Pharmaceutical Certifications

Studying Drug Regulatory Affairs? Here Are the Pros & Cons of Generic Drugs

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 »

Prophylactic vs. Therapeutic Vaccines Explained for Students in Pharmaceutical Courses

Vaccines are one of the most useful medical creations of all time. They involve introducing antigens—a substance that the immune system will attack, like dead or weakened viruses—into the body, typically via injection. This can allow people to develop immunities to a range of illnesses, and also to do a better job of fighting against illnesses they have. Many illnesses—like measles, mumps, polio, and more—were once incredibly deadly and affected many people. By preventing the spread of deadly diseases and helping people manage illnesses they already have, vaccines have saved millions of lives over the past centuries. Today, there are.. READ MORE »

Pharmaceutical Quality Assurance Pros Rejoice: A New Alzheimer’s Drug May Slow Mental Decline

It is estimated by the Alzheimer Society of Canada that about 564,000 Canadians will suffer from dementia in 2016. Medical professionals will diagnose an additional 25,000 cases every single year, and by 2031 it is believed the number of patients suffering from dementia will rise to 937,000. Dementia is a huge problem not only in Canada, but across the globe. Unfortunately, there haven’t been any significant scientific breakthroughs that could slow the progress of the disease—until now. If you’re a student enrolled in a pharmaceutical program, you may understand the groundbreaking impact this scientific breakthrough could bring to dementia patients… READ MORE »

Adverse Effects VS Adverse Drug Reactions: 3 Differences for Students in Clinical Research Training

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 »

A Day in the Life of a Pharmaceutical Quality Assurance Associate

The pharmaceutical industry is one of the most regulated industries on the planet—and with good reason. Whether a pharmaceutical product is providing much-needed pain-relief to a patient or helping to rid them of a tough bacterial infection, pharmaceutical products need to work properly and predictably each time they are taken. That’s why drug manufacturers need to employ dedicated professionals with a top education in order to ensure that pharmaceutical products are always of the highest quality. If you’re interested in this in-demand career path, then completing your diploma in quality assurance and quality control is crucial. Throughout your training, you’ll.. READ MORE »

Where Does GMP Training Come From? A Brief History of Pharmaceutical Regulation

Today, many of us take for granted that when we use a medication, we are certain that all of the contents inside the package are written out on its label. We know that our pharmaceuticals are safe and that they have been properly manufactured, tested, and labelled by dedicated professionals with GMP training. But what was life like before there were good manufacturing practises? Before strict regulations were in place and trained professionals knew how to properly test products for consistency and safety? Read on to learn what Canada’s pharmaceutical industry was like before regulation, and find out how important.. READ MORE »

Clinical Research, Drug Safety and Pharmacovigilance Certificate Program

Are you interested in a career in any of the following fields? Clinical Research Coordinator Quality Control in Clinical Research Drug Safety and Pharmacovigilance Pharmaceutical Project Management Clinical Data Management Clinical Research Project Leader If yes, AAPS is happy to announce that our Clinical Research, Drug Safety and Pharmacovigilance Certificate Program might be right for you! Courses can be taken in-class and online, and cover topics such as: Adverse Drug Reaction Reporting Clinical Research SOP Development GCP and GVP Inspections & Audits Clinical Study and Safety Reporting Activities Interpersonal Skills and Negotiation Techniques Post Marketing Compliance for Safety Monitoring Global.. READ MORE »

5 Common Interview Questions for Pharmaceutical School Grads

Job interviews are always stressful. And when you’ve just graduated and are looking for your first job in a new career, it can be even more daunting than usual. The stakes can seem higher, and you want to make the best impression possible. For pharmaceutical quality control students, there are added challenges. Companies in the sector tend to conduct extremely detailed interviews, not only discussing your personal experience and goals, but also asking about quality control and quality assurance practices, often in great detail. It can be an intimidating experience for graduates, but with the right knowledge and a little.. READ MORE »

Dissolution Testing: An Important Part of Pharmaceutical Quality Assurance

Ensuring the quality of pharmaceutical products is an important task. After all, if a manufacturing mistake produces a batch that dissolves slower than normal, patients might accidentally take an extra dose, thinking that they need the added medication to receive the care they need. While these mistakes are rare, it’s still essential for pharmaceutical quality assurance professionals to test the rate at which drugs dissolve. How do quality assurance experts measure that rate to ensure batch consistency? With the help of dissolution testing. What is Dissolution Testing? Before we can define dissolution testing, we’ll need to look at a few.. READ MORE »

Taking Pharma Courses? 4 Treatment Facts About Seasonal Cold and Flu

Winter has its good points: glistening white snow, the holidays, and evenings relaxing in front of a warm fire. However, one thing no-one enjoys is the coughing, sneezing, aches and pains that go hand in hand with this time of year. In fact, these symptoms are a clear indication that we are approaching the dreaded flu season! With so many of us affected by these viruses on a year basis, it’s no surprise that millions of dollars worth of research goes into trialling pharmaceutical products to relieve symptoms of colds and flu each year. Many pharmaceutical college graduates go on.. READ MORE »

Archives