Many individuals associate name brands with quality, and will only substitute brands with cheaper generic equivalents if they can be convinced that doing so is not a downgrade. When it comes to medicine, the dilemma of whether to choose a generic or name brand can be especially difficult. Generic drugs are typically less expensive than the name brands that they replace. However, medicine is not something that many people want to experiment with. If a generic drug doesn’t work as well, the difference could have serious repercussions on a person’s health. Are you considering regulatory affairs training? Read on to.. READ MORE »
In hospitals and doctors’ offices, drugs aren’t the only things responsible for helping patients heal and feel better. Medical devices are a huge category of medical care tools that often go unnoticed, but are crucial to modern day medicine. Medical devices include wheelchairs, medical scissors, and even bandages. They can range from low-tech to high-tech devices and can even include pacemakers. Some of the technologies used to produce them include microelectronics, biotechnology, and even software. Unlike drugs, which dissolve and are absorbed by the body, medical devices are instruments, tools, and implants that can help with everything from diagnosing a.. READ MORE »
Regulatory affairs is a relatively new and demanding career. It requires extensive knowledge of the business, legal, and pharmaceutical aspects of products in development, so that projects can be operated smoothly from inception to market. A regulatory affairs specialist is responsible for keeping up-to-date with all of the rules and regulations that govern the production process for new drugs, cosmetics, and other medical products. And while it is an incredibly rewarding career both emotionally and financially, there are some specific skills that can help you succeed in this profession. If you’re interested in a career that encompasses the specifics of.. READ MORE »
Today’s pharmaceutical industry is very much a global market. While traditional economic powers like the United States remain leaders in the field, new drug development, manufacturing, and trade is now taking place in increasingly diverse parts of the world. In fact, the emerging markets China and Brazil are now home to the 3rd and 6th largest pharmaceutical industries in the world. Not only that, but companies are now manufacturing and developing drugs for distribution to a variety of different countries, each with their own regulations and guidelines. As a result, professionals in the regulatory affairs industry now face a tougher.. READ MORE »
Drug research is essential to helping medicine advance and finding new ways of fighting illness, but it is a long and complicated process. Just one in every 5,000 compounds that enters preclinical testing actually make it to the marketplace, and companies spend approximately US$500 million per product, with studies taking anywhere from 8 to 15 years. For regulatory affairs professionals involved in new drug development, the barriers to making potentially beneficial products available to the public can sometimes be frustrating. Nevertheless, the regulations are necessary to ensure that drugs are safe and effective. So how does a new drug get.. READ MORE »
A career in Regulatory affairs involves doing research and other work that directly impacts the lives of others. If you choose to pursue this career path, you’ll be involved in the research and development of pharmaceuticals, natural products, cosmetics and supplements. On any given day, you’ll be in charge of compiling safety information about a product, negotiating with authorities who control licencing, overseeing clinical trials, and much more. If you are planning to pursue regulatory affairs courses, or have already begun your program, read on to find out what steps you can take to prepare for a job interview once.. READ MORE »
