Poorly water-soluble drug candidates are becoming more prevalent. It has been estimated that approximately 60-70% of the drug molecules are insufficiently soluble in aqueous media and/or have very low permeability to allow for their adequate and reproducible absorption from the gastrointestinal tract (GIT) following oral administration. The attempts of various scientists to transform the liquid self-emulsifying drug delivery systems (SEDDS) to solid-SEDDS by adsorption, spray drying, lyophilization, melt granulation, extrusion, and so forth to formulate various dosage forms like self emulsifying capsules, tablets, controlled release pellets, beads, microspheres, nanoparticles, suppositories, implants, and so forth have also been included. Formulation of SEDDS is a potential strategy to deliver new drug molecules with enhanced bioavailability mostly exhibiting poor aqueous solubility. The self-emulsifying system offers various advantages over other drug delivery systems having potential to solve various problems associated with drugs of all the classes of biopharmaceutical classification system (BCS). Poorly soluble drug candidates have become additional important. It’s been calculable that some 60-70% of the drug molecules are insufficiently soluble in binary compound media and/or have terribly low permeableness to permit for his or her adequate and duplicatable absorption from the alimentary canal (GIT) following oral administration. The tries of varied scientists to remodel the liquid self-emulsifying drug delivery systems (SEDDS) to solid-SEDDS by sorption, spray drying, desiccation, soften granulation, extrusion, so forth to formulate varied indefinite quantity forms like self emulsifying capsules, tablets, controlled unharness pellets, beads, microspheres, nanoparticles, suppositories, implants, so forth have additionally been enclosed. Formulation of SEDDS could be a potential strategy to deliver new drug molecules with increased bioavailability largely exhibiting poor binary compound solubility…