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Objective organizational

Planning. Through planning, technology managers estabUsh objectives, develop the rationale for these objectives, and estimate the resources required over time to succeed at the strategic business, R D organizational, and project levels. [Pg.131]

The supplementary requirement in clause 4.1.1.1 for goals to deploy the quality policy creates an ambiguity because it is unclear as to whether these goals are the same organizational goals referred to in clause 4.1.1 or some other goals. For clarity, goals are addressed separately under Quality objectives in this chapter. [Pg.98]

Establish whether there is conflict between the stated quality policy, the quality objectives, and the organizational goals and expectations and needs of your customers. [Pg.138]

Many factors influence how a policy is implemented and whether it achieves its objectives effectively. Experience in policy implementation in many areas indicate the importance of good organization. A number of organizational attributes, such as a sound structure, efficient procedures, well-trained personnel and adequate financial resources, are considered cmcial for effective policy execution (18, 19, 20, 21). [Pg.38]

Stage 3 Mild cognitive decline Friends, family, and coworkers begin to notice deficiencies problems with names or words become evident performance issues become evident retention of reading material declines losing valuable objects decline in planning and organizational abilities. [Pg.517]

TABLE 21.5 Defining the problem Describe and define the chemical or physical system(s) from which information must be obtained in order to meet technical or organizational objectives ... [Pg.812]

The first edition1 of this book was published approximately 13 years ago. Its primary objective was to present an overview and a "roadmap" of the process of new drug discovery and development, particularly oriented to individuals or companies entering the pharmaceutical field. It was written by one of the authors (Smith), with no contributors, and drawn on Smith s experiences in the industry and field over the course of nearly 40 years. In the second edition, the scope of the first book has been expanded and technical details in the form of hard data have been included. In addition to the editors own commentary and contributions, the major part of the book is the result of contributions of experts in the industry. New chapters on risk assessment, international harmonization of drug development and regulation, dietary supplements, patent law, and entrepreneurial startup of a new pharmaceutical company have been added. Some of the important, basic operational aspects of drug discovery and development (e.g., organizational matters, staff requirements, pilot plant operations, etc.) are not repeated in this book but can be found in the first edition. [Pg.8]

When the objective is not solely maxitnizing the information from samples but when economic or organizational aspects are at stake as well, there are more ways to influence sampling schemes. Next to the influences of sampling rate as already described there are possibilities in collecting samples in batches and assigning priorities to samples. The influence on laboratory performance and information content has been treated by Vandeginste and Janse 58.59.6o>... [Pg.61]

The implication of this for a manager pursuing a project is that it may not be sufficient simply to get others to assent to your objectives and plans. You have either to make those whose support you need see that what you want is congruent with organizational objectives that they concur with. If these purposes are not already agreed, then you may be faced with the need, unless you choose to act surreptitiously, to embark on the political task of getting organizational purposes modified in a way that incorporates your particular purposes. [Pg.168]

Establishing an organizational structure with identified responsibilities and authorities that allows quality objectives to be met... [Pg.205]


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See also in sourсe #XX -- [ Pg.813 ]




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