Examples of Regulatory Guidelines in a sentence
The following table illustrates the Corporation's and CBNA's risk-based and leverage capital ratios at December 31, 1997 and 1996: Per Regulatory Guidelines ----------------------------------------------------- Actual Minimum "Well-Capitalized" --------------------- --------------------- ------------------------- Amount Ratio Amount Ratio Amount Ratio ---------- ------- ---------- ------- ---------- ------- December 31, 1997 Tier 1 capital (a): Consolidated..........................
Since December 31, 2011, the business of QLT and of each of the QLT Subsidiaries has been and is currently being conducted in material compliance with all applicable Laws, Orders and Regulatory Guidelines and neither QLT nor any QLT Subsidiary has received any written notice of any alleged material non-compliance or violation of any such Laws, Orders or Regulatory Guidelines.
Since December 31, 2012, the business of Pozen and of each of the Pozen Subsidiaries has been and is currently being conducted in material compliance with all applicable Laws, Orders and Regulatory Guidelines and policies and neither Pozen nor any Pozen Subsidiary has received any written notice of any alleged material non-compliance or violation of any such Laws, Orders or Regulatory Guidelines.
The Specifications and CMC shall be amended or supplemented to comply with Regulatory Guidelines and Requirements and may be amended or supplemented (including, without limitation, for the purpose of incorporating improvements) from time to time by Anthra with the prior written consent of Genchem Pharma, which shall not be unreasonably withheld.
Genchem Pharma agrees that all AD32 supplied hereunder shall be Manufactured in accordance with the applicable Manufacturing Know-how, Regulatory Guidelines and Requirements, and the applicable CMC, and in compliance with all other national, supranational, state and local laws, rules, regulations and requirements applicable in the countries in which the Product containing such AD32 will be Marketed and sold and in effect at the time of the Manufacture thereof.
Specifically, but without limitation, Genchem Pharma shall cause Sicor to maintain all records and samples relating to such AD32 as are reasonably necessary to comply with Regulatory Guidelines and Requirements and other regulatory requirements in such countries in the Territory.
Since December 31, 2013, the business of DPRX and of each of the DPRX Subsidiaries has been and is currently being conducted in material compliance with all applicable Laws, Orders and Regulatory Guidelines and neither DPRX nor any DPRX Subsidiary has received any written notice of any alleged material non-compliance or violation of any such Laws, Orders or Regulatory Guidelines.
Genchem Pharma shall cause Sicor to provide Anthra's Quality Control Department with such quantities of production samples of AD32 manufactured by Sicor and such copies of completed batch records, as are required for the purposes of securing Health Registrations and ensuring compliance with Regulatory Guidelines and Requirements (and only to the extent that Sicor is not permitted to, or fails to, submit such records directly to the relevant Regulatory Authorities on behalf of Anthra).
Genchem Pharma shall cause Sicor to maintain the Sicor Facility in compliance with all applicable laws, rules and regulations relating to the Manufacture of the Validation Batches and AD32, including without limitation the Regulatory Guidelines and Requirements, and with the provisions of this Agreement, at all times during the term hereof.
Since December 31, 2011, the business of Auxilium and of each of the Auxilium Subsidiaries has been and is currently being conducted in material compliance with all applicable Laws, Orders and Regulatory Guidelines and neither Auxilium nor any Auxilium Subsidiary has received any written notice of any alleged material non-compliance or violation of any such Laws, Orders or Regulatory Guidelines.