We can work on The core, actual, and augmented product benefits.

Today, there is a great multitude and varieties of new products available in stores and online, from which consumers can choose. Think about the new products you’ve seen in the past two or three years, then choose a new product from any category.

  1. How would you define the attributes and benefits of the chosen product?
  2. Define the core, actual, and augmented product benefits.
  3. Briefly describe the steps in the new product development process.
  4. Each product will have a life cycle, although its exact shape and length are not known in advance. Explain each step in the PLC.
  5. What are the dimensions upon which a company manages its product portfolio?

Sample Solution

phthaloyl (o-carboxybenzoyl C8H5O3) gatherings along these lines, HPMCP is a cellulose where a portion of the hydroxyl bunches are supplanted with methyl ethers, 2-hydroxy propyl ethers, or phthalyl esters. Various sorts of hypromellose phthalate are industrially given sub-atomic loads in the range 20 000–200 000. Ordinary normal qualities are 80000–130000 [133]. These sorts are (HP50, HP55 and HP55S) where HP55 grade is generally utilized for enteric covering, HP55S grade, as a result of its higher level of polymerization contrasted and HP-55, it have more noteworthy arrangement thickness, more noteworthy mechanical quality of the film and HP-50 breaks down at a lower pH esteem and is consequently proper for arrangements which are intended to crumble in the upper piece of the small digestive tract. Exchange name Eudragit S100 HPMCP HP-55 Compound name Poly (methacrylic corrosive, methyl methacrylate) 1 : 2 [128] Cellulose, 2-hydroxypropyl methyl ether, phthalic corrosive ester [133] CAS number (25086-15-1 ) [128] ( 9050-31-1 ) [133] pH solvency ≥ 7 [128, 129] ≥ 5.5 [139] The most widely recognized three techniques used to set up the nanoparticles are: (1) scattering of preformed polymers; (2) direct polymerization of monomers utilizing traditional polymerization responses; and (3) ionic gelation or coacervation of hydrophilic polymers. Notwithstanding, different techniques like supercritical liquid innovation [140] and molecule replication in non-wetting formats (PRINT) [141] can be additionally used to get ready nanoparticles. Polymeric nanoparticles (PNPs) can be set up from preformed polymers through a few techniques, for example, dissolvable vanishing, salting-out, dialysis and supercritical liquid innovation which including the quick development of a supercritical arrangement or fast extension of a supercritical arrangement into a fluid dissolvable. Conversely, PNPs can be legitimately integrated through the polymerization of monomers utilizing an assortment of polymerization methods like smaller than expected emulsion, miniaturized scale emulsion, without surfactant emulsion and interfacial polymerization. The decision of readiness strategy is made based on various factors, for example, the kind of polymeric frameworks, the territory of use, size necessity, and the medication to be stacked. Since, strategy for arrangement for the most part influence the properties of created nanoparticles, it is profoundly favorable to have planning procedures close by to get PNPs with the necessary properties for a specific application. The term nanoprecipitation alludes to a very straightforward preparing technique for the fabricati>

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