Material Review Board definition

Material Review Board or “MRB” means a group of specialists from Buyer’s quality and engineering departments formally constituted, under the coordination of the quality department, whose function is to review, evaluate, determine the disposition of nonconforming material, and request corrective actions;
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Material Review Board or “MRB” means any mutual board, committee, or other group authorized to review and approve materials used in the Products.
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Material Review Board. Leads MRB meetings related to supplier quality problems. Participate in discrepant material reviews for issues caused by Xxxxx. • New Product Qualification: Leads and participates in quality related new product development requirements as defined in Reell’s phase gate PDP process. Provide support for design quality assurance requirements. • Receiving Inspection: Manages requirements for receiving inspection when component parts are de- certified. Assure supplier quality requirements are implemented to avoid the need for receiving inspection. Work closely with inspector(s) as needed if the need arises to verify de-certified components. • Process Audits: Develops and implements an effective supplier quality auditing process for off-site and on-site audits. Work closely with other Reell coworkers and contract manufacturing partners in assuring supplier quality audits are effective.
Sample 1

Examples of Material Review Board in a sentence

  • Makes a preliminary determination from work orders, drawings and inspection documentation as to whether such items are scrap or for referral to the Material Review Board.

  • Reviews production standards and Functional Test Procedures for correct inclusion of Quality System requirements; may act as an authorized Quality representative on the Material Review Board (MRB).

  • Inspection Mechanic A* = can be assigned to any and all inspection tasks including Material Review Board (MRB) disposition approval and First Article Inspection (FAI) where qualified and holding appropriate certifications.

  • In those cases where Seller has a Material Review Board (MRB), a statement of whether Seller’s proposed Component Escape correction meets type design or a separate submission establishing why a full review by MRB for the Component Escape is not necessary.

  • Material Review Board (MRB) authority is not delegated to the Seller.

  • In those cases where Seller has a Material Review Board (MRB), a statement of whether Xxxxxx’s proposed Component Escape correction meets type design or a separate submission establishing why a full review by MRB for the Component Escape is not necessary.

  • For Seller’s catalog and standard products, Seller shall maintain Material Review Board (MRB) authority and reserves the right to make changes to parts, materials, processes, testing methods and place of manufacture without prior notice to Buyer.

  • Parts subject to subsequent processing not authorized by specification shall be submitted to Ophir Corporation Material Review Board for authorization.

  • Unless otherwise specified in this Purchase Order, the Supplier and/or any of their Suppliers/Subcontractors DO NOT have authority to process “USE-AS-IS”, “REPAIR”, “STANDARD REPAIR PROCEDURES (SRPS)” or “NON-SRPS” via their Material Review Board (MRB).

  • BUYER or their customer retains Material Review Board authority over contract specifications.


More Definitions of Material Review Board

Material Review Board or “MRB” means a group of specialists from Buyer’s quality and engineering departments formally constituted, under the coordination of the quality department, whose function is to review, evaluate, determine the disposition of nonconforming material, and request corrective actions; 1.1.38 “Obsolescence” means the discontinuation of desirability, availability and/or usefulness of a Component in the production or support of the Aircraft and/ or its related Components and systems caused by new inventions, technological evolution, changes in design, improvement of production processes or external factors such as regulatory issues and environmental restrictions; 1.1.39 “OEM” means Original Equipment Manufacturer; 1.1.40 “Other Program Participants” or “OPP” means any third party responsible for a function or for a supply of Aircraft parts or Components for the Program; 1.1.41 “Parties” mean Buyer and Supplier, taken collectively; 1.1.42 “Party” means each of Buyer and Supplier, individually; 1.1.43 “Piece Part” means a subassembly or discreet Component used in production, maintenance and Correction in support of LRUs and LRMs; 1.1.44 “Preliminary Design Review” or “PDR” means the event in which is performed a preliminary design review assessment to verify that the proposed Product design meets the functional and performance requirements and all the interfaces among Supplier’s Products, OPP’s Products and the Aircraft are proper defined to proceed with the detailed design, as further detailed in the Exhibit I; 1.1.45 “Price” means the total amount paid by Buyer to Supplier in accordance with Section 3.2 of this Agreement; 1.1.46 “Product” means all goods, including Piece Parts, software, parts and/or Components, GSE thereof for the Aircraft (including any prototype Aircraft) and/or for any simulator, as well as Technical Publications, certificates of conformance (CofC), and any other Product documentation, to be provided by Supplier under this Agreement, as further described in the Exhibits attached hereto, as may be amended from time to time and include those goods provided by the Supplier under this Agreement which are intended for Buyer Group’s use, Customer’s use, or for sale as Spare Parts or production replacements; 1.1.47 “Program” means all activities related to the design, development, certification, manufacturing, sales and after-sales support of the Aircraft including, but not limited to Customer Support;
Sample 1
Material Review Board. (MRB) means a Cubist multidisciplinary committee responsible for the review, evaluation and disposition of non-conforming materials and Product. NDA means a new drug application filed with the FDA to obtain marketing approval for Product in the United States or any comparable application fled with the regulatory authorities of a country other than the United States to obtain marketing approval for Product in that country.
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Material Review Board means any internal board, committee, or other group of Filtertek employees authorized to review and approve raw materials used in the Products (excluding, in the case of approval, with respect to the HemaSure Materials).
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Material Review Board means a committee that reviews deviations and out of specification results for Raw Materials, in-process materials and API, and determines the actions needed to investigate the deviation, the corrective/preventive action, and disposition of the product. The MRB is composed of management representatives from Quality Assurance, Quality Control, and Manufacturing.
Sample 1
Material Review Board. Leads MRB meetings related to supplier quality problems. Participate in discrepant material reviews for issues caused by Xxxxx. • Receiving Inspection: Manages requirements for receiving inspection when component parts are de- certified. Ensure supplier quality requirements are implemented to avoid the need for receiving inspection. Work closely with inspector(s) as needed if the need arises to verify de-certified components. • Process Audits: Develops and implements an effective supplier quality auditing process for off-site and on-site audits. Work closely with other Reell coworkers and contract manufacturing partners in ensuring supplier quality audits are effective. • QCDS: Develops metrics and systems to ensure quality improvements. Improve customer confidence in Xxxxx’s product quality. Develop plans and follow-thru on continuous improvement in supplier quality and customer satisfaction. Drive efficiency gains by utilizing various methodologies such as kaizen events, Lean-Sigma tools while effectively incorporating ideas from coworkers. Develop and monitor performance metrics in quality, cost, delivery and safety (QCDS). • Other duties as required.
Sample 1

Related to Material Review Board

  • Institutional Review Board or “IRB” means, in accordance with 45 C.F.R. Part 46, 21 C.F.R. part 56, and other applicable regulations, an independent body comprising medical, scientific, and nonscientific members, whose responsibility is to ensure the protection of the rights, safety, and well-being of the Human Subjects involved in a study.

  • Review Board has the meaning provided in Section 2.1(f)(i) of this Commercial Shared-Loss Agreement.

  • Architectural Review Committee or “ARC” shall mean the architectural review committee established by the Organization to review plans submitted to the Organization for architectural review.

  • Medical Review Officer (MRO) means a licensed physician responsible for receiving and reviewing laboratory results generated by the school district’s drug testing program and for evaluating medical explanations for certain drug tests.

  • Medical Review Officer (MRO means a licensed M.D. or D.O. with knowledge of drug abuse disorders, employed or used by the City to review drug results in accordance with this procedure.

  • Supervisory Review means ongoing clinical case reviews in accordance with procedures developed by ADMINISTRATOR, to determine the appropriateness of Diagnosis and treatment and to monitor compliance to the minimum ADMINISTRATOR and Medi-Cal charting standards. Supervisory review is conducted by the program/clinic director or designee.

  • Independent review organization means an entity that is accredited to conduct independent external reviews of adverse benefit determinations.

  • independent review committee means the independent review committee of the investment fund established under National Instrument 81-107 Independent Review Committee for Investment Funds;

  • New Board means the board of directors or the board of managers of Reorganized Neiman.

  • Peer review committee means one or more persons acting in a peer review capacity who also serve as an officer, director, trustee, agent, or member of any of the following:

  • Annual Review means the process as set out in Clause 2.2 below and refers to the annual process of reviewing information and provisions of this Agreement in the light of legal and other changes at the School or the payment history of the parent/guardian. This is known as re- registration.

  • Ethics Committee means an independent body established in a Member State in accordance with the law of that Member State and empowered to give opinions for the purposes of this Regulation, taking into account the views of laypersons, in particular patients or patients' organisations;

  • Clinical review criteria means the written screening procedures, decision abstracts, clinical protocols, and practice guidelines used by a health carrier to determine the necessity and appropriateness of health care services.

  • Prospective review means utilization review conducted prior to an admission or a course of treatment.

  • Division board means the board of the title guaranty division created pursuant to Iowa Code section 16.2A(1).

  • Expedited review means an examination, in accordance with

  • Utilization review organization means an entity that conducts utilization review, other than a health carrier performing a review for its own health benefit plans.

  • Benchmark Review means a review of the Services carried out in accordance with paragraphs 2.1 to 2.3 of Schedule 7 (Value for Money) of this Framework Agreement to determine whether those Services represent Good Value;

  • LOCAL BOARD OF TAX REVIEW and "BOARD OF TAX REVIEW" means the entity created under Section 182.18 of this Chapter.

  • Medical Board means the North Carolina Medical Board.

  • Grievance Committee means the Grievance Committee of the Bar.

  • College board means the state board for community and

  • New Boards means, collectively: (a) the Reorganized TCEH Board; and (b) the New EFH/EFIH Board.

  • Quality improvement organization or “QIO” shall mean the organization that performs medical peer review of Medicaid claims, including review of validity of hospital diagnosis and procedure coding information; completeness, adequacy and quality of care; appropriateness of admission, discharge and transfer; and appropriateness of prospective payment outlier cases. These activities undertaken by the QIO may be included in a contractual relationship with the Iowa Medicaid enterprise.

  • Supervisory Committee means the Comisión Fiscalizadora of the Company.

  • Supervisor means Advisors Asset Management Inc., and its successors in interest, or any successor evaluator appointed as hereinafter provided."