AAPS College of Health, Science and Technology

09/02/2026

Our Fall 2026 Student Networking Event is coming up, and we’d love to see our current AAPS students there.

It’s a chance to get out of the classroom for an evening, meet students and professors you may not usually cross paths with, chat with industry professionals, connect with Career Services, and have some genuinely useful conversations about where your career could take you.

We’ll also be joined by an industry keynote speaker. More on who that is very soon.

September 24 | 5:00–8:00 PM
AAPS Toronto Campus

And yes, there’ll be food, refreshments, and a few goodies too.

**If you’re a current AAPS student, keep an eye on your inbox for your invitation, or get in touch with us to register.**

09/01/2026

As fall begins, it can also be a good time to deepen your expertise in an area of your work that deserves a closer look.

Regulatory Affairs is rarely one discipline. It can involve clinical evidence, CMC, labelling, manufacturing requirements, post-approval obligations, and regulatory expectations that vary across products and markets.

AAPS offers individual courses across specialized areas of Regulatory Affairs, including:
• Introduction to Regulatory Affairs
• Pharma Regulatory Submissions, Labeling and Product Summaries
• Regulatory Affairs for Clinical Research and Preclinical Drugs
• Regulatory Affairs Biotech/Biologics
• Regulatory Affairs Medical Devices
• Regulatory Affairs Natural Health Products
• Post Approval Activities and Compliance
• Regulatory Affairs Generic Drugs
• Intellectual Property
• Chemistry, Manufacturing and Control
• Global Regulatory Affairs

Through September 30, individual Professional Regulatory Affairs courses are available at 50% off.

Visit aaps.ca to explore our Professional Regulatory Affairs program and individual courses, and learn more.

08/29/2026

What makes one batch of food taste, smell, and feel like the next? Discover how sensory evaluation helps quality teams measure appearance, aroma, flavour, and texture while supporting product consistency and development.

Discover sensory evaluation in food quality, which measures food appearance, aroma, taste, and texture to support product development.

08/25/2026

What does a strong drug submission look like when you move beyond the fundamentals?

In NDS Level 2: Practical CTD and eCTD Preparation for Drug Product Submissions, participants will take a closer look at the work behind advanced submissions, from CTD Modules 3, 4 and 5 and eCTD lifecycle management to regulatory queries, deficiencies and interactions with Health Canada.

Leading the workshop is AAPS Instructor Raymond Ho, a Regulatory Affairs professional whose experience spans pharmaceuticals, medical devices and natural health products. Raymond has led drug submissions through Health Canada and the FDA, including new and supplemental drug submissions, Drug Master Files and eCTD filings, bringing an industry-grounded perspective to the classroom.

For regulatory professionals, the difference is often in the details. This workshop goes there. Visit aapspharma.com/events to learn more

08/22/2026

Not every cybersecurity alert means an attack is underway. Discover how SOC analysts investigate security events, separate potential threats from false positives, and decide what needs attention first.

Learn how SOC alert triage helps cybersecurity analysts review security events, identify real threats, prioritize action, and reduce alert fatigue.

08/22/2026

How do pharmaceutical companies determine a medicine's expiration date? Learn how pharmaceutical stability studies help quality teams establish shelf life, storage conditions, and product safety.

Learn how pharmaceutical stability studies evaluate product quality over time and support shelf-life, storage, packaging, and regulatory decisions.

08/21/2026

A fresh look for a new chapter.

Our new AAPS College logo is officially up, marking another visible step forward as we continue to grow and evolve.

Same purpose. New identity. Onward.

08/19/2026

Amid the busy back-to-school season, we paused to celebrate two special milestones - a birthday and a wedding within the AAPS team.

Work continues; milestones remain. ✨

08/12/2026

AI in pharma has reached an interesting moment.

The conversation is no longer about whether Artificial Intelligence COULD transform drug development. It is about something far more important: what has it actually changed?

Where is the evidence? What is working in discovery, clinical trials, and safety today? What remains more promise than proof? And perhaps most importantly, how are regulators responding as the technology moves faster than the frameworks built around it?

These are questions we have been eager to explore through AAPS Pharma.

In ‘Proof, Not Promise: How AI Is Actually Changing Pharma’, we are bringing them together in an evidence-based session examining the real impact of Big Data and AI across pharma, the evolving FDA, EMA, and ICH regulatory landscape, and what professionals should be watching over the next 12 to 18 months.

There is an extraordinary amount of noise around AI right now. We are excited to create space for a different kind of conversation: one grounded in evidence, regulation, and what is actually happening in the industry.

Visit aapspharma.com/events to learn more

08/08/2026

Every successful clinical trial depends on more than scientific data; it also depends on accurate documentation. Learn why Trial Master Files are essential for regulatory compliance, participant safety, and study quality in our latest blog.

Explore the trial master file in clinical research and how accurate clinical research documentation supports compliance and study quality.