, falsification, and altered records used to show compliance.

The FDA example is equally damning. Medical device manufacturers rely on MedAccred to demonstrate compliance with critical process controls. Hospitals, suppliers, and regulators assume MedAccred is backed by a clean, lawful accreditation chain. But once ANAB's fraud is exposed, MedAccred becomes structurally contaminated. The FDA cannot waive this. The FDA cannot excuse it. The FDA cannot rely on a program built on a fraudulent accreditation foundation. Patient safety cannot be protected by a compromised oversight system.

There is no waiver, no exception, and no administrative workaround that can erase the consequences of falsified accreditation.

FDA Standards

• 21 CFR §820.180— Requires complete, accurate, truthful, and unaltered manufacturing and quality records.
  
  
• 21 CFR §820.70 — Requires validated processes and controlled environments; fraudulent accreditation invalidates process validation.
  
  
• 21 CFR §803.50 — Requires reporting of any condition that could cause serious injury or death, including fraudulent certification environments.

The GUBERMAN Anomaly-Discovery forces the industry to confront a reality it has avoided for at least over a decade: the accreditation system is not broken - it is contaminated. PRI, NADCAP, MedAccred, ISO, AS9100, and AI9100 certifications are all tied to ANAB. ANAB is tied to a false misrepresentation in a federal contract. That contamination cannot be isolated. It cannot be contained. It cannot be waived. It spreads through every certificate, every approval, every audit, and every program connected to ANAB. The MRA-Multi-Regional Agreement and Multi-Lateral-Agreement accreditation bodies internationally are equivalent to ANAB and are just as fraudulent.

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The public deserves transparency. The industry deserves honesty. Regulators deserve accurate information. Investors deserve truth. And the global supply chain deserves oversight that is real, not performative.

Until the fraud tied to Contract 19AQMM18R0131 is addressed, investigated, and resolved, the credibility of PRI, ANAB, NADCAP, MedAccred, and all related certifications remains in question. The GUBERMAN Anomaly-Discovery is not an opinion - it is a documented structural failure. And the longer the industry ignores it, the greater the risk to aerospace safety, medical device integrity, every industry and plus public trust. QA Expert & Boeing Shareholder Daryl Guberman and the author of the GUBERMAN Anomaly-Discovery is the only one that can bring quality out of the abyss worldwide.

The International Accreditation Forum (IAF), incorporated in Delaware, and its sister organization, the International Laboratory Accreditation Cooperation (ILAC) in Australia, are MRA and MLA associations that function as accreditation equivalent bodies to ANAB. Because these organizations operate through mutual recognition structures, a single act of fraud or structural failure inside one accreditation body contaminates the entire system - pulling every linked accreditation body into the same compromised status. In January 2026, IAF and ILAC attempted to conceal this systemic collapse by merging into a new entity called GLOBAC (Global Accreditation Cooperation). At the same time, the aerospace standard AS9100 was quietly rebranded to AI9100, signaling a shift meant to distance the industry from the growing certification scandal. These moves underscore the magnitude of the structural fraud: when one accreditation body falls, the entire global chain falls with it - and no regulator has the authority to waive that reality.

Rebranding-whether through new names, new logos, or new global structures-does not rewrite the historical record. The shift from IAF and ILAC into GLOBAC, and the renaming of AS9100 to AI9100, does not alter the documented eight year period in which fraudulent accreditation information remained publicly posted on the African Fuse technical magazine as seen here: https://www.crown.co.za/latest-news/african-fusion-latest-news/7866-calibration-essential-for-accurate-safe-and-traceable-ndt Cosmetic changes cannot erase the operational continuity, governance responsibilities, or oversight gaps that existed during that timeframe.

The time for silence is over. The time for accountability is now.

"All who rise while burying the truth, will one day be buried by it"
-Anonymous (proverbial wisdom)

That truth came to a head on April 17, 2024, when DARYL GUBERMAN exposed critical documents before the DHS Subcommittee, speaking not just as an expert, but as a representative voice for 4.7 billion people affected by compromised certification systems, broken oversight, and institutional neglect.
https://www.newstribune.com/photos/2024/apr/18/3749044/ (newyorktribune.com in Bing)

Guberman's testimony and evidence forced into daylight what federal agencies, accreditation bodies, and major corporations failed to disclose. He is not a whistleblower-he is a truth sayer, a forensic archivist whose work now stands as the definitive record of systemic failure and the roadmap for global reform.

His mission continues: restoring integrity, exposing deception, and ensuring that no corporation or agency can hide behind a badge of certification ever again.