Posts Tagged: Pharmaceutical school

Diploma vs Certificate: Which Pharmaceutical School Path is Right For You?

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 »

A Look at Post-Approval Activities in Pharmaceutical Regulatory Affairs

When a drug is given regulatory approval to enter the marketplace, a much broader patient population than documented in clinical trials is exposed to the product. Not only is there less control on drug prescription than in a clinical trial, but there is also the chance that certain populations taking the drug may not have been closely studied. Sometimes, rare adverse effects are not even discovered until a product is in its post-approval phase.  As a regulatory affairs professional, you will play an important role in ensuring that pharmaceutical companies keep public safety a priority even after a drug is.. READ MORE »

3 Critical Parameters to Examine During HPLC Validation in Pharmaceutical School

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 »

Considering Pharma Courses? A Day in the Life of a Clinical Research Monitor

A clinical research monitor wears many hats throughout their career. They may step in as a coordinator of people and processes, an overseer of clinical research, and an expert in document review. Depending on the day, the roles may look different for a clinical research monitor, which requires these professionals to remain dynamic and flexible in their day-to-day tasks.  At the Academy of Applied Pharmaceutical Sciences, students in our Clinical Research, Drug Safety and Pharmacovigilance Post-Graduate Diploma Program learn the essential skills required to enter the industry. Many graduates go on to play a vital role in protecting the public.. 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 »

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? Here’s What You Can Expect as a Quality Assurance Technician

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 »

The History of Dissolution Testing for Those Interested in Pharmaceutical Training

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 »

3 Facts About Quality by Design for Students in Quality Assurance and Quality Control Courses

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 »