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

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Discover the top events for you in our Weekly Event Guide Developing An Effective CAPA Strategy Jan 23 | 2:00 PM - 4:00 PM (EST) (Online) Chemistry, Manufacturing and Controls (CMC) Training Jan 30 | 9:00 AM - 5:00 PM (EST) (Online) Drug Product Submission (NDS) Preparation in CTD & eCTD Format Workshop – Level 2 Jan 31 | 2:00 PM - 4:00 PM (EST) (Online) Are you ready to expand your learnings? Broaden your knowledge and delve into new horizons with AAPS! LEARN MORE!

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Discover the World of Computer System Validation (CSV) – Don't Miss Out!

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Greetings! We are excited to invite you to a transformative learning experience that will unlock the potential of Computer System Validation (CSV) - Introduction to General Principles. The CSV module, a mandatory regulation from "Health Canada," the "Food and Drug Administration" (FDA), and the "European Union" (EU), ensures that computerized systems in the healthcare industry are validated for their intended use. Join us on February 20, 2025, from 1:30 pm to 4:30 pm (EDT) to delve into this critical aspect of the healthcare industry. Unravel the current regulatory requirements for computer system validation and understand the life cycle phases of system development. Acquire the skills to create, review, and approve essential validation deliverables, and learn how to maintain systems in a validated state. Moreover, grasp the audit requirements related to Computer System Validation and enhance your expertise in this vital domain. LEARN MORE! This module is tailor-made for professionals in healthcare, clinical trials, biopharmaceuticals, and medical devices. Whether you work in regulatory affairs, clinical research, marketing, or are an IT professional in the healthcare sector, this session will be invaluable for your career growth. Healthcare students aspiring to pursue validation as a career will also find this module enriching. Secure your spot for the CSV module by registering online. The deadline for registration is February 13, 2025. As we approach the event date, expect more exciting updates, sneak peeks, and special announcements about the CSV module. Our team is committed to making this learning journey unforgettable for you. Date and Time: Feb 20, 2025 1:30 PM - 4:30 PM (EST) How is the webinar delivered? Live. Interactive. Instructor-led. REGISTER TODAY! Interested in this webinar? Register today by calling our team at 416-502-2277 or email us at info@aaps.ca.

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Annual GMP Masterclass - Enroll Now and Elevate Your GMP Knowledge!

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Greetings! We are excited to announce the upcoming Annual GMP Masterclass, a comprehensive webinar that dives deep into the world of Good Manufacturing Practices (GMP) for pharmaceutical products. This event is scheduled for February 6, 2025, from 2:00 pm to 4:00 pm (EST), and it will be delivered virtually. The masterclass will cover the history, rationale, purpose, and GMP requirements related to pharmaceutical product manufacturing, packaging, labeling, testing, and control. Our expert instructors will guide you through the management responsibilities for GMP, principles of drug production, effective training requirements, and much more! Discover the significance of maintaining compliance in the pharmaceutical industry and the consequences of inaction. LEARN MORE! This program is perfect for professionals in various roles within the pharmaceutical, biopharmaceutical, vitamins, herbals, medical devices, and allied industries. Whether you're in Regulatory Affairs, Quality Assurance, Product Development, or any other area mentioned in the description, this masterclass is tailored to enhance your knowledge. Enroll today and equip yourself with the tools to assure quality in the workplace and drive success in your industry. Stay tuned for more updates and details in our upcoming newsletters. We can't wait to meet you at the webinar! Date and Time: Feb 6, 2025 2:00 PM - 4:00 PM (EST) How is the webinar delivered? Live. Interactive. Instructor-led. REGISTER TODAY! Interested in this webinar? Register today by calling our team at 416-502-2277 or email us at info@aaps.ca.

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DEADLINE APPROACHING FAST: Advance Your Regulatory Expertise – NDS Preparation Workshop (Level 2)

Elevate your expertise in CTD and eCTD formats

Greetings! We’re excited to announce our Level 2 workshop on New Drug Submissions (NDS) in CTD and eCTD formats, happening online on January 31, 2025, from 2:00 PM to 4:00 PM (EST). This advanced session is tailored to professionals aiming to deepen their regulatory expertise and master complex submission processes required by Health Canada. REGISTER TODAY! Whether you’re a regulatory affairs professional, quality assurance specialist, or someone involved in drug submissions, this Level 2 workshop offers invaluable tools to elevate your career. It’s also a great fit for professionals who have completed the Level 1 session or possess foundational knowledge of CTD and eCTD formats. Participants will gain hands-on knowledge of advanced regulatory requirements and practical skills to manage pre-submission meetings, respond to Health Canada inquiries, and ensure compliance. By the end of the session, you’ll be equipped with actionable strategies to excel in your field. LEARN MORE Registration closes on January 24, 2025, so don’t miss your chance to join this in-depth learning experience. All attendees will receive a certificate of completion. We look forward to helping you achieve your professional goals. Date and Time: Jan 31, 2025 2:00 PM - 4:00 PM (EST) How is the workshop delivered? Live. Virtual. Interactive. Instructor-led. REGISTER TODAY! Interested in this workshop? Register today by calling our team at 416-502-2277 or email us at info@aaps.ca.

AAPS | 885 Sheppard Avenue West | Toronto, ON M3H 2T4 CA Unsubscribe | Update Profile | Constant Contact Data Notice