Bioengineering is again a new addition to the vast array of thoughts and knowledge of science. Bioengineering as the name itself suggests, is basically using the products of everyday life to create edible vaccines and other kinds of medicines which will not generally have any other side reactions. For example: one day maybe when our kids are sick, we might go to the doctor to get medicine and might return with a granola bar with all the needed medicine in it, all because of bioengineering. There have been several critics about bioengineered edible vaccines which are used. Some say that these medicines have a side effect and cause problem for the patient, like allergies. Several tests have been conducted to verify this allegation. After several tests and uses of the edible vaccines made by bio engineering it has been proved that there are really no risks or side effects of these medicines.
Not only does having an invention like bioengineering save people from the agony of having to take pills but it also helps to protect the safety and prevents any other diseases that can occur from the use of syringes. The pre- filled syringes come with advantages in it. The design of the syringes makes it user friendly and safe for use. It prevents the change of needles, the fear of the same needle being used twice and it also helps in delivering the right medicine and the right amount without the patient feeling cheated about the measurement and the price. The quality that comes with the design makes it something that would have a rapid growth in the pharmaceutical and medical industry in the near future.
If the alternative method of drug delivery is used then it has a great potential to increase the market share because of it being cost effective and hence help in the economic growth of any nation. There needs to certain precautions that need to be kept in mind though about stability and minimal product- packaging interactions.
Some of the main things that will be covered in the conference regarding the pre- filled syringes are to identify the suitable methods to enhance the take up of the product, applying the QbD technique in formulation and packaging. It will also include some tips on implementing successful filling lines and how to ensure total integration of syringe system. Not only will the conference focus on the syringe and it uses but it will also help to give useful tips to the manufacturers about the challenges and solutions to gaining first time regulatory approval and taking steps and approaches to achieving full system validation. It will also help in teaching people about how to employ practices that will minimize the interaction between the drug and the packaging which in turn will become cost effective.

At this conference there will be round table discussions, panels and presentations. There will be several case studies which will be considered and seen during this time. Some of the things that will be covered can be categorized under several sub categories. Some of the points discussed in the tentative agenda are: