Hello, I am looking for someone to write an essay on FDA Regualtion for Herbal Supplements. It needs to be at least 750 words.Large corporates today make claims about their products that have no real

Hello, I am looking for someone to write an essay on FDA Regualtion for Herbal Supplements. It needs to be at least 750 words.

Large corporates today make claims about their products that have no real scientific basis and insist that these are well established facts.

This research paper focuses on the approval process of the FDA, that is now required. The DSHEA requires FDA to provide evidence against a product to prove that it’s unsafe. The DSHEA establishes the dietary supplements as food. This means that there in no limit to their access by the public and no set upper limit as to what amount is safe to consume for a given period. The researcher states that it is imperative that new law be enacted and that will bring sanity to the dietary supplements industry. The research paper also suggests that there is need for scientific evidence backing the claims that are made and the new regulations should prompt the companies to state the ingredients within the products on their safety, purity, quality and consistency.

This research paper describes four stages of Drug Approval that are done by FDA to summare the process of drug development and approval, such as Drug Testing in Lab Animals, Center for Drug Evaluation and Research, Clinical Trials by the sponsor of the drug development and NDA Application to FDA.

At the end of the research paper, approval process is named as extremely rigorous with each stage having a large number of guidelines and regulations to be adhered to. However, it helps protect the public from any adverse events that may arise from use of the drug and also guarantees the consumer of effectiveness of the drug.