AAPS Blog

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A team of pharma QA professionals in a laboratory setting

Mastering CAPA: Strategies to Drive Quality and Compliance in Your Organization

In the pharmaceutical and biotechnology industries, Corrective and Preventive Actions (CAPA) are fundamental to maintaining compliance with regulatory standards and ensuring product quality. For professionals in pharma QA or those pursuing quality assurance training, understanding CAPA processes is vital to resolving issues, preventing recurrence, and driving continuous improvement. AAPS’s upcoming webinar, Developing an Effective CAPA Strategy, will dive deep into effective CAPA practices, equipping participants with actionable insights to enhance organizational quality and compliance. Understanding CAPA and Its Importance CAPA is the backbone of a robust Quality Management System (QMS). It provides a structured approach to identifying root causes, addressing.. READ MORE »

January 7, 2025

A male clinical project manager reviewing a project charter after completing his clinical research training

Career Guide: What Is a Project Charter in Clinical Research?

Are you working your way toward a career in clinical research? If so, one document you’ll encounter early and often is the project charter. This tool isn’t just paperwork; it effectively sets the stage for clinical research success. Understanding project charters is essential whether you’re new to the field or sharpening your expertise. Here’s a comprehensive introduction to a project charter and its importance in clinical research. What Is a Project Charter in Clinical Research? In clinical research, a project charter is a high-level document that formally authorizes a project and sets its framework. It’s typically created during the initiation.. READ MORE »

January 3, 2025

An image of the HACCP food safety and quality control concept

Food Safety: Examining Legislation at the Municipal, Provincial, and Federal Levels

Food safety initiatives ensure our food is safe, nutritious, and free from harmful contaminants. In Canada, food safety legislation is enforced at multiple levels—municipal, provincial, and federal—each with its scope and responsibilities. Understanding these legislative frameworks is essential if you’re pursuing a career in food safety or considering food safety training. This blog explores the role of food safety legislation across these levels, with a special focus on the federal responsibilities led by the Canadian Food Inspection Agency (CFIA). Federal Oversight: The Role of the CFIA At the federal level, the Canadian Food Inspection Agency (CFIA) plays a central role.. READ MORE »

December 24, 2024

A focused female pharmaceutical professional taking pharma courses online

7 Reasons to Start Taking Pharma Courses Online in 2025

Are you considering advancing your pharmaceutical career but need help fitting education into your busy schedule? At AAPS, our pharma courses online are specifically designed to help you grow and succeed in today’s competitive pharmaceutical industry.  Here’s why 2025 is the perfect year to plunge into online pharmaceutical education. 1. Flexible Learning That Works for You One of the most significant advantages of online courses is their flexibility. With AAPS, you can learn when and where it’s most convenient for you—early in the morning, during a lunch break, or late at night. Our programs include synchronous and asynchronous learning options,.. READ MORE »

December 17, 2024

A portrait of Parnian Dokouhaki in pharma QA training

Supporting Graduates: In Discussion With Pharma QA Graduate Parnian Dokouhaki

The journey from dream to reality for students eager to enter the Canadian pharmaceutical industry can often feel daunting. The road is challenging between adjusting to a new country and building a career in a competitive Pharma QA market. But with the right guidance, it’s also incredibly rewarding. At the Academy of Applied Pharmaceutical Sciences (AAPS), we don’t just prepare students for the industry; we empower them to succeed. Meet Parnian Dokouhaki, a Pharmaceutical QAQC Program graduate who now works in the Quality Assurance (QA) department at Eurofins. Her journey from student to professional is a powerful example of what’s.. READ MORE »

December 10, 2024

A male professional giving the thumbs-up sign to a CBD oils jar after completing his cannabis courses

3 Reasons a Cannabis Diploma Will Enrich Your Career

The cannabis industry is one of the fastest-growing sectors globally, creating an unprecedented demand for skilled professionals. Whether you dream of working in cannabis production facilities, testing laboratories, retail stores, or beyond, the Cannabis – Management, Quality, and Edibles Diploma at AAPS is your gateway to success. This program equips learners with the academic knowledge, practical skills, and industry insights needed to thrive in entry-level and mid-level roles in this burgeoning field. Here’s how this diploma can transform your career. 1. Comprehensive Program Designed for Industry Success The Cannabis – Management, Quality, and Edibles Diploma delivers a robust curriculum that.. READ MORE »

December 3, 2024

The regulatory affairs webinar image details

4 Highlights From Our Recent Drug Product Submission (NDS) Preparation in eCTD Webinar

Regulatory submissions are a cornerstone of the pharmaceutical industry, and mastering this process is essential for regulatory affairs professionals. On November 8, 2024, AAPS hosted an insightful webinar on Drug Product Submission (NDS) Preparation in eCTD format. The webinar aims to equip participants with practical knowledge and skills for successful submissions. Here are the four key takeaways from this dynamic event. 1. Understanding the Importance of the Common Technical Document (CTD) One of the standout segments of the webinar focused on the Common Technical Document (CTD), a globally standardized format for regulatory submissions. Participants learned how the CTD facilitates organization.. READ MORE »

November 26, 2024

A male quality assurance expert at a manufacturing plant

Quality Assurance Webinar: Navigating the USP

Are you a quality assurance professional seeking to enhance your expertise in regulatory standards? Don’t miss our upcoming webinar on November 28, 2024! We’ll dive deep into the United States Pharmacopeia (USP), demystifying its complex structure and providing practical guidance for its effective use. Whether you’re a seasoned quality assurance reviewer, a quality control chemist, or a new science graduate, this webinar will equip you with the knowledge you need to navigate the USP confidently and accurately. Why Attend This Webinar? The USP is a critical resource for professionals across the pharmaceutical, cannabis, and herbal drug industries, setting standards to.. READ MORE »

November 19, 2024

A group of pharmaceutical professionals receiving cutting-edge training at our pharmaceutical institute.

Take Advantage of COJG: No-Cost Training Solutions for Your Team at AAPS

Canada’s commitment to building a highly skilled workforce includes the Canada-Ontario Job Grant (COJG), a valuable resource for pharmaceutical industry employers looking to invest in developing their teams. Through COJG, companies can access high-quality pharmaceutical training for their employees at our pharmaceutical institute, AAPS. This helps employers keep their teams at the forefront of industry standards. For pharmaceutical companies, COJG offers a cost-effective path to upskill employees, enabling teams to enhance their knowledge and adapt to the industry’s evolving needs. Here’s how this grant supports employer-driven team development. What is the COJG? The Canada-Ontario Job Grant (COJG) program provides financial.. READ MORE »

November 18, 2024

A female pharmaceutical QA professional at a manufacturing facility

Workshop for Pharma QA Pros: OOS Investigations for Testing Labs

Are you a pharmaceutical quality assurance professional seeking to strengthen your expertise in out-of-specification (OOS) investigations within testing labs? This critical area of QA can be challenging yet essential for ensuring product quality and regulatory compliance. Join us on November 14, 2024, for a comprehensive workshop on mastering OOS investigations explicitly designed for professionals like you. Why This Workshop Is Essential OOS results are a top priority for regulatory authorities. When test results fall outside predefined specifications, it’s not simply a “red flag” but a call for immediate and thorough investigation to maintain product integrity and regulatory compliance. Effective OOS.. READ MORE »

November 5, 2024

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