vs. what it actually is vs. what it should be vs. what it could be?
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66. Do you have a Regulatory processes success story or case study ready to tell and share?
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67. What scope do you want your strategy to cover?
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68. Are all requirements met?
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69. Is the scope of Regulatory processes defined?
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70. Is scope creep really all bad news?
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71. What are (control) requirements for Regulatory processes Information?
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72. What critical content must be communicated – who, what, when, where, and how?
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73. How do you manage changes in Regulatory processes requirements?
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74. In what way can you redefine the criteria of choice clients have in your category in your favor?
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75. Are accountability and ownership for Regulatory processes clearly defined?
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76. Is there a critical path to deliver Regulatory processes results?
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77. What gets examined?
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78. Scope of sensitive information?
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79. What is out-of-scope initially?
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80. How do you build the right business case?
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81. Is the current ‘as is’ process being followed? If not, what are the discrepancies?
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82. Has the direction changed at all during the course of Regulatory processes? If so, when did it change and why?
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83. What is the definition of Regulatory processes excellence?
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84. What specifically is the problem? Where does it occur? When does it occur? What is its extent?
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85. What is a worst-case scenario for losses?
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86. What are the Regulatory processes tasks and definitions?
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87. How do you keep key subject matter experts in the loop?
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88. Are improvement team members fully trained on Regulatory processes?
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89. What information do you gather?
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90. What is the scope of Regulatory processes?
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91. What are the boundaries of the scope? What is in bounds and what is not? What is the start point? What is the stop point?
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92. Have all of the relationships been defined properly?
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93. Who defines (or who defined) the rules and roles?
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94. Has a Regulatory processes requirement not been met?
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95. How would you define Regulatory processes leadership?
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96. Is full participation by members in regularly held team meetings guaranteed?
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97. Are team charters developed?
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98. How was the ‘as is’ process map developed, reviewed, verified and validated?
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99. What constraints exist that might impact the team?
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100. Who are the Regulatory processes improvement team members, including Management Leads and Coaches?
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101. What intelligence can you gather?
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102. Have all basic functions of Regulatory processes been defined?
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103. Are different versions of process maps needed to account for the different types of inputs?
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104. Has a high-level ‘as is’ process map been completed, verified and validated?
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105. Do you all define Regulatory processes in the same way?
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106. Is Regulatory processes required?
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107. Are there any constraints known that bear on the ability to perform Regulatory processes work? How is the team addressing them?
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108. Is the Regulatory processes scope manageable?
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109. Have the customer needs been translated into specific, measurable requirements? How?
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110. What system do you use for gathering Regulatory processes information?
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111. What are the compelling stakeholder reasons for embarking on Regulatory processes?
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112. Are resources adequate for the scope?
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113. What is the scope of the Regulatory processes work?
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114. How are consistent Regulatory processes definitions important?
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115. What are the Roles and Responsibilities for each team member and its leadership? Where is this documented?
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116. How do you gather the stories?
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117. Who approved the Regulatory processes scope?
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118. What would be the goal or target for a Regulatory processes’s improvement team?
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119. What is in scope?
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120. What knowledge or experience is required?
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121. Has everyone on the team, including the team leaders, been properly trained?
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122. Is there regularly 100% attendance at