Master Advanced CTD & eCTD Submissions – Level 2 Workshop

Build expertise in Health Canada NDS requirements, submission lifecycle, and regulatory strategies. Reserve your spot today.

Greetings! Advance your regulatory affairs expertise with AAPS Pharma’s upcoming Level 2 workshop on Drug Product Submission (NDS) in CTD and eCTD format. Tailored for professionals who have a foundational understanding of regulatory submissions, this training builds directly upon the concepts introduced in Level I, diving deeper into the technical and strategic elements of advanced Health Canada submissions. Through real-world case studies and in-depth guidance, participants will gain practical insight into Modules 3, 4, and 5, learning how to effectively handle quality documentation, nonclinical study reports, and clinical data. The workshop also focuses on how to manage the entire submission lifecycle—from conducting successful pre-submission meetings to addressing regulatory queries and navigating Health Canada’s expectations. Whether you’re working in regulatory affairs, clinical research, or quality assurance, this session will equip you with advanced tools and strategies to streamline your submission process. You’ll explore how to format documents for the eCTD platform, maintain compliance throughout the lifecycle, and leverage electronic submissions for efficiency and clarity. All attendees will receive a certificate of participation upon completion. Spaces are limited and registration will close one week prior to the event. We invite you to take the next step in your professional development and join a community of experts advancing pharmaceutical regulatory excellence. Ready to elevate your regulatory skillset? Date & Time May 2, 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@aapspharma.com

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Level 3 NDS Workshop Now Open — Advance Your Regulatory Skills!

Deepen your expertise in CTD/eCTD submissions and Health Canada compliance with AAPS Pharma.

Greetings! We’re excited to announce that Level 3 of our New Drug Submission (NDS) Training Series is now open for registration! Building on the advanced concepts covered in Level II, Level 3 takes you even deeper into the complexities of preparing New Drug Submissions (NDS) in CTD and eCTD formats for Health Canada. This workshop will focus on advanced dossier structuring, post-market submission requirements, detailed guidance on Health Canada's Module 1, and best practices for managing regulatory requests, including responses to Health Canada inquiries and reconsideration requests. This session is tailored for experienced regulatory affairs professionals, quality assurance specialists, and individuals managing complex submissions. If you have completed Level II or have significant experience with CTD/eCTD dossier preparation, this is your next step toward mastering regulatory filings and lifecycle management. Registration closes May 23, 2025 — don’t miss your chance to complete your NDS training journey with AAPS Pharma! If you have any questions, feel free to contact us at events@aapspharma.com. We look forward to continuing your professional growth journey! Date & Time May 30, 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 416-628-7575 or email us at info@aapspharma.com

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Build Your GMP Documentation Skills – Join Our Batch Record Review Workshop

Learn the fundamentals of batch record review and GMP compliance. Secure your spot in our Level 1 workshop today!

Greetings! AAPS is pleased to introduce Level 1 of our Batch Record Review Workshop, designed for professionals looking to build a solid foundation in Good Manufacturing Practices (GMP) and regulatory compliance. This essential session will introduce you to the key concepts of batch record review, including documentation requirements, production controls, and proper record-keeping techniques. Participants will gain practical knowledge on handling minor variances and discrepancies, ensuring compliance with GMP regulations and industry standards. Whether you're new to batch record review, part of a quality assurance or regulatory team, or working in pharmaceutical manufacturing, this workshop is an excellent starting point to develop your understanding of GMP documentation practices. Our expert instructor, Sudhanshu Sharma, will guide you through real-world examples and best practices to help you confidently review batch records and contribute to maintaining product quality. By the end of this workshop, you’ll be equipped with the essential skills to conduct accurate and compliant batch record reviews, ensuring product quality and regulatory adherence in your workplace. This knowledge will not only enhance your professional credibility but also support your career advancement in the pharmaceutical and healthcare industries. All participants will receive a certificate of attendance upon successful completion of the workshop. Date & Time May 15, 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@aapspharma.com

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Master HPLC in Just 2 Days – Certification Course at AAPS Pharma

Register Now!

Greetings! We are excited to present an intensive two-day certification course designed to equip professionals with the knowledge and technical proficiency required to master High Performance Liquid Chromatography (HPLC). Recognized as one of the most essential analytical techniques across the pharmaceutical, biotech, cannabis, food, and environmental industries, HPLC plays a critical role in separating, purifying, and quantifying organic compounds with precision. Through expert-led, hands-on training in a GMP-compliant lab environment, participants will gain practical skills using state-of-the-art instrumentation and software. From system setup and method development to data analysis and regulatory compliance, this course ensures a comprehensive understanding of both the theory and real-world application of HPLC. Ideal for professionals working in Quality Control (QC), R&D, and analytical lab settings, this program prepares attendees to navigate the technical and regulatory demands of modern laboratory operations. Participants will be guided through core areas including sample preparation, mobile phase creation, system suitability testing, and operation of Agilent systems using Empower 3 software. The knowledge gained during the certification course is directly transferable to day-to-day lab functions, ensuring immediate impact in both performance and confidence. Whether you are a QC analyst, technician, manager, or involved in method validation and documentation, this course is tailored to deepen your expertise and reinforce your understanding of HPLC systems. Upon completion, each participant will receive a certificate of attendance, recognizing their professional development and commitment to excellence in laboratory practice. Seats are limited, and registration closes one week prior to the course start date. Individual registration is required, and group rates are available upon request. If you are ready to advance your skills and strengthen your technical profile in one of the most in-demand laboratory techniques, we welcome you to join us. Date & Time May 3-4, 2025 9:30 AM - 4:30 PM (EST) How is the Course delivered? On-site. Interactive. Instructor-led. REGISTER TODAY Interested in this Course? Register today by calling our team at 416-502-2277 or email us at info@aapspharma.com

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Unlock New Skills with Our $99 Cannabis Workshop – Register Now!

Register TODAY!

Greetings! We’re excited to invite you to our upcoming workshop on Navigating Brands, Pricing, and Sales Strategies in the cannabis industry! For just $99 CAD, you’ll gain essential knowledge to advance your career in cannabis retail. This workshop is designed to give you a comprehensive overview of the cannabis corporate landscape, focusing on the strategies that will empower budtenders and sales associates to make well-informed product recommendations based on consumer needs. Whether you're new to the industry or looking to sharpen your skills, this session will provide valuable insights into navigating licensed producers, pricing strategies, and building rapport with customers to enhance your sales approach. Participants will learn about the differences between craft and mass-produced cannabis, pricing tiers, and how to make tailored recommendations that resonate with customers’ preferences and budgets. By the end of the workshop, you will be equipped with the tools to foster trust with customers, promote repeat business, and effectively upsell products. Don’t miss this opportunity to enhance your knowledge and boost your career! Register now to secure your spot. All participants will also receive a certificate of attendance upon completing the workshop. Looking forward to seeing you there! Date & Time April 25, 2025 1:00 PM - 3:00 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@aapspharma.com

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