logo
logo

Pharmaceutical Courses

4 Tips for Handling Hazardous Materials After Pharma Courses

Hazardous material exposure can lead to adverse effects on anyone, whether an unknowing patient or seasoned healthcare professional. Around 75,000 healthcare workers are occupationally exposed to hazardous drugs, from nursing staff to laboratory research workers, causing adverse health effects. The importance of workplace safety and proper hazardous drug handling is essential for anyone looking to complete training in Pharmaceutical Quality Assurance and Quality Control. Students who pursue careers as laboratory technicians, validation chemists, and more can find themselves in direct need of hazardous material handling training, so continue reading to learn 4 basic tips for these situations. 1. Understand the.. READ MORE »

Taking Pharma Courses? Discover the Basics of Chemistry, Manufacturing and Controls

In order to ensure the safety and consistency of the pharmaceutical products we consume, there must be procedures and standards in place that regulate their quality. If you’re considering a career in Quality Assurance, Pharmaceutical Analysis, or Regulatory Affairs, a significant component of your responsibilities will be ensuring that the processes you’re adhering to align with the defined standards. When it comes to understanding how the practices around the development of pharmaceutical products are maintained, the explanation starts with Chemistry, Manufacturing and Controls, or CMC. CMC is integral to the drug development process itself, defining how manufacturers operate throughout the.. READ MORE »

Studying Regulatory Affairs? Here’s a Look at the Top Biotech Trends in 2021

The biotech industry experiences constant change with progressive knowledge and research emerging in the field every year. Because of these advancements, people are able to receive clearer diagnoses and find more effective treatment options for their conditions.  A certification in regulatory affairs will allow you to enter the biotech industry with knowledge on a wide range of regulations and standards, such as: Regulatory submissions Post-approval activities Regulatory compliance The Canadian Food and Drugs Act Global Regulatory Strategies Students in this program will earn a certification covering 10 different modules to prepare them for a career in regulatory affairs. With extensive.. READ MORE »

Taking Pharma Courses? Discover the Importance of Cleaning Validation

Cleaning procedures are essential for preventing the contamination of manufacturing products. Those procedures must be well-documented, approved, and consistently performed by professionals to ensure the quality and safety of a product. Cleaning validation ensures that the facility and equipment are designed, used, and maintained in a manner that will remove by-products, cleaning agent residues, or microorganisms from new products.  In the pharmaceutical industry, regulators expect to see a validation program with documented evidence that a process will consistently lead to a product that meets quality standards. In other words, the compliance, quality, and safety of drug products depend upon a.. READ MORE »

Studying Regulatory Affairs? The Importance of GMPs for Natural Health Products

The pharmaceutical world is bound by a number of rules and regulations designed to ensure both quality and safety when manufacturing new drugs. Natural health products (NHPs) are no exception. NHPs are defined as vitamins and minerals, herbal remedies, homeopathic medicines, probiotics, and other products like amino acids. Since NHPs don’t require a prescription for sale, they must be safe to use as over-the-counter remedies. This is where good manufacturing practices come into play. From quality and risk management to ongoing post-marketing activity, Good Manufacturing Practices (GMP) compliance is required at multiple stages of NHP production. This blog will explore.. READ MORE »

Studying Regulatory Affairs? Uncover Key Insights on Regulatory Labelling

Regulatory affairs play a key role in ensuring the public’s safety and well-being, affecting the pharmaceutical and health industry in profound ways. Those interested in studying regulatory affairs are able to better understand regulatory systems, legislations, and practices that impact the development and quality of pharmaceutical goods.  Here, students have the opportunity to explore regulatory labelling—which is essential across a wide range of industries, especially in the pharmaceutical world. With this background, students can better understand (and consequently meet) the labelling and product summaries requirements after completing the program. Equipped with this knowledge, students can become professionals who are ready.. READ MORE »

The Role of Pharmacopeias in Pharmaceutical Quality Assurance

Pharmaceutical professionals have extensive knowledge to analyze the raw materials, processes, and finished products to determine the safety and efficacy of a new drug. Pharmaceutical quality assurance is a crucial practice in the manufacturing practice. This is where pharmacopeias come into play.  Pharmacopeias are documents designed to provide public standards relating to the quality, safety, and efficacy of a drug. Today, pharmacopeias play a major role in the regulatory process and control of pharmaceutical ingredients. Analysts for pharmaceutical quality assurance will draw upon these standards in their methods of quality control. With the global expansion of drug manufacturing and standards,.. READ MORE »

Over the Counter vs. Prescription Meds: A Look for Those in Pharmaceutical Training

All kinds of medications are used to help relieve pain, prevent illnesses, manage diseases to avoid further complications, and much more. These medications typically fall into two categories: prescription (Rx) drugs and over-the-counter (OTC) drugs.  There are many important differences between these two broad categories, which are important to regulatory affairs. Continue reading to explore the differences between both categories while gaining a brief look into some of Canada’s regulatory measures regarding Rx and OTC drugs.    A Basic Overview of Over-the-Counter Drugs  As you get ready to take online pharmaceutical courses, what are some important things to know about OTC.. READ MORE »

How to Stay Committed to Your Studies When Taking Online Pharma Courses

With the inter-connectedness of the internet, professionals can now choose to up-skill and re-skill from the comfort of their homes. It’s possible to become educated in complex, interesting pharmaceutical subjects without needing to physically attend a class. This carries many benefits, including:  Saving time on travel to and from school Attending class from a comfortable environment  Constant access to course materials  Flexibility of location  However, online courses may present difficulties in terms of self-direction. Because it is ultimately up to the student whether they study, attend online lectures, and remain focused on the subject, it may be easier for some.. READ MORE »

4 Facts About the Karl Fischer Titration Method for Students in Pharmaceutical Quality Control

Karl Fischer was a German chemist who discovered that the Bunsen Reaction between iodine and sulfur dioxide could be modified to help determine water content in a non-aqueous system. In 1935, he published this new method, which came to be known as Karl Fischer titration.  To learn more, let’s take a look at a few interesting facts about this very important titration method!  1. It Has Several Applications Crossing Many Industries As a student of pharmaceutical quality assurance, you will soon learn about the Karl Fischer Titration method. This method is one of the most accurate procedures for determining the.. READ MORE »