In aerospace, a small defect can become a large decision. A burr, porosity indication, missing certificate, corrosion finding, or dimensional deviation can affect safety, delivery, cost, and configuration control. That is why mrb aerospace processes need clear authority, disciplined evidence, and traceable execution.Overview: What Is an Aerospace Material Review Board (MRB)?A material review board is…

In aerospace, a small defect can become a large decision. A burr, porosity indication, missing certificate, corrosion finding, or dimensional deviation can affect safety, delivery, cost, and configuration control. That is why mrb aerospace processes need clear authority, disciplined evidence, and traceable execution.
A material review board is a controlled authority for evaluating nonconforming material, components, assemblies, raw materials, and records. A Material Review Board (MRB) is a cross-functional team that evaluates nonconforming materials to determine their fate, ensuring decisions are based on quality and safety considerations.
The material review board MRB is not just a meeting held on a weekly or monthly basis. It is a material review board process embedded in daily operations across OEMs, Tier 1 suppliers, and MRO organizations. It connects the non conformity report, concessions, deviations, engineering analysis, production data, and final disposition.
Do not confuse this with the Maintenance Review Board (MRB), which governs scheduled fleet-wide maintenance standards in aviation, playing a critical role in maintaining airworthiness. The aerospace material review function focuses on product nonconformance and whether the affected item can move forward.
AS9100 and regulatory expectations require nonconforming product to be identified, reviewed, approved, and documented by authorized personnel. FAA guidance such as FAA Order 8120.23 reinforces the need for defined MRB authority and objective records.
Connect 981 supports this work by tying ERP, MES, QMS, supplier, and shopfloor data into one traceable mrb process, so the current mrb record is not scattered across emails or shared folders.

An MRB must consist of highly specialized subject matter experts, including stress engineers, quality assurance specialists, and design engineers. The board members usually come from different departments because one function rarely has enough context to decide alone.
Typical roles include:
Authority is delegated through a charter, quality manual, customer agreement, or engineering authority letter. Local boards may decide minor issues. Major or safety-critical deviations often require OEM, customer, FAA, or EASA approval. MRB teams are responsible for keeping manufacturing and production lines running smoothly while adhering to stringent structural and airworthiness standards, but they must still challenge schedule pressure when conformity or safety is at risk.
The MRB process typically begins with the creation of a Nonconformance Report (NCR) when a defect is identified, which is then reviewed by the board to decide on the appropriate disposition of the nonconforming materials.
In Connect 981, this flow is captured in one controlled record, visible to quality, engineering, production, procurement, and suppliers.
Common dispositions made by the MRB include accepting materials as-is, reworking them, returning them to the vendor, or scrapping them if they cannot be corrected. The Material Review Board (MRB) can recommend several dispositions for nonconforming materials, including use as-is, rework, return to vendor, and scrap.
Every disposition needs rationale, risk level, required follow-up, and approval trace.
Each mrb record should include NCR number, part number, serial or lot number, work order, affected aircraft or engine registration for MRO, defect description, detection point, responsible organization, drawings, specifications, and revision levels.
Evidence includes inspection reports, NDT images, measurement data, supplier certificates, photos, test logs, stress calculations, and engineering approvals. Effective MRB practices require that all decisions regarding nonconforming materials are defensible, meaning that the rationale for each decision must be recorded contemporaneously and linked to objective evidence, ensuring compliance with regulatory standards.
Traceability must run backward to materials, suppliers, processes, and approved data, and forward to affected assemblies, aircraft, customers, and as-maintained configuration.
Regulatory requirements mandate that nonconformances are investigated, decisions are justified, and records are complete, particularly in industries such as pharmaceuticals and medical devices, which are governed by 21 CFR regulations. The Material Review Board (MRB) process must integrate with quality management systems to ensure that all decisions regarding nonconforming materials are documented with objective evidence, including e-signatures and secure audit trails, as required by regulations like Part 11 and Annex 11.
Compliance gaps can arise when MRB documentation is inconsistent, leading to audits being complicated by missing approvals or unclear records.
MRB is part of the broader quality system, not a separate island. NCRs identify and document the condition. MRB decides the disposition. CAPA addresses why the issue happened and how to prevent recurrence.
MRB teams contribute to aviation safety by maintaining structural integrity and preventing future failures through root cause analysis. Repeated material review cases may trigger supplier 8D, process changes, updated inspection plans, or engineering change notices. If the same deviation is discussed every monthly basis, the issue is no longer just an MRB workload problem. It is a system signal.
Connect 981 links NCR, MRB, CAPA, and change workflows so leaders can see whether corrective action reduces future risk.
Disconnected data and documentation can slow down MRB processes, as many reviews still rely on spreadsheets or shared folders, leading to confusion about the most current information. Manual routing and follow-up can stall MRB processes, as reliance on people passing forms or forwarding emails can lead to delays if someone is unavailable.
Digital MRB changes the control point. On-hold parts cannot be issued, installed, or shipped until an approved mrb decision is complete. Role-based access ensures only authorized board members approve dispositions. E-signatures, timestamps, and revision history create the audit trail.
Limited visibility into patterns of nonconformance can hinder MRB effectiveness, as data scattered across drives makes it difficult to identify recurring issues before they escalate. Dashboards for open cases, scrap value, supplier trends, and cycle time help most manufacturers focus improvement work where it matters.

Connect 981 is an aerospace operations platform that unifies NCRs, MRB decisions, CAPA, routing, supplier workflows, and work execution on top of existing ERP, MES, PLM, and QMS systems.
Zero and low-code tools let quality and manufacturing engineers configure approvals, notifications, and templates without a long IT project. Digital work instructions execute rework and repair consistently, while results and signoffs are captured at the point of work.
For teams modernizing mrb aerospace processes, the goal is practical: stronger disposition control, clearer decision authority, and audit-ready traceability. Request a Connect 981 demo to see how your MRB workflow can be standardized across sites and suppliers.
Whether you're managing 1 site or 100, Connect 981 adapts to your environment and scales with your needs—without the complexity of traditional systems.