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 »
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 »
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 »
Quality assurance can be understood as the process-oriented aspect of quality management, where specific procedures and processes are followed to ensure that the final product meets all industry standards. In this way, quality assurance becomes essential, preventing defects and mistakes throughout the manufacturing process. With a background in pharmaceutical quality assurance, professionals can pursue a career as quality assurance technicians. Here, they can complete a variety of tasks to ensure the top quality of pharmaceutical products—checking quality systems and conducting quality assurance audits among many other responsibilities. Through their efforts, the proper processes and procedures can be implemented to create.. READ MORE »
Dissolution testing is a process where pharmaceutical products such as oral drugs are tested for quality control purposes, to help determine how quickly the drug is released, and aid multiple other aspects of its development. Without this form of testing, a drug’s efficacy would be much harder to gauge. Knowing how to test solid oral dosage forms and evaluate their performance is a great skill to learn for anyone pursuing a career in food and pharmaceutical research and development. But how has this process come to be? And how do oral drug products such as capsules and tablets go through.. READ MORE »
What is Quality by Design (QbD)? It’s an approach to pharmaceutical product development, where an objective is defined prior to starting the process and quality is instilled before manufacturing. Risk assessment and management are a priority and are used as the basis for process control. This can help to: Shorten development times Improve manufacturing quality Further assure safety and efficacy of pharmaceutical products While it takes more time at the beginning of a process, it allows for less stop-and-start along the rest of the development journey. Quality is implemented directly into the workflow, taking into account how the product’s characteristics.. READ MORE »
Pharmacokinetics (PK) and pharmacodynamics (PD) are two core concepts of pharmacology and they are especially important for drug safety and pharmacovigilance. These concepts tell researchers a lot about how drugs move in and interact with the human body, which in turn helps scientists, doctors, and pharmacists know how drugs can be used safely by patients. Below we will compare PK and PD and take a look at why they are both so important for creating safe and effective pharmaceuticals. Both PK and PD Are Equally Important for Pharmacovigilance Certificate Students to Know Both PK and PD are considered to be.. READ MORE »
Interested in pharmaceutical quality assurance? Find out how the World Health Organization plays a key role in developing global quality assurance standards.
There is much to look forward to when pursuing a career in pharmaceuticals. You’ll be entering a cutting-edge field always seeking to improve and uncover innovative new treatments. You’ll have the opportunity to challenge yourself and grow professionally. And perhaps most important of all, you’ll have the opportunity to make a lasting and positive difference in the lives of others. What many students and graduates may not look forward to is the job application process, whether navigating interviews or trying to craft the perfect cover letter. Fortunately, caring colleges offer plenty of services to students. At AAPS, students even have.. READ MORE »
Students in pharmaceutical school take note: pill regimens and daily injections could soon be replaced with advanced medical implants that do the dosing for you.
