In the year 2000, there were roughly 2,000 clinical trials being conducted in the United States. Fast forward to 2019, and that number had exploded to almost 320,000. In general, as the number of registered clinical trials has increased in recent years, so has trial complexity. This complexity mirrors the overall rise in the cost of drug development, which has more than doubled every decade since the 1970s and now sits at around $2.6 billion. Increased costs, coupled with a higher percentage of trial failures and an increase in patient-centric trials, have caused a surge in demand for technology adoption in clinical trials. In fact, virtual clinical trials are projected to grow from $4.8 billion in 2018 to $7.6 billion in 2022 with a CAGR of 12.4% according to Beroe Inc. Yet despite this growth, for most patients, finding a clinical trial is still a trying process, with enrollment and participation bringing new challenges.
Clinical Research Training studies are always in need of volunteers. Without these volunteers, medications and treatments cannot be approved by the concerned authorities and thus cannot reach the patients. Apart from gaining access to a potential treatment for a particular disease, other perks include receiving care at the topmost facilities, helping science, and making a potential impact on all those living in that particular condition. These studies generally offer generous compensation for your participation.As the best clinical research courses based on clinical trials strive to investigate if a potential treatment is both safe and effective, there is a certain level of risk associated with it. When the recruited volunteers are chosen, there is a possibility that the treatment shall not be effective, and the volunteer can also be subjected to certain side-effects.
The most commonly asked question by the volunteers of any clinical trial recruitment process is the protection given to them. There are a number of measures that are taken to ensure that the participants of the trial are well protected and safe during the trial. The concerned authorities constantly review the protocols of every trial to ensure that it is done ethically and the patients' rights are protected. Apart from this, the FDA provides oversight for clinical trial testing of medical devices or drugs. Prior to human clinical trials, the FDA reviews the applications for the new treatments and medications to ensure that the studies and researches have protections in place for the volunteers. The completely informed consent forms of the patients are one of the most important pieces of the puzzle of any clinical trial that protects the volunteers. Any changes in the mind of the volunteers enable them to withdraw from the trail immediately, ensuring their complete safety.
Clinical research trainings are given to every professional involved in the trial. Clinical research trainings are continuously updated based on the disease and development of technology to ensure the complete safety of the participants of the trial.