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 Advanced HPLC Certification Sep 14, 21, 28, Oct 5, 12, 19 | 9:30 AM - 3:30 PM (EST) (On Campus) Fundamentals of Data Integrity Sep 18 | 2:00 PM - 3:00 PM (EST) (Online) GMP Audits, Inspections, Preparation and Management Sep 19 | 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! LEARN MORE!

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Navigating CMC intricacies: Comprehensive Understanding in Our Workshop

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Greetings! We are excited to provide you with a more comprehensive overview of our upcoming event, Chemistry, Manufacturing, and Controls (CMC) Training, following our initial introduction. This webinar is meticulously designed to offer a profound understanding of the intricate world of CMC requirements, providing essential insights into the heart of the pharmaceutical industry. The virtual event is scheduled on October 10, 2024 between 9:00 AM to 5:00 PM (EST).   This webinar aims to unravel the complexities of the CMC portion of a Common Technical Document (CTD). Participants will engage in an in-depth analysis of critical topics, including the role of CMC in drug development, nomenclature and characterization of drug substances, analytical methods and validation, manufacturing processes, in-process controls, process validation, stability testing, and regulatory expectations for product characterization. Additionally, we will delve into the significance and structuring of Drug Master Files and explore the components integral to the CMC section in regulatory submissions. LEARN MORE Our webinar is tailored for professionals deeply involved in the pharmaceutical landscape, including directors, managers, supervisors, and associates engaged in various aspects such as regulatory affairs, quality assurance, product submission, training, consultancy, clinical research, documentation and technical writing, project management, and product development. Don't miss this opportunity to elevate your regulatory affairs knowledge and advance your career. Secure your spot today by registering online Date and Time: October 10, 2024 9:00 AM - 5:00 PM (EST) How is the webinar 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.

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Master Data Integrity for Only $99 – Limited Spots Available!

Join our expert-led online workshop and ensure your compliance with FDA data integrity requirements.

Greetings! In today’s regulated industries, maintaining data integrity is critical to ensuring compliance and safeguarding product quality. A single misstep can lead to severe consequences, ranging from product recalls to patient safety risks. That’s why we’re excited to offer our upcoming Fundamentals of Data Integrity webinar—an incredible opportunity for professionals to enhance their knowledge for only CAD $99.00! Our workshop will take place online on September 18, 2024, from 2:00 pm to 3:00 pm (EST). This session is designed to provide participants with a comprehensive understanding of data integrity principles and how to prevent data integrity issues. The focus will be on the key principles of ALCOA+, regulatory expectations, and an in-depth review of FDA warning letters. Attendees will gain actionable knowledge to develop compliant data integrity programs that safeguard their organization’s quality and compliance efforts. This is an incredible value for such in-depth industry knowledge, priced at just CAD $99.00. Led by our experienced instructors, this workshop will not only provide theoretical insights but also practical applications, including how to design systems that incorporate data integrity by design, preventing issues before they arise. Participants will leave the session with a clear understanding of how to comply with FDA data integrity requirements and how to apply that knowledge to their own organization. LEARN MORE If you want to elevate your expertise in data integrity and ensure compliance with regulatory standards, this is the workshop for you. The deadline to register is September 11, 2024, and all participants will receive a certificate of attendance upon completion of the workshop. Don’t miss this opportunity to strengthen your knowledge in this crucial area and enhance your professional skills. We look forward to seeing you at the workshop and helping you take your career to the next level. Date and Time: September 18, 2024 2:00 PM - 3:00 PM (EST) How is the webinar delivered? Live. Virtual. 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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LAST CHANCE: Early Bird 50% Off! Enhance Your Expertise with Our OOS Investigations Workshop

Register by September 6th to save 50% on our upcoming GMP environment workshop on September 12th.

Greetings! We are excited to announce a compelling opportunity for professionals in the pharmaceutical sector to enhance their expertise in managing Out of Specification (OOS) investigations in testing laboratories, a crucial aspect of Good Manufacturing Practice (GMP) environments. Join us for an enlightening online workshop, "OOS Investigations for Testing Laboratories in a GMP Environment," scheduled for Sep 24, 2024, from 1:00 pm to 5:00 pm (EST). Early Bird Special: Register by September 6th and receive 50% off! REGISTER TODAY! The session will not only cover the essentials of OOS but also introduce participants to Out of Trend (OOT) results, highlighting their significance in maintaining laboratory compliance and quality. With a focus on real-world applications, the workshop will explore FDA audit observations, elucidate the importance of robust quality support systems, and provide a step-by-step guide on conducting and reporting Phase 1 of OOS investigations. The dynamic presentation style, including a PowerPoint presentation, interactive exercises, and group discussions, ensures an engaging and enriching learning experience. Participants are encouraged to bring their own case examples to enhance the collaborative learning environment. LEARN MORE Designed for a diverse audience, this workshop is particularly beneficial for professionals in Quality Assurance, Quality Control Laboratory, Regulatory Affairs, and related fields in the pharmaceutical and associated industries. Attendees will walk away with not only a deeper understanding of OOS and OOT investigations but also practical strategies to implement corrective and preventative actions, minimizing future OOS results. As we strive to uphold the highest standards in our industry, continuous learning and professional development are key. We invite you to seize this opportunity to elevate your expertise and stay at the forefront of industry practices. Register online before the deadline on Sep 17, 2024, to secure your spot in this essential workshop. We look forward to welcoming you to this enriching learning journey and fostering a deeper understanding of OOS investigations that are pivotal to the pharmaceutical industry's success. Date and Time: Sep 24, 2024 1:00 PM - 5:00 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.

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