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Pharmaceutical Training

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 »

Preclinical Vs. Nonclinical Studies: A Guide for Regulatory Affairs Students

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 »

How the Evolution of Labs Is Shaping Pharmaceutical Quality Assurance

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 »

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 »

3 Careers You Can Pursue After Completing Your Regulatory Affairs Courses

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 »

Clinical Pharmacology Explained for Pharmaceutical Certification Students

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 »

Is Automation the Future of Pharmacovigilance? An In-Depth Look for Students in Pharmaceutical Training

Pharmacovigilance (or PV) is a major part of drug safety, dealing with the detection, assessment, and monitoring of drug effects on the human body. With updated regulations and technological advancements, the pharmaceutical industry is facing pressure to automate PV systems—optimizing spending costs while also improving risk management.  By doing so, PV systems would be better suited to create personalized medicine. Automation would also help promote transparent data sharing between patients and healthcare providers as well as regulatory agencies. In this way, those pursuing pharmaceutical studies can expect automation to significantly change the pharmaceutical industry.  Here’s a closer look at how.. READ MORE »

How Big Data Is Changing the Pharmaceutical Industry: Details for Those Taking Pharma Courses

Big data is a term increasingly used by professionals in the pharmaceutical industry in recent years, as it is considered to be key to furthering pharmaceutical research and development (R&D). When used effectively, the information provided helps facilitate the discovery of a new drug product. The discovery of drugs becomes an easier process, as the data is used to predict how the drug will interact with the person consuming it. This data is also used to make research more efficient and to enhance clinical trials, as well as to facilitate technological innovation and improve client safety. With the use of.. READ MORE »