Product Review definition

Product Review shall have the meaning ascribed to it in Clause 5a(i); “Promotional Materials” shall have the meaning ascribed to it in Clause 4h; “Rectification Period” shall have the meaning ascribed to it in Clause 9b(iii). “Remedial Period” shall have the meaning ascribed to it in Clause 5g.
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Product Review has the meaning set forth in Section 4.5(a).
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Product Review means ADEQ verification that a product used in an onsite wastewater treatment facility will signif- icantly affect treatment performance or provide the means to overcome site limitations.
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Examples of Product Review in a sentence

  • OGS reserves the right to unilaterally make revisions, changes, additions and/or updates to the ‘How to Use’ and ‘Request for Product Review (RFPR) Template’ without processing a formal amendment and/or modification.

  • The Contractor will not charge an insurance company being examined for work under this Contract.The Contractor will carry out this project under the direction and control of:Randy Parlor, Director Product Review SectionOffice of Financial and Insurance RegulationMichigan Department of Energy, Labor & Economic Growth 611 W.

  • Licensing and Product Review Division: Property/Casualty Rate Review Actuarial ServicesWhen specific company rate reviews require actuarial services, the OFIR Program Manager will prepare a written work statement detailing the work to be performed by the Contractor.

  • Authorized Users should refer to Attachment 4 How to Use and Attachment 6 Request for Product Review (RFPR) Template for specific procurement instructions.

  • At the Client’s request, Patheon will provide a copy of the Annual Product Review Report to the Client at no additional cost.

  • Emergency Use Authorization (EUA) for an Unapproved Product Review Memorandum.

  • Additional requirements for Product Review submittals are contained in the Technical Specification sections.

  • The committee may research and make recommendations for safer substitutes or modifications to the new equipment, medical treatments and/or processes to the Product Review Analysis Committee.

  • But for all to read, share and remember; an ultra righteous racist by the name of S.Tan, I have decided to post it here.

  • The Contractor shall make all Product Review submittals early enough to allow adequate time for the Engineer's review, for manufacture and for delivery at the construction site without causing delay to the Work.


More Definitions of Product Review

Product Review shall have the meaning ascribed to it in Clause 5a(i);
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Related to Product Review

  • Batch means a specific quantity of Product that is intended to have uniform character and quality, within specified limits, and is produced according to a single manufacturing order during the same cycle of manufacture.

  • Product Schedule means PTC’s standard order form entitled “PTC Product Schedule” (including all schedules, attachments and other document(s) specifically referenced therein) or such alternative order form as may be submitted by Customer and accepted by PTC, in each case that specifies (i) the Licensed Products and/or Services ordered; and (ii) for Licensed Products, the installation address (including the Designated Country) and the Licence Term.

  • Product Complaint means any written, verbal or electronic expression of dissatisfaction regarding the Product, including without limitation reports of actual or suspected product tampering, contamination, mislabeling or inclusion of improper ingredients.

  • Product means any deliverable under the Contract, which may include commodities, services, technology or software.

  • 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;

  • Drug sample means a unit of a prescription drug that is not intended to be sold and is intended to promote the sale of the drug.

  • Application Review Start Date means the later date of either the date on which the District issues its written notice that the Applicant has submitted a completed Application or the date on which the Comptroller issues its written notice that the Applicant has submitted a completed Application and as further identified in Section 2.3.A of this Agreement.

  • Peer review means evaluation of professional services rendered by a professional practitioner.

  • Product Labeling means, with respect to a Licensed Product in a country or other jurisdiction in the Territory, (a) the Regulatory Authority-approved full prescribing information for such Licensed Product for such country or other jurisdiction, including any required patient information, and (b) all labels and other written, printed, or graphic matter upon a container, wrapper, or any package insert utilized with or for such Licensed Product in such country or other jurisdiction.

  • Finished Product means a cannabis product in its final form to be sold at a retail premises.

  • Investigational Product means the Study Drug identified above and the control material, as further detailed in the Protocol;

  • Diagnostic clinical procedures manual means a collection of written procedures that describes each method (and other instructions and precautions) by which the licensee performs diagnostic clinical procedures; where each diagnostic clinical procedure has been approved by the authorized user and includes the radiopharmaceutical, dosage, and route of administration.

  • Product Backlog means a list of those Stories that do not form part of the current Sprint Plan at that time and which are to form the subject of a future Sprint, either in the current Release at that time or a subsequent Release;

  • Drug utilization review means an evaluation of a prescription drug order and patient records for

  • Utilization review means the prospective (prior to), concurrent (during) or retrospective (after) review of any service to determine whether such service was properly authorized, constitutes a medically necessary service for purposes of benefit payment, and is a covered healthcare service under this plan. WE, US, and OUR means Blue Cross & Blue Shield of Rhode Island. WE, US, or OUR will have the same meaning whether italicized or not. YOU and YOUR means the subscriber or member enrolled for coverage under this agreement. YOU and YOUR will have the same meaning whether italicized or not.

  • Product Manufacturer means the entity that assembles the component parts to manufacture the final Product;

  • Periodic Review means a review conducted by Ofwat for the purpose of determining one or more Price Controls in accordance with Part III of Condition B, but so that references in Part IV of Condition B to a Periodic Review shall exclude any review carried out under paragraph 11 of that Condition and shall include the determination by the Competition and Markets Authority of the relevant questions or, as the case may be, the disputed determination referred to it under paragraph 16 of Condition B;

  • Manufacturing site means the facilities where a Compound is Manufactured by or on behalf of a Party, as such Manufacturing Site may change from time to time in accordance with Section 8.7.

  • Utilization review plan or "plan" means a written procedure for performing review.

  • Recall campaign means the period of time beginning on the

  • Peer-reviewed medical literature means a scientific study published only after having been critically

  • Product Specification means a product specification for a Medical Device set out in Schedule 2;

  • Drug Substance means an active ingredient that is intended to furnish pharmacological activity or other direct effect in the diagnosis, cure, mitigation, treatment, or prevention of disease or to affect the structure or any function of the human body, but does not include intermediates used in the synthesis of such ingredient.

  • Manufacturing Services means the manufacturing, quality control, quality assurance, stability testing, packaging, and related services, as set forth in this Agreement, required to manufacture Product or Products using the Active Materials, Components, and Xxxx Back Items;

  • Quality Assurance Program means the overall quality program and associated activities including the Department’s Quality Assurance, Design-Builder Quality Control, the Contract’s quality requirements for design and construction to assure compliance with Department Specifications and procedures.

  • 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.