AAPS Blog

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A male farmer inspecting cannabis plants in a field after cannabis industry training

Cannabis History: A Guide for Pharma Professionals Transitioning to the Industry

Cannabis has long been a subject of interest in medicine, law, and society. For students in pharmaceutical training, understanding the historical context of cannabis use is essential to appreciating its current medical applications, regulatory challenges, and future potential. From ancient remedies to modern medical use, cannabis’s journey through history highlights its complex role in healthcare and its evolving acceptance in the pharmaceutical field. Ancient Uses of Cannabis Cannabis has been used for medicinal purposes for thousands of years. The earliest recorded use dates back to ancient China, where Emperor Shen Nung is believed to have included cannabis in his pharmacopoeia.. READ MORE »

October 15, 2024

A pharmaceutical professional cleaning instrument containers with a cleaning cloth after pharmaceutical training

New Workshop! Understanding Cleaning Validation in the Pharmaceutical Industry

As the pharmaceutical industry grows, ensuring product safety and quality has never been more crucial. One key component of this process is Cleaning Validation, a practice designed to prevent cross-contamination between pharmaceutical batches. To help professionals excel in this essential area, AAPS is offering a new comprehensive Cleaning Validation Workshop scheduled for October 17, 2024. This workshop will give participants a robust understanding of Cleaning Validation procedures, regulatory compliance, and hands-on experience in a GMP laboratory setting. Let’s explore what this exciting workshop offers and why it’s a must-attend event for professionals in Quality Control (QC) and laboratory operations. What.. READ MORE »

October 8, 2024

An image of AAPS Clinical Research, Drug Safety, and Pharmacology graduate Prajakta Gawde

From Classroom to Industry: AAPS Clinical Research Graduate Prajakta Gawde’s Success Story

At AAPS, student success drives everything we do, especially in clinical research. Prajakta Gawde, a 2022 Clinical Research, Drug Safety, and Pharmacology program graduate, now thrives in her permanent placement thanks to AAPS.  In this interview, she discusses how AAPS expanded her career prospects in Canada and shares advice for those entering the pharmaceutical sciences. From Pharmaceutical Sciences to Clinical Research Training: Prajakta’s Journey Before joining AAPS, Prajakta had already amassed over five years of experience in the pharmaceutical sciences. Upon relocating to Canada, she was eager to find new career prospects. “I was looking for an opportunity to progress.. READ MORE »

October 7, 2024

Male QA professional verifying information about drugs after completing his clinical research training

Top 5 Emerging Trends in Pharmacovigilance for Clinical Research Students

Pharmacovigilance ensures and safeguards the safety of medications, from their development in clinical trials to post-market surveillance. As the field evolves, staying up to date with emerging trends is vital for anyone pursuing a career in clinical research. Understanding these trends can provide a significant advantage for students enrolled in AAPS’s clinical research program as they prepare to enter the workforce. Below, we explore the top five trends in pharmacovigilance shaping the industry’s future and what they mean for clinical research students. 1. Increased Use of Artificial Intelligence (AI) and Machine Learning (ML) and Big Data Integrating AI, ML, and.. READ MORE »

September 24, 2024

An image of graduate Tolulope Adegbite undergoing pharmaceutical training at AAPS

Bridging the Gap Between Education and Industry: How AAPS Prepares Students for Real-World Pharmaceutical Challenges

What do Tolulope Adegbite, Sowmya Ramachandran, and Henry Vu have in common? Quite a bit, as it turns out. Each pursued pharmaceutical training at AAPS, driven by a passion for growth and excellence and an unwavering determination to overcome challenges in pursuit of their personal and professional goals. While each journey is unique, their experiences highlight an important truth: bridging the gap between education and the pharmaceutical industry requires knowledge, hands-on experience, and a strong support system. At AAPS, we offer education and the tools, opportunities, and guidance to turn academic learning into real-world success. Tolulope, Sowmya, and Henry’s stories.. READ MORE »

September 17, 2024

A GMP concept to be explored in quality assurance training

Preparing for GMP Audits: Best Practices and Strategies

Quality Assurance training is crucial for preparing GMP audits and ensuring compliance with stringent regulatory standards in the pharmaceutical industry. These audits, though daunting, can become opportunities to strengthen your processes, systems, and product quality with the proper preparation and strategies. Below, we outline some best practices for preparing for GMP audits and achieving consistent, successful outcomes. Understand Regulatory Requirements With Our Comprehensive Quality Assurance Training The first step in preparing for a GMP audit is understanding the relevant regulatory requirements. Since GMP guidelines and regulations vary by region and market, staying informed about guidelines specific to your product type.. READ MORE »

September 10, 2024

A good automated manufacturing practice concept to be explored in pharmaceutical training

Introduction to Computer System Validation (CSV) in Pharma

Pharmaceutical training in Computer System Validation (CSV) is essential for maintaining compliance with health authorities like Health Canada, the FDA, and the European Union. CSV ensures that computerized systems in healthcare, including pharma and medical devices, are validated for their intended use. This blog introduces CSV’s importance in pharma, the regulatory landscape, and key components. It also highlights a related workshop by AAPS to help professionals gain foundational knowledge. What Is Computer System Validation (CSV)? Pharmaceutical training teaches that Computer System Validation (CSV) ensures a computer system consistently performs as intended, complying with regulatory requirements. This process is vital in.. READ MORE »

September 3, 2024

A regulatory affairs student, Aishwarya, at AAPS

Championing Student Success: Quality Assurance and Regulatory Affairs Graduate Aishwarya Venkatasubramanian

The Canadian Quality Assurance (QA) industry is tough to navigate, requiring more than just technical skills—it takes determination, education, and experience. Aishwarya Venkatasubramanian, a recent graduate of the AAPS Quality Assurance and Regulatory Affairs (QARA) post-graduate diploma program, exemplifies this. In this blog, we explore Aishwarya’s journey from biotechnology to a successful career in Quality Assurance, with comprehensive support from AAPS College. A Passion for Healthcare and Education Aishwarya’s passion for healthcare has driven her journey from completing a master’s in biotechnology in India to navigating new challenges in Canada. Upon arrival, she balanced her personal life and career ambitions,.. READ MORE »

August 27, 2024

An image of cannabis plant leaves backdropped by the Canadian flag, representing cannabis education in Canada

Canada’s Cannabis Market Six Years After Legalization

Canada made history on October 17, 2018, when it became the first G20 country to legalize recreational cannabis. Since then, the Canadian cannabis market has undergone significant changes. Six years later, this market provides a unique case study for students in cannabis industry training, offering insights into regulatory challenges, economic impacts, and consumer trends. Historical Context and Legal Framework In 2018, Canada became the first G7 country to legalize cannabis for adult use fully. This move aimed to eliminate the illegal market, protect public health, and generate tax revenue. The Cannabis Act set the framework for cannabis production, distribution, and.. READ MORE »

August 20, 2024

A male quality assurance professional analyzing a USP document

Navigating the USP: What Quality Assurance Professionals Must Know

The pharmaceutical and biotech industries are well known for maintaining high standards of quality and compliance, and Quality Assurance (QA) professionals are instrumental in ensuring that products meet the rigorous standards set by regulatory bodies. One of the key resources guiding these professionals is the United States Pharmacopeia (USP), a compendium of drug standards that provides guidelines for product quality, purity, strength, and consistency. Understanding and navigating the USP is essential for QA professionals to ensure compliance and maintain product quality. This blog post explores the USP’s importance and what QA professionals must know to follow its guidelines. The Importance.. READ MORE »

August 13, 2024

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