Integral approach Sample Clauses

Integral approach. I will follow ▇▇▇▇▇▇▇▇▇▇’▇ proposal for an integral approach to explore ▇▇▇▇▇’▇ thoughts. ▇▇▇▇▇▇▇▇▇▇ already criticised approaching ▇▇▇▇▇ by quoting passages from his treatises almost at random to illustrate a point someone wishes to make. Instead of using Philo as quarry, ▇▇▇▇▇▇▇▇▇▇ emphasised that it is important to have a grasp of the place a certain passage has within a treatise, and what place that treatise has in the whole of ▇▇▇▇▇’▇ oeuvre, to understand what ▇▇▇▇▇ writes about.160 ▇▇▇▇▇▇▇▇▇▇ further presented ▇▇▇▇▇ as 160 Goodenough, Introduction, p. 20. This approach is comparable to what ▇▇▇▇▇ describes as ‘the contextual approach’ in Runia, ‘Naming and Knowing’, pp. 69–72. Runia distinguishes roughly three approaches towards the description of Philo’s theology. These are: first, the systematic approach, where scholars ‘attempt to put together, on ▇▇▇▇▇’▇ behalf, the systematic presentation of his doctrine of God, which he never managed (or dared) to publish’; second, the historical approach, where ▇▇▇▇▇’▇ theology is mainly described and explained by linking and comparing his ideas and concepts to those of other authors, such as ▇▇▇▇▇▇▇▇▇▇ and ▇▇▇▇▇▇▇▇; and third, the contextual approach, where ▇▇▇▇▇ is considered first and foremost an exegete, and where the starting point is taken with the analysis of someone fully integrated and interacting with his cultural surroundings, both on an intellectual and on a more popular level. ▇▇▇▇▇▇▇▇▇▇ did not consider ▇▇▇▇▇’▇ Jewishness as something separated from this cultural background.161 ▇▇▇▇▇▇▇▇▇▇ therefore avoided classifying ▇▇▇▇▇’▇ ideas as either belonging to his Jewish or his Hellenistic background and education. It took quite some time for these views to take hold in Philonic research.162 Although picking through ▇▇▇▇▇’▇ works to illustrate a certain point still occurs occasionally, strictly differentiating between Greek or Jewish elements in ▇▇▇▇▇’▇ thinking is hardly done anymore.163 However, one could consider attributing a special character to ▇▇▇▇▇’▇ interaction with the Bible, setting him apart from contemporary intellectuals who explored other authoritative ancient sources, a rudimentary trace of this approach. Still, the current state of affairs in Philonic research in general is that ▇▇▇▇▇ is considered a Jewish thinker fully engaged and interacting with his intellectual, cultural and political environment, and that it is necessary to consider the full context of a passage to interpret wha...

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  • Contractor Approach The Contractor shall develop, document, and implement BIDM Data Exchanges to obtain BIDM Imports from and to send BIDM Exports to CDPHE's CEDRS. 17.47.2.1. This exchange shall occur on a period as determined by the Department

  • Approach All investments are to be made using the value approach by investing in companies at prices below their underlying long term values to protect capital from loss and earn income over time and provide operating income as needed. With regard to equities, no attempt is made to forecast the economy or the stock market. The manager will attempt to identify financially sound companies with good potential profitability which are selling at large discounts to their intrinsic value. Appropriate measures of low prices may consist of some or all of the following characteristics: low price earnings ratios, high dividend yields, significant discounts to book value, and free cash flow. Downside protection is obtained by seeking a margin of safety in terms of a sound financial position and a low price in relation to intrinsic value. Appropriate measures of financial integrity which are regularly monitored, include debt/equity ratios, financial leverage, asset turnover, profit margin, return on equity, and interest coverage. As a result of this bargain hunting approach, it is anticipated that purchases will be made when economic and issue-specific conditions are less than ideal and sentiment is uncertain or negative. Conversely, it is expected that gains will be realized when issue-specific factors are positive and sentiment is buoyant. The investment time horizon is one business cycle (approximately 3-5 years). As regards bonds, the approach is similar. No attempt is made to forecast the economy or interest rates. The manager will attempt to purchase attractively priced bonds offering yields better than Treasury bonds with maturities of 10 years or less that are of sound quality i.e. whose obligations are expected to be fully met as they come due. We do not regard rating services as being an unimpeachable source for assessing credit quality any more than we would regard a broker's recommendation on a stock as being necessarily correct. In any form of investment research and evaluation, there is no substitute for the reasoned judgement of the investment committee and its managers.

  • Product Changes Vocera shall have the right, in its absolute discretion, without liability to End User, to update to provide new functionality or otherwise change the design of any Product or to discontinue the manufacture or sale of any Product. Vocera shall notify End User at least 90 days prior to the delivery of any Product which incorporates a change that adversely affects form, fit or function (“Material Change”). Vocera shall also notify End User at least 90 days prior to the discontinuance of manufacture of any Product. Notification will be made as soon as reasonably practical for changes associated with regulatory or health and safety issues.

  • Clinical Studies The animal and other preclinical studies and clinical trials conducted by the Company or on behalf of the Company were, and, if still pending are, to the Company’s knowledge, being conducted in all material respects in compliance with all Applicable Laws and in accordance with experimental protocols, procedures and controls generally used by qualified experts in the preclinical study and clinical trials of new drugs and biologics as applied to comparable products to those being developed by the Company; the descriptions of the results of such preclinical studies and clinical trials contained in the Registration Statement and the Prospectus are accurate and complete in all material respects, and, except as set forth in the Registration Statement and the Prospectus, the Company has no knowledge of any other clinical trials or preclinical studies, the results of which reasonably call into question the clinical trial or preclinical study results described or referred to in the Registration Statement and the Prospectus when viewed in the context in which such results are described; and the Company has not received any written notices or correspondence from the FDA, the EMA, or any other domestic or foreign governmental agency requiring the termination, suspension or modification of any preclinical studies or clinical trials conducted by or on behalf of the Company that are described in the Registration Statement and the Prospectus or the results of which are referred to in the Registration Statement and the Prospectus.

  • Clinical Trials The studies, tests and preclinical and clinical trials conducted by or on behalf of, or sponsored by, the Company, or in which the Company has participated, that are described in the Registration Statement or the Prospectus, or the results of which are referred to in the Registration Statement or the Prospectus, were and, if still pending, are being conducted in all material respects in accordance with protocols, procedures and controls pursuant to, where applicable, accepted professional and scientific standards for products or product candidates comparable to those being developed by the Company and all applicable statutes, rules and regulations of the FDA, the EMA, Health Canada and other comparable regulatory agencies outside of the U.S. to which they are subject, including, without limitation, 21 C.F.R. Parts 50, 54, 56, 58, 312, and 812; the descriptions of the results of such studies, tests and trials contained in the Registration Statement or the Prospectus do not contain any misstatement of a material fact or omit a material fact necessary to make such statements not misleading; the Company has no knowledge of any studies, tests or trials not described in the Registration Statement or the Prospectus the results of which reasonably call into question in any material respect the results of the studies, tests and trials described in the Registration Statement or Prospectus; and the Company has not received any notices or other correspondence from the FDA, EMA, Health Canada or any other foreign, state or local governmental body exercising comparable authority or any Institutional Review Board or comparable authority requiring or threatening the termination, suspension or material modification of any studies, tests or preclinical or clinical trials conducted by or on behalf of, or sponsored by, the Company or in which the Company has participated, and, to the Company’s knowledge, there are no reasonable grounds for the same. Except as disclosed in the Registration Statement and the Prospectus, there has not been any violation of law or regulation by the Company in its respective product development efforts, submissions or reports to any regulatory authority that could reasonably be expected to require investigation, corrective action or enforcement action.