For people in need of medicines, the usual scene is being torn between buying the branded drug written on the recommendation or the generic alternative which is definitely at a lower price. Many people are anxious that given the cheap value of generic drugs, the efficacy and safety may have been risked during the manufacture. However, with the strict regulations currently imposed on medicine creation, all medicines are certified safe and effective before being put on the market. Therefore, there is not need anxious as regards consuming generic medication rather than the branded ones.
People should remember that all drugs go through the examining eyes of the FDA or the Food and Drug Administration. Whether it is a generic medicine or a branded medication, if it did not pass the standards of the FDA, it’ll never be purchased in the market. By this, all medications that can be bought from land-based or internet drugstores are safe and effective in their own right.
Generic drug companies have as much responsibility to the FDA as branded drug institutions. Via the standards of the FDA, whether the medicine is to be sold with a brand name or not, they are still similar medication. Everything is the same in the eyes of the FDA and all medications go through the same level of judgment.
With the intense judgment of the FDA, majority of companies have their own stringent rule for manufacturing. Rather than current drugs which will only unsuccessful based on FDA standards, these companies make sure that there are measures being adhered to during the development of the drug. These measures are adhered to as an assurance that all produce are effective and safe for human consumption.
One measure being followed to make sure that the product is safe is thorough documentation. This is a process wherein all parts of the process are recorded, from the reception of the raw elements, to the end stages of the processing. This is record is then examined by another individual as kind of of double checking. All documents that come out on a process are duly signed as proof. This guarantees that all activities may be tracked and any kind of mistake will easily be seen and addressed.
Another way is the quality control. This indicates that all manufactured medications go through testing at different stages of the process to see if it is of bad quality. This is made to both aspects of the medication. There is the physical aspect examination which involves, examination of thickness, weighing and all. Another aspect is chemical. This points that the drugs are checked for ingredients or components.
While all researched medication go through the said measures, newly designed and thought of medications also have its own test to undergo. If an institution has a new medication in mind, a proposal must be drafted and sent to the FDA for evaluation. All data on the planned medication must be indicated in the proposal. After assessment, the FDA will start investigating the product proposed. A sequence of tests will once again be performed before finally getting an approval.