(Q) Live Social Enterprise Creation Project

In this first step of the Live Social Enterprise Creation Project, students will identify a social enterprise-related problem, fully frame and validate it, and then develop initial ideas for how to solve the problem. The emphasis at this stage is on deeply understanding a specific problem that a particular group of people have; one that can be solved by the creation of a new social enterprise. Students will identify a few initial solution ideas at this stage, but emphasis is on the problem.
ProblemStudents will identify a social or environmental problem that they wish to address, selected from among the 17 UN Sustainable Development Goals (UN SDG). They will fully explore, frame and validate their chosen UN SDG problem, such that they identify a specific unmet need that a specific group of people experience. The validation work will involve considerable interaction with the problem-holders (people who experience the problem that we wish to address).
The final, framed problem will represent the foundation of your future social enterprise.
Solution(s)At this point only initial solution ideas are required. They should show some creative thinking/innovativeness, but they are not expected to be validated or well developed at this point.
PresentationPrepare and deliver a 90-second presentation designed to attract potential partners (and investors) to support your venture. All team members must have a live speaking role in the presentation.
• Focus: Your presentation will focus on the problem your venture will address. Communicate and demonstrate to your audience that your specific, well-framed problem—which a particular group of people experience—is one that is real and important. At the end of your presentation, your audience should feel that they know exactly what the problem is, who has the problem, and that it is worth expending effort to solve this problem.
• Secondary Communication: You will give some examples of innovative solutions to the problem; initial ideas you would like to explore and test, but you will not have much detail or development of these at this stage.

As of late, new APIs have progressively diminished in dissolvability and is assessed that roughly 70% of new substance items have low solvency in both fluid and natural environments.1 This has prompted one of the fundamental defies of the drug business, demonstrating that compelling medication conveyance frameworks are pretty much as fundamental as pharmacodynamics and viability of a medication. The bioavailability of a medication, is the estimation of how much regulated drug arrives at foundational dissemination. The wide assortment of physicochemical variables which influence bioavailability are thusly thought to be in pre-/present detailing on accomplish proficient medication conveyance. In a perfect world, for oral arrangements, high cell penetrability and high dissolvability, successfully accomplishes an ideal high bioavailability. Figure 1.1 FDA endorsed schematic of the Biopharmacetuical Grouping System2 The biopharmaceutical order framework (BCS) was supported by the FDA in light of the past exploration of Amidon et al.3 The framework is a schematic of boundaries restricting bioavailability, where Class 1 has the most noteworthy bioavailability, Class 4 the least. 1.1 General issues with drug conveyance In watery conditions, hydrophilic medications are promptly broken down in spite of the fact that issues with assimilation happen because of the hydrophobic states of cell films. This implies that the cell penetration pace of hydrophilic medications restricts the general bioavailability, because of the reduction in capacity to diffuse across the cell membrane.1 Hydrophobic medications are by and large the inverse, where the disintegration rate and unfortunate solvency thusly diminishes the general bioavailability. For oral definition, the expansion of a polar practical gathering onto the design of a potential Programming interface is a demonstrated method for upgrading the fluid dissolvability of hydrophobic drugs.4>
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