Quality Information definition

Quality Information used herein means any information provided by any distributor, any person who directly handles the Product at customs, pharmacies, hospitals and clinics, any patient, or any other user concerning quality defects of the Product, including concerns about quality defects, after the release of the Products to the market in the Territory by The Distributor. ​
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Quality Information means any of the following: (a) CQMs including those used in connection with government initiatives; (b) claims-based quality data; (c) Supplemental Clinical Data Files used to calculate HEDIS measures; (d) HEDIS measures; or (e) quality measures and the data used to calculate them for any quality measure set.
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Quality Information means quality information relating in any way to the Manufacture of the Products, and to the use of any equipment and techniques relating to the Products, including any such information provided by Sol-Gel to ▇▇▇▇▇▇▇ prior to the Commencement Date and any such information that may be further provided by the Customer, or by Sol-Gel at the Customer’s request, to ▇▇▇▇▇▇▇ from time to time to enable ▇▇▇▇▇▇▇ to Manufacture the Products at the Facility.
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Examples of Quality Information in a sentence

  • For individuals without access to the Internet, federal agencies with Indoor Air Quality information include the EPA’s Indoor Air Quality Information Clearinghouse (IAQ INFO) at ▇.▇.

  • Regarding Faulty Products, in accordance with the Quality Information handling procedure as defined in Article 11, CASI shall investigate the cause of Faulty Products to take countermeasures and notify the result to the Distributor.

  • This publication is available at no cost from: Indoor Air Quality Information Clearinghouse ▇.▇.

  • The Surface Water Quality Information Database (SQUID) is the central repository for NMRAM data at SWQB.

  • Following an accreditation event, the LHN will provide to the Executive Director, Quality, Information and Performance: • a copy of the ‘not met’ report within two days of receipt by the LHN; • the accreditation report within seven days of receipt by the LHN, providing no significant patient risks have been identified; and • immediate advice should any requirement of a rectification period after the accreditation event not be met resulting in the facility not being accredited.

  • In advance of the Marketer Change Date, JT and GSJ will enter into a Safety Information Reporting Agreement and Quality Information Reporting Agreement, both of which will be effective during the period from the Marketer Change Date to the MAH Transfer Date.

  • This publication is available at no cost from: Indoor Air Quality Information Clearinghouse P.

  • This publication is available at no cost from: American Lung Association Environmental Health Department ▇▇▇ ▇▇▇▇ ▇▇▇▇▇▇ ▇▇▇▇▇▇▇▇▇▇, ▇▇ ▇▇▇▇▇ (800) LUNG-USA [(▇▇▇) ▇▇▇-▇▇▇▇] This publication is available at no cost from: Indoor Air Quality Information Clearinghouse ▇.▇.

  • Sol-Gel hereby grants ▇▇▇▇▇▇▇, a non-exclusive, time limited, non-sublicensable, non-transferable, royalty free right to use the Licensed Rights and any of its Quality Information for the sole purpose of providing the Services to the Customer and Sol-Gel with respect to the Products during the Term strictly in the manner permitted under this Agreement (the “Manufacturing License”).

  • Following an accreditation event the LHN will provide to the Executive Director, Quality, Information and Performance: • A copy of the ‘not met’ report within two days of receipt by the LHN; • The accreditation report within seven days of receipt by the LHN, providing no significant patient risks have been identified; • Immediate advice should any requirement of a rectification period after the accreditation event not be met resulting in the facility not being accredited.

Related to Quality Information

  • Safety Information means (a) any Adverse Event, including any Adverse Event related to a quality defect or received through a medical information inquiry, or (b) any Adverse Event related to a report of falsified or counterfeit medicinal product or (c) any of the following with or without an associated Adverse Event:

  • Third Party Information means confidential or proprietary information subject to a duty on the Company’s and its affiliates’ part to maintain the confidentiality of such information and to use it only for certain limited purposes.

  • Supplier's Confidential Information means any information, however it is conveyed, that relates to the business, affairs, developments, trade secrets, Know-How, personnel and suppliers of the Supplier, including IPRs, together with information derived from the above, and any other information clearly designated as being confidential (whether or not it is marked as "confidential") or which ought reasonably to be considered to be confidential;

  • Company Information As defined in Section 4(a)(i).

  • Employee Liability Information means the information which a transferor is obliged to notify to a transferee pursuant to Regulation 11(2) of TUPE regarding any person employed by him who is assigned to the organised grouping of resources or employees which is the subject of a relevant transfer and also such employees as fall within Regulation 11(4) of TUPE;