Analytical chemists are skilled and hardworking professionals who utilize advanced instrumentation and techniques to analyze the properties of various substances, including environmental, water quality, and pharmaceutical drugs. Their primary objective is to identify the elemental composition of a substance and gain insights into its structure and interactions. Among the list of available techniques, High-Performance Liquid Chromatography (HPLC) stands out as one of the most widely used methods. This blog post will explore four significant advantages of earning an HPLC certificate for those aspiring to build a successful career as an analytical chemist. 1. HPLC Certificate Qualification Expands Career Opportunities Obtaining.. READ MORE »
The State of Pharma Conference is a virtual pharmaceutical conference that brings together professionals from all areas of the pharmaceutical industry. The conference, which takes place on May 11, is designed to provide attendees with the latest insights, trends, and best practices in the field, as well as opportunities to connect with peers and industry leaders. The pharmaceutical industry is one of the most important sectors for global health, and it is constantly evolving. With so much hinging on their knowledge and performance, professionals in this industry need to maintain sharp, cutting-edge skills to keep up with the ever-changing realities.. READ MORE »
When it comes to pursuing a career in the pharmaceutical industry, there are two main paths to consider: a diploma program vs a certificate program. Both diploma and certificate programs in the pharmaceutical field offer unique benefits, and both can equally lead to rewarding careers in the industry. It’s important to consider your own goals, needs, and the investment of time and money when making your decision. Whether you pursue a diploma or certificate program at AAPS, you will gain valuable knowledge and skills that can help you succeed in the rapidly growing and exciting field of pharmaceuticals. If you’re.. READ MORE »
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 »
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 »
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 »
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 »
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 »
