Specifications

Example Definitions of "Specifications"
Specifications. Any protocols, procedures, process parameters, analytical tests and other specifications for the Services and Deliverables included in the Development Plan
Specifications. The manufacturing instructions, test methods, raw materiel specifications, In-process specifications, and Product specifications as provided by CytRx to NA from time to time.
Specifications. Shall mean the specifications, performance standards and other descriptions of the Technology set forth on Exhibit A attached hereto.
Specifications. The specifications for the Antibodies set out in Schedule 1, as they may from time to time be amended pursuant to the terms of this Agreement.
Specifications. Means the design, functional, technical, scientific, packaging and other specifications of the Products set out in the applicable "Deveice Master Record and for reference set out in Appendix I hereto, which may from time to time be modified in accordance with this Agreement (including, without limitation, Section 14 hereof).
Specifications. The applicable testing specifications, such as sensitivity, specificity and sample type for the EGFR Assay and/or IVD as mutually agreed upon by the Parties based on the outcome of the Feasibility Study.
Specifications. The description of and specifications for Supplied API described on Exhibit A, attached hereto, and shall include the Cempra Specifications, all of which may be further amended by the parties according to the terms hereof
Specifications. Are the final Product release specifications as defined in Exhibit A, as amended by the Parties in accordance with this Agreement.
Specifications. Means the specifications of the Product as set out in Appendix 1 (as may be amended from time to time pursuant to Section 2.4 below) and as filed with and approved by the Relevant Authorities;
Specifications. The specifications of the Product as set out in Appendix 1 (as may be amended from time to time pursuant to Section 2.4 below) and as filed with and approved by the FDA and/or any other Relevant Authorities, together with the manner of performance of the Manufacturing Services and specification of the related Raw Materials, components, methods and stability protocols and procedures as set forth in and in accordance with (a) the relevant Marketing Authorization, (b) the master control documents... and change control documents utilized as of the Effective Date, as may be amended from time to time upon written agreement of the Parties, and (c) cGMPs View More
All Definitions