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Pharmaceutical Courses

Good Document Review Practices to Integrate for Those in Pharma Courses

Documentation has long been an important aspect of quality assurance roles across the pharmaceutical industry. While good documentation practices can be especially helpful during audits, inspections, and investigations, their utility doesn’t stop there. Documentation is a mandatory aspect of production at all levels to ensure that the products and processes of the facility remain up to standards. With quality assurance training from the Academy of Applied Pharmaceutical Sciences, you will have the opportunity to work in a state-of-the-art laboratory that simulates working in a GMP environment. By practicing what you’ll be doing in your career down the line, you can.. READ MORE »

The Role of Statistics in Pharmaceutical Quality Assurance

A fundamental requirement of the pharmaceutical industry is to ensure the safety and effectiveness of products. Pharmaceutical quality assurance is a vital step in this process and helps to keep all steps and processes in line with good manufacturing practices (GMP). When documentation and data are consistently accurate, then pharmaceutical companies are able to operate and perform as expected. Within pharmaceutical quality assurance roles, this tracking of data is where statistics comes into play. Statistical methods are essential to the operations of any pharmaceutical manufacturing facility, ensuring alignment with standards of quality. Especially considering advancements in technology, coupled with new.. READ MORE »

Common Applications of HPLC You’ll See After Pharmaceutical School

HPLC, short for high-performance liquid chromatography, is a method of separating a mixture of compounds. HPLC offers a unique advantage, producing highly accurate identification, quantification, and purification of a certain compound or analyte. This allows professionals to perform analysis and determine specific results from the sample’s components and identify the exact substances within a mixture.  During the HPLC process, in the stationary phase, a mixture in mobile phase moves through a column at a velocity determined by the nature of the particular chemical, the mobile phase composition, and the type of column. The length of time it takes the components.. READ MORE »

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 »