Even the most authoritative opinions and old habits are not enough to decide whether a certain treatment will benefit a patient and if the benefits outshine the adverse effects. Sound scientific evidence is required to indicate a drug’s potency and safety before it can be rolled out on the market. Integrated Neurology Services is a leading firm in clinical research in Falls Church, which is dedicated to ensuring the development of quality medicines and medical equipment.
Clinical trials are vital in ensuring prudent use of resources by preventing the use of harmful products and abandonment of effective treatment methods. This has made it possible for the sharing of resources in the treatment of different diseases. Below are the reasons why clinical trials are vital.
They Bring New Treatments to the Market
Each product that has undergone clinical practice, including medicines and devices, has gone through rigorous testing prior to being granted permission for use in your doctor’s office. Without clinical trials, there would be no discoveries in the medical field. With new strains of diseases being discovered every day, it is critical for players in the medical field to be proactive to help save lives and end patients’ suffering.
They provide good information
Assume there are five drugs licensed to treat a particular condition. Without clinical trials, your doctor can use the trial and error method when treating patients to see which one will provide a cure. That would not do. Clinical trials enable medics to systematically test and determine which drug is more effective.
They Take Out a Physician’s Bias
Physicians want to do what is best for their patients at all times. However, it is normal for one to become unintentionally biased by thinking that a new drug is more effective than an old one, which is not always true. The only way to establish the truth is by conducting clinical research to provide better clinical care and enable physicians to be systematic in their medical practice.
They Test Safety and Efficacy
Before a new treatment is introduced into the market, it has to be ascertained to be safe and effective. Each product has to pass through four stages and be subjected to different regulatory authorities including FDA, IRB, OHRP, and USDA, among others. Once the treatment method has received the green light into the market, it is subjected to further safety checks.
The Results Can Affect Many More Patients
Involvement in clinical research can impact thousands of lives. Even though taking part in clinical trials may, at times, not avail help to existing medical challenges, the results might prove useful in responding to new strains of diseases in the future.
Testing Begins with Adults
Only a small percentage of drugs and vaccines used on kids are tested on them. This is so because children and adults have varying metabolism and physiological needs. When testing drugs meant for kids, researchers want to ensure that the drug is safe when used on adults. If the results demonstrate that the drug is safe, it can be cascaded to older children and, eventually, younger children.