Pharmacovigilance ensures and safeguards the safety of medications, from their development in clinical trials to post-market surveillance. As the field evolves, staying up to date with emerging trends is vital for anyone pursuing a career in clinical research. Understanding these trends can provide a significant advantage for students enrolled in AAPS’s clinical research program as they prepare to enter the workforce. Below, we explore the top five trends in pharmacovigilance shaping the industry’s future and what they mean for clinical research students. 1. Increased Use of Artificial Intelligence (AI) and Machine Learning (ML) and Big Data Integrating AI, ML, and.. READ MORE »
It may come as no surprise that COVID-19 significantly accelerated digitalization in clinical research and the pharmaceutical industry. However, new technology introduces new concerns that impact the development of future clinical research. That is also the case with Blockchain technology, introducing many benefits and notable considerations to the field. Students taking a clinical research program know that trust is a key factor in clinical research, and it is drastically changing in the public eye. In today’s society, trust is no longer given by default but is earned through proof instead. As such, “trusted data” becomes a requirement. Blockchain technology could.. READ MORE »
If you are interested in becoming a clinical research professional, your role in the safety and marketing of pharmaceuticals or other product life cycles will be major. Whether you work in pharmacovigilance, with natural health products, cosmetics, or other related industries, understanding the phases of a product’s life cycle is key. As defined by Health Canada, the life cycle of a product includes several stages: Pre-clinical studies Clinical trials Submission of product information to regulatory agency Regulatory agency decision on whether to authorize sale of the product Public access to product Post-market surveillance, inspection, and investigation To learn more about.. READ MORE »
If you would like to combine your interest in science and health,then a career in clinical research may be the right choice. When you study clinical research, you have the chance to learn about topics such as pharmacovigilance practices.These generally refer to how pharmaceutical products are developed, tested, and monitored to ensure they are safe and consistent. One of the key components of pharmacovigilance practices for clinical research,as well as aftermarket surveillance, is safety signal interpretation. Keep reading to learn more about this process and how it factors into clinical research. What Are Safety Signals? As you take courses to.. 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 »
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 »
The complexities of the brain are staggering, so grads of clinical research courses are excited about a new link between magnets and memory recovery.
Developing trials for orphan drugs after clinical research training can be a bit challenging. Find out why addressing the rarest of diseases may get tricky.
Research projects can be complicated to manage. With such high stakes, it’s important that clinical research professionals have top-notch project management skills to keep everything running smoothly. From planning, to determining study goals, budgets, and more, project management has many different aspects that professionals need to keep in mind. Because of these demands, students earning their clinical research diploma become well-versed in the principles of project management during their studies. If you’re considering enrolling in a clinical research program, get a head start on your learning by reading on about how top clinical research professionals manage projects! Pros with Clinical.. READ MORE »
Do you want to start a promising career that allows you to help Canadians across the country stay safe and healthy? If you become a clinical trial and pharmacovigilance professional, you can do just that. Professionals in this field are responsible for the safety of drugs and medical devices. They also make sure that clinical trials are conducted safely and adhere to proper protocol. By ensuring that clinical trials run smoothly, pharmacovigilance professionals help expedite the process of getting life-changing pharmaceuticals to market. These pharmaceuticals can make a huge difference in the lives of people suffering from disease, illness, or.. READ MORE »
