Looking for a GMP refresher? Get certified training here.

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GMP Fundamentals Webinar Curious about how Good Manufacturing Practice can help you in making informed decisions to improve your strategy and return on investment?  Don’t miss our Live Webinar GMP Fundamentals! You will gain practical knowledge in understanding the essential elements and quality systems required for GMP and for maintaining compliance in the pharmaceutical industry. Who Should Attend? Directors, Managers, Supervisors, Associates in the Pharmaceutical, Biopharmaceutical, Vitamins, Herbals, Medical Devices, etc.  LEARN MORE  Course Outline Assuring Quality in the workplace The benefits of GMP compliance Management Responsibilities for GMP SISPQ/principles of drug production AND MORE...   Date and Time: June 01, 2023 2:00 - 4:00 PM (EST) How is the webinar delivered? Online, Live, Interactive, Instructor-led GET CERTIFIED TODAY! We hope you'll be joining us to begin your journey to land your dream job! Start your application by calling our enrollment team at 416-502-2277 or sending us a direct inquiry at info@aaps.ca Academy of Applied Pharmaceutical Sciences

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Everything You Need to Know About Pharmaceutical Drug Formulation!

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Greetings! Pharmaceutical drug products come in a variety of dosage forms and comprise of distinct formulations manufactured according to specific processing instructions.  Formulation scientists develop pharmaceutical products in conjunction with specialists in other disciplines such as pharmacokinetics, pharmacology, toxicologists, clinicians and others to ensure the final product is safe, effective and of the highest quality. Registration Deadline: May 2nd, 2023 REGISTER NOW!   The following topics will be covered during the Workshop: Introduction to pharmaceutical formulation and manufacturing API properties that influence formulation Common excipients used to formulate drug products Basics of formulating a drug product Immediate release Controlled release Formulating tablets Manufacturing tablets Formulating liquids Manufacturing liquids Formulating semi-solids Manufacturing semi-solids Overview of some specialty dosage forms LEARN MORE! Date and Time: May 09, 2023 9:00 AM - 5:00 PM (EST) How is the webinar delivered? Online. Live, Interactive, Instructor-led Get Certified 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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Coming in just 2 weeks! - Don't Miss Out & Get Your Tickets NOW to the State of Pharma Conference!

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Exciting news! Only 2 weeks to go for the State of Pharma (SoP) conference. This premier interdisciplinary event is just around the corner. Explore the latest trends, discover breakthrough innovations, and network with top industry leaders at our highly anticipated event. Spaces are filling out fast, don't miss out on this unforgettable opportunity to expand your knowledge, build valuable connections, and shape the future of pharma. Register Today! Clinical Trial Design and Alternative Data Sources (e.g. Diversity, real-world data, precision medicine and patient-focused drug development) Adam will discuss:  How to leverage different types of source documents. How to use hybrid trial methodology that combines traditional randomized controlled trials (RCTs) and observational study designs. How to apply alternative designs such as cross-over and n-of-1 trials, enriched enrollment, randomized withdrawal design, and adaptive designs. Whether you are a novice or an expert in clinical trial design, you will benefit from this session that will help you enhance your evidence-based practice using real-world data. TICKETS       BUY NOW       GROUP TICKETS (50% DISCOUNT)       BUY NOW

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Gain in-depth knowledge of Chemistry, Manufacturing and Controls (CMC)

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REGISTRATION ENDS TOMORROW Greetings! The objective of this course is to provide a strong understanding of the importance and underlying principles for CMC requirements from the regulatory perspective. Participants will gain an understanding of the CMC portion of a Common Technical Document (CTD) which is the format that regulatory submissions in Canada and the EU must be filed. Registration Deadline: April 28th, 2023 LEARN MORE Course Outline The following specific topics will be addressed in detail: Role of CMC in drug development Nomenclature and characterization of drug substance Analytical methods and validation Manufacturing, in-process controls and process validation Developing drug substance and drug product specifications Stability, stability-indicating tests and how much change is acceptable Regulatory expectations for product characterization Drug Master Files Structure, content and components relating to CMC section of a regulatory submission LEARN MORE Date and Time: May 05, 2023 9:00 AM - 5:00 PM (EST) How is the webinar delivered? Online. Live, interactive, instructor-led GET CERTIFIED TODAY! Interested in this workshop? Register today by calling our team at 416-502-2277 or email us at info@aaps.ca. Academy of Applied Pharmaceutical Sciences

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