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In part one of this multi-part blog series, we went over some of the basic qualities and roles played by RTSM systems in clinical trials. Short for Randomization and Trial Supply Management, RTSM systems are vital for both randomization in trials and various tracking and management areas that clinical researchers benefit from in numerous ways....

Within a variety of clinical studies, particularly those utilizing single-blind or double-blind formats, one area that’s often very important is randomization. Over recent years, most clinical research facilities have adopted detailed systems to help with this area, broadly classified as RTSM systems – short for Randomization and Trial Supply Management. At AGA Clinical Trials, we’re...

Within the medical world, including clinical research trials, the secure and safe storage of patient data is of paramount importance. Many medical organizations are moving toward private cloud storage, which is a cloud infrastructure accessible only by a single company or organization, rather than a public cloud that’s open to all. At AGA Clinical Trials,...

In part one of this two-part blog, we went over some of the numerous benefits of eConsent, a term short for electronic informed consent in clinical research. eConsent, which makes several parts of the consent and data collection process within clinical trials far easier and more convenient, has major plusses for not only research trial...

In recent years, a form of data collection involving participants themselves has become more and more popular within clinical research. Known as bring your own device studies, or BYOD, these clinical trials involve patients submitting their data using their own smartphone, tablet or some other self-owned piece of technology. At AGA Clinical Trials, we’re proud...

If you’re considering participating in a clinical research study for the first time, or if you haven’t participated in several years, you might have some basic questions about the professionals who will be on-hand to administer the study. This is natural and completely understandable, as these medical professionals will closely interact with you and other...

Within any clinical trial, the use of scientific burdens of proof is a very important theme. Through elements like blind- and double-blind studies, placebos, control groups and others, the goal is to arrive at scientifically and statistically significant results that can be proven using real, tangible evidence. At AGA Clinical Trials, all of our medical...

In part one of this two-part blog, we went over some of the reasons why participating in a clinical trial may benefit you. While participating in clinical research is known to bring several positives to the general medical community, some think of it as a thankless individual task – this simply isn’t the case. At...

While most who haven’t participated in them may not know much about clinical trials, one related term that even many outside the medical community are well aware of is the “placebo effect.” Commonly used in many ways, including some that might not actually be correct, the placebo effect refers to the power of the mind...

Questions and Disclaimers Before Clinical Trials If you’re considering participating in a clinical trial in the near future, whether for a condition you have or as a healthy volunteer, you’ll be doing a great service if you choose to move forward. These studies can make a huge difference for care for various conditions into the...