Owing to the advances in molecular biology and bioinformatic screening technology over the past few years, a wide variety of possible intervention strategies can be designed. As regards to the vaccine development, there have been efforts to select a target antigen (a viral protein or protein fragment) which can induce antibody production in the host. The debate regarding the use of the entire spike glycoprotein or only the key sequences remains to be resolved based on success of the vaccine trials. Nucleic acid (DNA or RNA) based platforms have also been posited as viable contenders. These have been shown to be more stable and simpler to manufacture compared to more traditional vaccines as they can be made only using synthetic biology, eliminating need for prolonged culture. Some key challenges are optimizing the design of the antigen to be used, proper animal models, undesirable immune responses in the vaccine recipient and downstream manufacturing issues of production. Vaccine development, being a trial and error process, requires time and effort. At each step, informed decisions need to be taken whether to invest in a particular candidate vaccine. Needless to mention, safety and efficiency are two integral factors to be prioritised throughout the design process. And finally, feasibility of large-scale production dictates the commercialization process.