Quality Controls. Management Company shall activate and maintain on a continuing basis, a quality assurance program which provides objective measurements of the quality of services provided at the Facility. In connection therewith, Management Company shall utilize such techniques (e.g. resident interviews and periodic inspections) as Management Company may reasonably deem necessary to maintain the quality of the Facility.
Quality Controls. Manager shall activate and maintain on a continuing basis a "Quality Assurance Program" in order to provide objective measurements of the quality of health care provided at the Facility and, in connection therewith, shall utilize such techniques as patient questionnaires and interviews, physician questionnaires and interviews, and inspections.
Quality Controls. The Company shall comply with the Quality Control Plan dated August 1, 2008, a copy of which has been delivered to the Buyer (the “Quality Control Plan”), in accordance with its terms.
Quality Controls. Both Parties shall institute quality controls in accordance with, and shall comply with, applicable laws and regulations and generally accepted industry standards (including cGMPs as defined below) for the manufacture, storage, shipment, handling and distribution of the Compound, the Product and the Finished Product (as the case may be) and shall define responsibilities for key quality systems and a quality manual agreed to by both Parties (including without limitation, Sample Packs) and shall comply with all applicable laws and regulations relating to the storage, shipment, handling and distribution of the Compound, the Product and the Finished Product. Each Party shall have the right to audit all facilities used by the other Party to fulfill their obligations under this Agreement (including any Third Party manufacturing facilities). For the purposes of this Agreement, "cGMPs" means all applicable standards relating to manufacturing practices for intermediates, bulk products, or finished pharmaceutical products (i) promulgated in the form of laws or regulations by the FDA or its counterpart governmental agencies or entities in the EU and/ or a country in the International Territory or (ii) promulgated by the FDA or its counterpart governmental agencies or entities in the EU and/ or a country in the International Territory in the form of guidance documents (including but not limited to advisory opinions, compliance policy guides and guidelines) which guidance documents are being implemented within the pharmaceutical manufacturing industry for such products.
Quality Controls. Manager shall implement and maintain on a continuing basis a Quality Assurance Program at the Facility and in connection therewith shall utilize such techniques as Manager deems appropriate in order to fulfill its duties herein.
Quality Controls. 4.1 Licensee agrees to deliver samples of all materials which bear the Intellectual Property to Licensor for Licensor's approval and acceptance prior to the use of such materials by Licensee. Licensor has 5 business days to approve in writing the submitted materials. If Licensor has not notified Licensee of its disapproval in writing within 5 business days, such materials will be automatically assumed to have been approved by Licensor.
4.2 Licensee agrees not to alter, change, modify or supplement any materials bearing the Intellectual Property without Licensor's prior written consent.
4.3 Licensee acknowledges that the Intellectual Property is of substantial value to Licensor and Licensee will fully comply with the specifications, directions, and standards of quality imposed by Licensor from time to time to preserve, maintain and enhance the reputation and goodwill in the Intellectual Property developed by Licensor and its affiliates. Licensee shall ensure that all materials on which the Intellectual Property is used or associated therewith will meet all specifications, directions, and standards of quality imposed by Licensor and will satisfy in performance, quality, construction and use the reasonable requirements of Licensor and shall, upon notice from Licensor, give Licensor or its authorized representative, free access at any reasonable time to the premises of Licensee for the purpose of ensuring that Licensee is observing these obligations.
4.4 Should Licensor notify Licensee that any use of the Intellectual Property fails to comply with Licensor's specifications, directions or standards of quality for such use, Licensee shall promptly proceed to correct any defects in accordance with instructions from Licensor. Failure to correct such defects will result in the termination of this Agreement.
4.5 All use of the Intellectual Property by Licensee and its affiliates shall conform with proper practices, as applicable. Licensee shall take all reasonable actions to assist Licensor in protecting the Intellectual Property.
4.6 Licensee shall use the Intellectual Property in the form stipulated by Licensor and shall observe any reasonable directions given by Licensor as to colors and sizes of the representations of the Intellectual Property and their manner and disposition.
4.7 All material on or in relation to which Licensee proposes to use the Intellectual Property shall bear a legible statement that identifies Licensor as the owner of the Intellectual Prop...
Quality Controls. Licensor shall have the right to and shall control the nature and quality of Licensed Product. Licensor shall work with Licensee with respect to the manufacture of the Licensed Products. Licensee shall not manufacture or sell the Licensed Products until Licensor has given its approval in writing, for the Licensed Products. Such approval shall be in a timely manner and not unreasonably withheld. In addition, to assure itself that the Licensed Product as sold by Licensee complies with Licensor’s specifications and quality standards, including Statement of Work, upon reasonable notice, Licensor shall have the right at all reasonable times during normal business hours to inspect the Licensed Products and to inspect the facilities and the methods of manufacturing the same; and, at its cost, Licensee shall send to Licensor or through its designated representative, reasonable quantities of random production samples of the first production run of the Licensed Products and thereafter shall send random production samples as Licensor may reasonably request from time to time. Licensee shall correct to Licensor’s satisfaction any deficiencies in the nature or quality of the Licensed Products according to instructions provided by Licensor.
Quality Controls. WE have established quality controls and procedures which WE try to enforce, but human and technical means of review are not perfect. In spite of this, WE are committed to ensuring that electronic files of all content on the Web Site are valid NIMAS files. However, due to the inherent technological limitations, WE cannot and do not guarantee that there are no errors in the Files or the content contained therein. WE, therefore, do not guarantee the quality or accuracy of any information or content provided on the Web Site.
Quality Controls. Both Parties shall institute quality controls in accordance with generally accepted industry standards for the storage, shipment, handling and distribution of the Products and shall define responsibilities for key quality systems and a quality manual agreed to by both Parties (including without limitation, Sample Packs) and shall comply with all Legal Requirements relating to the storage, shipment, handling and distribution of the Products. Triangle and Xxxxxx shall institute quality controls in accordance with generally accepted industry standards for the manufacture of Products. Each Party shall have the right to audit all facilities used by the other Party to fulfill their obligations under this Agreement (including any Third Party manufacturing facilities, in accordance with the terms of the underlying manufacturing agreement).
Quality Controls. Both Parties shall institute quality controls in accordance with, and shall comply with, applicable laws and regulations and generally accepted industry standards (including CGMPs as defined below) for the manufacture, storage, shipment, handling and distribution of the Compound, the Product and the Finished Product (as the case may be) and shall define responsibilities for key quality systems and a quality manual agreed to by both Parties (including without limitation, Sample Packs) and shall comply with all applicable laws and regulations relating to the storage, shipment, handling and distribution of the Compound, the Product and the Finished Product. Each Party shall have the right to audit all facilities used by the other Party to fulfill their obligations under this Agreement (including any Third Party manufacturing facilities). For the purposes of this Agreement, "
