Abstract:
A diagnostic system is disclosed. In one embodiment, the system includes i) an input interface for use by a person to submit user profile data, physical data and psychological data to the system, the physical data representing heart rate, blood pressure, and other biophysical parameters of the person, the psychological data representing quality of life and needs satisfaction and other psychological parameters of the person, ii) an analyzer for processing the physical data and psychological data to generate risk profile data based on criteria data for conditions and iii) an output interface for providing risk profile displays using the risk profile data to present for the person risk levels associated with the conditions.
Abstract:
A method for consolidating a database in a Seibel CRM environment is presented. Bypassing the Business Object Layer (BOL) of the Seibel CRM environment, primary keys in a consolidated table are realigned such that a consolidated child table, created from two distinct databases, is able to point to reference items in a single parent table.
Abstract:
The present invention provides a pharmaceutical composition for transdermal delivery comprising: one or more physiologically active agents; one or more dermal penetration enhancers; a pharmaceutically acceptable carrier comprising a volatile solvent; and a hydrofluorocarbon propellent; wherein the carrier and penetration enhancers combine to provide a single-phase solution of the one or more physiologically active agents.
Abstract:
A pharmaceutical composition for transdermal delivery comprising one or more physiologically active agents; one or more dermal penetration enhancers; and a volatile pharmaceutically acceptable carrier comprising a volatile solvent; and wherein the physiologically active agent and dermal penetration enhancer form an amorphous deposit upon evaporation of the volatile carrier, said amorphous deposit forming a reservoir within the stratum corneum; and (A) wherein the composition has a release rate profile of physiologically active agent so as to provide a ratio of the maximum concentration (Cmax) to the average concentration (Cavg) for the physiologically active agent over the dosage interval within the range of 1 to 10.