Procedure Description

Table 2.8. Typical issues addressed when designing a clinical trial protocol. The trial objectives should clearly define what questions the trial should answer. The study design section should contain comprehensive information detailing trial size, criteria used to choose the study population, and enrolment procedures. Description of intervention section should give the background to the intervention itself, its therapeutic rationale and how it is to be administered. Measurement of response should detail the data to be collected, how it will be collected and analysed. The organization and administration section should give full details of all the investigators, where the trial is being run, and its project management details...

Verify the following system recovery procedures Description Status... 

The purpose is to evaluate the bioburden, spore bioburden, and endotoxin present on rubber stoppers and unprocessed glass vials. The similarity of the contents and procedure description shall be considered coincidental due to the similarity of generic methods. 

Measurement of quantities in samples of biological origins Presentation of reference measurement procedures Description of reference materials... 

In these experimental procedures, descriptive terms were collected first. Eight kinds of foods with and without additional MSG or containing different concentrations of broth or stock were served to 180 persons. The subjects expressed freely their impressions of the flavors of the samples using their own terminology. Out of approximately 500 expressions obtained, 32 pairs of the terms frequently expressed were selected except the terms... 

If laboratory tests were used to obtain design data, the experimental data, apparatus and procedure description, and interpretation of the results may be included as a special appendix to the design report. 

S.4.2. Non-linear Parameter Optimization Procedure Description One function at a Time... 

SOP on SOPs This should describe the approach taken to the writing of SOPs within the functional group, the sections, who can authorize the procedure, description of the procedure, and distribution hst. 

Explanation that the study is a research procedure Description of study type and research aims Description of study medications/devices Description of procedures to be followed... 

The method procedure, description, or STM (standard test method) should contain at a minimum the following information prior to validation ... 

PROCEDURES [Description of the operations to be carried out, the precautions to be taken and measures to be applied directly or indirectly related to the manufacture of a medicinal product. 

Procedures are used for a hierarchical description of a design or to break down the description into several smaller parts. A procedural description results in a graph that describes the behavior or semantics of the procedure. The instantiation (call) is done with a node whose type corresponds to the name of... 

Section 8.6 is dedicated to putting into practice the strategy developed in Chap. 7 (for details please return to Sect. 7.8.2.1 on the procedure description and analysis) but now applied to material balance for reactive systems. 

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