Monday, March 23, 2026

For a Limited Time: 50% Off AAPS Recorded Webinars

Greetings!


In regulated industries, progress is often defined by moments that demand clarity.


A submission deadline. An inspection. A deviation that needs resolution. In those moments, preparation is not theoretical. It is decisive.


At AAPS College, we have supported professionals across pharmaceutical, regulatory, quality, clinical research, and cannabis sectors with training shaped by real regulatory expectations.


For a limited time, all on-demand recorded workshops are available at 50% off until March 31.


These sessions are built on practical insight from professionals who have worked through submissions, audits, validations, and regulatory transitions. The focus is simple. What works. What fails. And why.


Learn at your own pace, with content designed to be immediately applicable in regulated environments.


The standards will continue to evolve. The question is whether you will be ready.


This 50% sale ends March 31.

Interested to know more about AAPS College of Health, Science & Technology?

Register today by calling our team at 416-502-2277 or email us at info@aaps.ca.

Web  LinkedIn  YouTube  Facebook  Instagram

FINAL CALL: Master GMP-Compliant HPLC Testing

Greetings!


In highly regulated industries, precision is never optional. The safety, identity, strength, purity, and quality of products rely on the rigor of analytical testing and the integrity of documentation. High Performance Liquid Chromatography (HPLC) is at the heart of this effort, providing unmatched sensitivity and reproducibility in quantifying analytes across Pharmaceuticals, Cosmetics, and Food industries.


AAPS Pharma invites you to a half-day workshop that translates this complexity into clarity and actionable skill. Participants will explore the key components of HPLC systems, the preparation of mobile phases and samples, column selection, system suitability practices, and GMP documentation essentials. Attendees will also be introduced to Empower 3 software, gaining practical insight into data management in a GMP-compliant laboratory. By the end of this session, you will be equipped to execute HPLC testing with confidence, ensuring both accuracy and regulatory compliance.


This workshop is led by Kevin Mueller, a recognized leader in pharmaceutical analytical science with over 25 years of industry experience at Novopharm Ltd. and Teva Canada Ltd. Kevin has led teams across Analytical Research and Development, Quality Control, and Operational Excellence, bringing deep expertise in compliance, data integrity, laboratory investigations, and CAPA implementation. Known for his ability to motivate and guide professionals to reach their potential, Kevin combines technical mastery with practical insight drawn from decades of hands-on experience.


The workshop is designed for professionals with beginner to intermediate knowledge of GMP analytical testing using HPLC. It is particularly valuable for those working in Quality Control Laboratories, Analytical Research and Development, and Quality Assurance teams within Pharmaceuticals, Cosmetics, Food, or related industries.


To support your professional development, AAPS provides a certificate of attendance and a specially prepared course manual for every participant.


Take this opportunity to strengthen your technical expertise, ensure GMP compliance, and gain practical skills directly from an industry leader.

Date & Time

Mar 26, 2026

12:00 PM - 4:00 PM (EST)


How is the Workshop delivered?

Live. Virtual. Interactive. Instructor-led.

Interested in this workshop?

Register today by calling our team at 416-628-7575 or email us at events@aapspharma.com

LinkedIn  Web

Friday, March 20, 2026

Your Weekly Event Guide: Expand Your Learnings and Discover Exciting Opportunities

Discover the top events for you in our Weekly Event Guide


Accelerated HPLC Testing: 
What GMP Allows - And What It Doesn't

Mar 26 | 12:00 PM - 4:00 PM (EST)

(Online)

Natural Health Products (NHPs) Level 3 Workshop

Apr 17 | 11:00 AM - 2:00 PM (EST)

(Online)

NDS Submissions Explained: Where Applications Break Down

Apr 24 | 3:00 PM - 5:00 PM (EST)

(Online)


Are you ready to expand your learnings?


Broaden your knowledge and delve into new horizons with AAPS!


LinkedIn  YouTube  Facebook  Instagram  Web

NHP Level 3 is Here - Go Beyond Approval

Greetings!


Level 3 of our Natural Health Products workshop series moves beyond initial approval and into the ongoing regulatory responsibilities that govern products once they are on the market. Building on earlier sessions covering classification, licensing, manufacturing, and labelling, this workshop focuses on maintaining compliance across the full product lifecycle in Canada and beyond.


The session provides a practical overview of Canadian post-market requirements, including importation, exportation, and distribution. Participants will gain clarity on the responsibilities of licence holders, importers, and distributors, along with key exemptions for personal use and clinical trials. The workshop also introduces Master Files and their role in protecting proprietary ingredient information while supporting product licence and clinical trial applications.


A key focus is clinical trial oversight for NHPs. Attendees will learn when authorization is required, how trial phases differ, and what Health Canada expects in terms of applications, ethics approval, and adverse reaction reporting. The session also covers pharmacovigilance requirements, helping participants identify, assess, and report adverse reactions in line with regulatory expectations.


In addition, the workshop provides a comparative overview of international frameworks, including U.S. dietary supplement regulation under DSHEA and FDA oversight, offering insight into global compliance considerations.


This workshop is designed for professionals and students working with Natural Health Products and dietary supplements who need a practical understanding of post-market and global regulatory requirements. It is particularly relevant for those in regulatory affairs, quality assurance, product development, manufacturing, import/export, compliance, and clinical research roles.


The session is led by Andreea Simo, a regulatory affairs and quality professional with experience across global organizations such as PepsiCo and Jamieson Vitamins, as well as consulting firms and start-ups. Her background ensures a practical, industry-aligned understanding of how Natural Health Products are managed beyond approval and throughout their lifecycle.


Take advantage of our early bird discount by registering by March 27th. Use code SAVE20 while registering to save 20%.

Date & Time

Apr 17, 2026

11:00 AM - 2:00 PM (EST)


How is the Workshop delivered?

Live. Virtual. Interactive. Instructor-led.

Interested in this workshop?

Register today by calling our team at 416-628-7575 or email us at events@aapspharma.com

LinkedIn  Web

Wednesday, March 18, 2026

Hello, 20% off before March 25 for this NDS workshop

Greetings!


We are hosting a half-day workshop for professionals working in or alongside the drug submission process. If gaps in your regulatory knowledge are slowing you down, this session is worth your time.


The workshop covers the full New Drug Submission process - from drug development and notice types, through to submission formatting, priority review policy, and the Common Technical Document (CTD). A focused portion addresses eCTD submissions specifically, including where and why applications get screened out before they ever reach review.


It is particularly relevant for regulatory affairs specialists, drug development professionals, quality assurance personnel, and anyone involved in the preparation or filing of new drug submissions.


By the end of the session, you will have a clear, working understanding of what a compliant submission looks like, how the approval process is structured, and where most applicants go wrong. 

There’s an early-bird discount currently available for this event. If you register by March 25, you can save 20% by using the code SAVE20 at checkout.

Date & Time

Apr 24, 2026

3:00 PM - 5:00 PM (EST)


How is the Workshop delivered?

Live. Virtual. Interactive. Instructor-led.

Interested in this workshop?

Register today by calling our team at 416-628-7575 or email us at events@aapspharma.com

LinkedIn  Web