Meet the Expert Instructor for our CAPA Strategy Workshop!

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Greetings! We are thrilled to introduce you to Mr. Rany Attalla, the esteemed instructor for our upcoming workshop on "Developing an Effective CAPA Strategy". With over two decades of profound experience in the Pharmaceutical industry, Rany brings a wealth of knowledge and expertise to our event. Our webinar, scheduled for March 7, 2024, from 10:00 am to 12:00 pm (EST), delves into the critical role played by Quality Assurance professionals in identifying and addressing deviations from standard operating procedures and regulatory requirements.   Certifications: Rany is a certified Quality Auditor from the American Society for Quality (ASQ) and a Lead Auditor (TPECS) from the British Standards Institution (bsi). Additionally, Rany is a Certified Black Belt Lean Six Sigma from Aveta Business Institute, USA, underlining his commitment to excellence and quality improvement. Professional Experience: Throughout his career, Rany has served as a Pharmaceutical Quality and Compliance Manager in various Multinational Pharmaceutical companies. He has also excelled as an Independent GMP & Auditing Consultant, demonstrating his versatility and expertise in diverse roles. LEARN MORE Rany's wealth of knowledge and practical insights make him an invaluable resource for our workshop participants. Don't miss this opportunity to learn from a seasoned expert who has successfully navigated the complexities of the Pharmaceutical industry. Date and Time: March 7, 2024 10:00 AM - 12:00 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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Experience AAPS - Join Our Open House Event! 🧪🔬

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Greetings! We're thrilled to announce that on March 6th, 2024 the Academy of Applied Pharmaceutical Sciences (AAPS) will be opening its doors to the public! Join us for an exclusive Open House event and take the first step towards your future in the pharmaceutical sciences. The timings for the event will be 3-7 PM (EST). Meet the Minds Behind AAPS Get a chance to interact with our esteemed faculty members and gain insights into the innovative learning environment that makes AAPS a leader in pharmaceutical sciences education. Tour Our State-of-the-Art Campus Explore our modern facilities, cutting-edge labs, and comfortable learning spaces where you can envision yourself mastering your craft. Learn About Our Programs Receive detailed information about our diverse range of programs and find the path that's perfect for you, from Quality Control to Clinical Research and more. Why Attend? Network with industry professionals and faculty Experience the AAPS community and culture Engage in one-on-one discussions about your educational aspirations Enjoy light refreshments and a warm atmosphere Spaces are limited, so don't miss out on this opportunity to step into a world of possibility and advancement. Your journey in the pharmaceutical sciences begins here, at AAPS. We look forward to welcoming you! Secure Your Spot Now Interested to know more about AAPS? Register today by calling our team at 416-502-2277 or email us at info@aaps.ca.

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Hello, Deep Dive into Data Integrity: Enhance Your Compliance and Quality Assurance

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Greetings! In our continuous effort to empower professionals within regulated industries, we are delighted to offer a deeper insight into our upcoming webinar: Data Integrity and Good Documentation Practices (GDP) for Reviewers. This pivotal event, scheduled for March 21, 2024, from 2:00 pm to 4:00 pm, promises to be an enlightening session that aims to fortify the foundations of data integrity and documentation practices within your organization. Data integrity forms the cornerstone of informed decision-making in any regulated environment. The accuracy and management of data directly impact a company's quality output, compliance status, patient safety, and financial health. Recognizing the critical challenges and risks associated with poor data management, this webinar is designed to address the gaps that may compromise the reliability of a quality system. Such gaps are often scrutinized by regulatory authorities, including the FDA, which mandates that all data be reliable and accurate. LEARN MORE This webinar is tailored for professionals involved in Quality Assurance across various sectors, including Pharmaceuticals, Food, and Cannabis. It represents an invaluable opportunity to develop a comprehensive understanding of DI and GDP, ensuring your data integrity program is compliant and equipped to support informed decision-making. We invite you to register online before the deadline on March 14, 2024, to secure your participation in this crucial webinar. Join us to elevate your knowledge and strategy in Data Integrity and Good Documentation Practices, and take a significant step towards enhancing your organization's compliance and quality assurance efforts. Date and Time: March 21, 2024 2:00 PM - 4:00 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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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 April 12, 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: April 12, 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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