Friday, August 29, 2025

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

Discover the top events for you in our Weekly Event Guide


Out Of Specification (OOS) Investigations for Testing Laboratories in a GMP Environment

Sep11 | 1:00 PM - 3:00 PM (EST)

(Online)

Drug Product Submission (NDS) Preparation in CTD & eCTD Format Workshop- Level 1

Sep 26 | 3:00 PM - 5:00 PM (EST)

(Online)

GMP Audits, Inspections, Preparation and Management

Oct 2 | 1:00 PM - 3:00 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

Thursday, August 28, 2025

Strengthen Your Pharmaceutical Auditing Skills with Our Upcoming Workshop

Greetings!


Kickstart your journey in Regulatory Affairs with AAPS Pharma. This introductory workshop provides a clear, practical understanding of Regulatory Affairs in the healthcare industry, focusing on the drug development process and new drug submissions. Participants will explore the steps involved in obtaining drug approval, including notice types, priority review policies, and the importance of pre-submission meetings. The session also covers submission formatting and screening, highlighting the Common Technical Document (CTD) and the advantages of electronic CTD (eCTD) submissions. By the end of the workshop, attendees will have a strong grasp of the regulatory landscape and the essential components of drug submissions.


This workshop is ideal for individuals new to Regulatory Affairs or those seeking to strengthen foundational knowledge. It is particularly relevant for professionals in the pharmaceutical industry, including regulatory affairs specialists, drug development personnel, quality assurance staff, and anyone involved in the submission and approval of new drugs.


Participants will leave with the ability to understand regulatory submission requirements, navigate the new drug submission process, comprehend critical steps in drug development, and utilize CTD and eCTD effectively. Don’t miss this opportunity to gain practical, actionable insights that can advance your career in Regulatory Affairs.


Reserve your spot today and take the first step toward mastering Regulatory Affairs.

Date & Time

Sep 26, 2025

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

Wednesday, August 27, 2025

Strengthen Your Pharmaceutical Auditing Skills with Our Upcoming Workshop

Greetings!


Auditing contractors, vendors, and suppliers is more than a regulatory requirement—it is a cornerstone of pharmaceutical quality. Ensuring GMP compliance and strong Quality systems across external partnerships is critical to meeting regulatory expectations and protecting product integrity.


Our upcoming Pharmaceutical Auditing Workshop is designed to provide a practical, structured approach to audit readiness. Participants will gain a deeper understanding of audit fundamentals, planning, and performance, along with insights into data integrity, report writing, follow-up, and closure. The workshop also explores technical areas, including audits of classical chemical APIs, biological APIs, and dosage forms, ensuring you are prepared to navigate complex scenarios with confidence.


Led by experienced industry professionals, this program is tailored for quality assurance professionals, internal and external auditors, and Qualified Persons (QP) seeking to strengthen their auditing skills. Through real-world examples and interactive exercises, you will leave equipped to conduct audits effectively, manage compliance risks, and foster continuous improvement in your organization.


Join us for this essential workshop and build confidence in your audit processes- ensuring your teams and partners are always prepared, compliant, and audit-ready.


Register today to secure your spot.

Date & Time

Oct 2, 2025

1:00 PM - 3:00 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

Free Workshop: Introduction to the Role of a Quality Assurance Person (QAP) in Cannabis

Greetings!


We are pleased to invite you to a free workshop introducing the critical role of a Quality Assurance Person (QAP) in cannabis facilities. This session will provide participants with a clear understanding of the responsibilities, regulatory requirements, and best practices that guide quality assurance in the cannabis industry. Designed to highlight the importance of compliance, documentation, and adherence to Good Manufacturing Practices (GMP), the workshop will explore the key duties of QAPs, including batch release, product traceability, sanitation planning, recall and complaint systems, and maintaining quality standards throughout cultivation and processing operations. Attendees will gain valuable insights into the provisions of the Cannabis Act and Cannabis Regulations, particularly Good Production Practices (GPP) outlined in Part 5, and will learn how QAPs ensure product integrity by applying testing, documentation, and traceability measures.


This workshop is ideal for professionals aspiring to or currently working in Quality Assurance roles within the cannabis sector, as well as those in regulatory affairs, quality control, and compliance who wish to deepen their knowledge of QAP responsibilities. Through case-based discussions and practical examples, participants will explore common challenges and best practices in cannabis facilities, examine how to investigate deviations and recalls, and discover ways to foster a culture of compliance and quality across operations. By the end of the session, attendees will leave with a foundational understanding of the QAP’s role in ensuring product quality and safety, and practical strategies to apply within a professional setting.


Join us for this engaging and informative session and take the first step toward strengthening your expertise in cannabis quality assurance.

Date and Time:

Sep 4, 2025

1:00 PM - 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 416-502-2277 or email us at info@aaps.ca.

LinkedIn  Facebook  Instagram  Web  YouTube

Tuesday, August 26, 2025

Free Workshop: Introduction to New Drug Submissions (NDS)

Greetings!


The regulatory submission process for new drugs is a critical step in bringing innovative treatments to market. To help industry professionals, students, and those new to Regulatory Affairs understand the fundamentals of this process, AAPS Pharma is offering a free online workshop on the New Drug Submission (NDS) process.


This session provides an overview of Health Canada’s regulatory expectations, covering the Common Technical Document (CTD) structure, eCTD format, key documentation requirements, and the importance of pre-submission meetings. Participants will gain insights into the general steps of preparing and submitting an NDS and how regulatory submissions impact the pharmaceutical landscape.


Designed for individuals entering the field of Regulatory Affairs or those seeking to understand the basics of drug submissions, this workshop is particularly beneficial for professionals working in pharmaceuticals, healthcare, quality assurance, and drug development. Whether you are looking to advance your career or simply expand your knowledge, this session will equip you with the foundational skills needed to navigate the regulatory submission process.


Registration is open, and all participants will receive a certificate of attendance upon completion. Spaces are limited, so secure your spot today!

Date & Time

Sep 19, 2025

3:00 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 416-502-2277 or email us at info@aapspharma.com

LinkedIn  Web