Continued growth in technology and the upsurge in COVID-19 are some of the factors that have bolstered the popularity of virtual clinical trials today. By reducing site visits and clinics for the tests, most patients find virtual trials an effective way to participate in medical research. On top of this, the use of televisits to collect patients’ data offers a reliable avenue for data screening. Ultimately, through Veristat virtual trials, sponsors can effectively test their oncology trial design to ensure smooth trial processes. As such, virtual clinical trials are advantageous to both the sponsors and the subjects, thanks to the convenience and the efficiency they offer. But you might wonder how exactly virtual clinical trials improve your drug research trials. Below is a look at some reasons why you should consider virtual trials for an effective drug investigation process.
Saves Time and Money
Having your clinical trials conducted onsite requires a huge financial and time commitment. This is burdensome for your oncology clinical trial design considering the situation of cancer patients. Also, stakeholders including clinical staff, researchers, sponsors, and CRO would need significant remuneration in the course of the study. Sometimes, the financial burden is so heavy that the clinical trial has to be halted. To solve this problem, researchers should choose virtual clinical trials over onsite trials. The former only requires investment in data collection tools and network coverage to take place. As a result, they help you save on time and money which you can use to sponsor future clinical trials or better still streamline the current study. Additionally, team members can access the accumulated data remotely hence saving the time they would use to manually access this information.
Offers Patients lots of Conveniences
By not requiring patients to attend multiple site visits, virtual clinical trials offer patients lots of conveniences. Usually, patients attend televisits where their progress is monitored with the help of technology. As a result, most patients find it less burdensome to participate in virtual clinical trials. Barriers such as distance or transport costs are solved by this technological move.
Streamlines Data Collection Processes
In conventional clinical trials, patient records are prone to numerous human errors. As a result, the clinical trial might not produce reliable results which are not biased. With virtual clinical trials, data collection procedures are conducted remotely giving zero to minimal room for errors. As a result, sponsors and researchers have access to accurate data which is necessary for drug testing processes.
Makes Data Screening Fast And Effective
Traditional clinical trials take a lot of time to do the drug testing and screen the data results. As a result, decisions to stop a wrong drug would delay leading to adverse results on the patients in question. It’s, therefore, necessary to take advantage of virtual trials as they fasten the overall process. Usually, when clinical research is conducted remotely, trial investigators can spot inefficiencies early enough and make the necessary changes. Additionally, an ineffective drug can be done away with before more resources are invested in testing it. It would also be possible to make changes to the study plan according to the data accumulated in the initial phases of the trial.
In addition to speeding up the clinical trial process, the virtual trial comes with many other benefits. What’s more, researchers can collect accurate data, which helps them get positive outcomes and complete the research trials successfully.
