The pharmaceutical industry is fast-paced and constantly changing and requires a level of innovation and diligence to be successful. If this sounds like you, then you’ll love the Clinical Research, Drug Safety, and Pharmacovigilance program at AAPS. Our program offers students the opportunity to get hands-on experience with administering and monitoring clinical trials and conducting drug safety and pharmacovigilance activities. Many students go on to fill roles as pharmacovigilance officers at large companies, where they directly apply their studies to their new careers. Gaining experience with encounters you’ll likely have on the job, such as the need to learn Pharmacovigilance.. READ MORE »
A number of different procedures require the use of HPLC validation methods, as you’ll discover when you begin courses in pharmaceutical school. Some of these procedures include: Identification tests Testing for impurities (limit tests or quantitative tests) Assay procedures Dissolution tests Particle size determination Each of these tests uses a specific set of validation characteristics to determine if the substance is suitable for the intended use. During the High Performance Liquid Chromatography (HPLC) course at AAPS, you’ll be introduced to this popular method of compound analysis that’s used in various industries such as the pharma, cannabis, biopharma, food, chemical, environmental,.. READ MORE »
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 »
If you’re studying regulatory affairs, you’ve probably already encountered a host of industry-specific terms used to denote different pharmaceutical practices, processes, compliances, measures, devices and more. Within the industry, agreed-upon definitions are developed in order to keep communication aligned and reduce misinterpretations. Upon entering a career in regulatory affairs, maintaining familiarity with common terms will not only help you to avoid confusion but to ensure the safe and lawful operation of the pharmaceutical organization you’re working with. In the field of pharmaceutical development and regulatory affairs, there are some terms that are frequently conflated. While often used interchangeably in the.. READ MORE »
Are you considering a career in the Pharmaceutical Quality Control and Quality Assurance industry? With training in this field, you’ll be qualified to work in pharmaceutical laboratories, utilizing many strategies to ensure that manufactured products and treatments are consistently safe for use. By conducting testing, overseeing manufacturing equipment and utilizing your knowledge of regulatory compliance, you can determine whether pharmaceutical products possess their intended characteristics and identity. While Quality Control (QC) and Quality Assurance (QA) practices have been around for years within pharmaceutical laboratories, technology and other advancements have altered these processes significantly. Not only have labs evolved to improve.. READ MORE »
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 »
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 »
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 »
Regulatory Affairs is an important aspect of the pharmaceutical industry. As a professional in a regulatory affairs role, you’ll play a crucial role in ensuring that pharmaceutical products are manufactured and distributed in compliance with industry regulations. Your work will confirm that pharmaceutical drugs and medical products are safe and effective for human use. The scope of Regulatory Affairs is wide, as it’s essential to ensure compliance at every stage of the development process, including the testing, manufacturing, marketing, and distribution stages. If you’re wondering what a career in Regulatory Affairs could look like, read on to discover a few.. READ MORE »
While pharmacy is the science of the development, preparation, and distribution of drugs, clinical pharmacology focuses on exploring the relationship between drugs and the humans they’re prescribed to. As a subset of biomedical science, clinical pharmacology is underpinned by the application of pharmacological methods and principles to explore how drugs directly affect populations. The discipline of clinical pharmacology connects science with the practice of medicine, ensuring that those receiving drugs are effectively treated and that potential side effects are reduced. If you’re exploring a career in Pharmaceutical Quality Assurance and Quality Control, you’ll be working to ensure that pharmaceutical drugs.. READ MORE »
