The product development lifecycle of drugs is longer than many people think. New therapeutic products, which are drugs or biologics, undergo a complex process that takes approximately 10 to 12 years from start to finish. When you work in clinical research, you will play a role in the industry that brings new drugs and medical devices to market. There are many stages to this process, all of which are important. Without clinical research, this process wouldn’t be complete. Read on to learn more about what’s involved in a drug lifecycle, with a focus on why clinical research is an integral.. READ MORE »
James Lind is thought to be the first person to conduct a clinical research trial. His focus was on scurvy and how it could be treated. Interestingly enough, Lind’s theories and conclusions differ from what we know to be true today. So, although his trials didn’t necessarily lead to the entire answer, they were the beginning of a primary research method used today in the world of medicine. If you’re curious about how a doctor used first-hand experience, previous reports of scurvy, and observations on 12 sick subjects to conduct the first clinical trial, read on! You may learn a.. READ MORE »
When conducting clinical trials, results can depend on how diverse the population of participants is. Clinical trial diversity is essential for: Accuracy Effectiveness Reduction of bias Gender bias in particular is an issue currently being addressed within clinical trials. Because there has historically been a bias towards male study participants in medical research, there is a lack of data by comparison on females and how they react to drugs. Read on to learn why gender diversity in clinical trials is so important, and what can be done to improve it! Why Inclusion Is Important to Graduates of Clinical Research Programs.. READ MORE »
A major benefit of clinical trials is the ability to test on multiple participants, ensuring that an outcome isn’t just tied to one person. However, the diversity of these multiple participants is important, to ensure that the results coincide with how the drug will be used once approved. Sex and race can play a part in how medications work and whether a person is likely to participate in a clinical trial. Read on to learn a little bit more about what you should know about making studies inclusive, accurate, and effective. Why Diversity Matters for Effective Clinical Research Diversity of.. READ MORE »
Novel compounds found in sea sponges have shown promise for pharmaceutical applications. If you’re interested in clinical research training, learn more here.
Clinical trials play a vital role in advancing medical and scientific research. They are a necessary step for developing new drugs or treatments and for better understanding specific illnesses. If you pursue a career in clinical research, you may find yourself helping out in a clinical study in a number of ways, such as by coordinating studies or by serving as a monitor on one. You may also find yourself wondering why people choose to volunteer for clinical studies. The truth is that every person who volunteers for a study is unique and they all have their own reasons for.. READ MORE »
The complexities of the brain are staggering, so grads of clinical research courses are excited about a new link between magnets and memory recovery.
Could the flu virus turn from foe to friend? Here’s what students with clinical research training need to know about its possible utility for fighting cancer.
Height, weight, and gender are some of the standard factors looked at when determining the appropriateness or dosage of a medication, but even accounting for several of these may not result in a perfect solution. Accounting for the very genetic code of the individual who is meant to receive a treatment, though, could be the key to providing the precise care that is best suited for each person. Pharmacogenomics is the study of how the genome affects an individual’s reaction to a drug that enters their system. In an age of heightened focus on genetic modification and engineering, it is.. READ MORE »
New drugs are developed, tested, processed, marketed, and then eventually released to the public every year. During their rigorous testing process, side effects arise in clinical trial patients and are noted by doctors. It is common for drugs to enter the market with a list of side effects, some being beneficial, but most being negative. These negative side effects are known as adverse effects. After a drug has been released to the market, there are systems in place so that healthcare professionals can report any new issues or serious reactions to drug. These are known as adverse drug reactions (ADRs)… READ MORE »