Hi , How to classify and report ADEs? Find out today!

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Drug Safety and Adverse Drug Reaction Reporting Workshop September 19, 2022 Register Now! Workshop Details Time - 9:00 am - 5:00 pm Cost - CAD $645 + HST Location - Online. Live. Interactive. Instructor Led Abstract: This workshop will explain the importance of adverse drug reactions, the Canadian MedEffect Scheme, the source of adverse drug reaction reports and the differences between serious and non-serious events. In addition, a MedEffect form will be completed in class. Course Outline On completion of this workshop students should be able to: explain the importance of adverse drug reaction reporting explain the importance of the Canadian MedEffect system understand the source of safety reports explain how the safety reporting Scheme works differentiate between serious and non-serious ADRs and identify when completion and submission of MedEffect forms is required complete a MedEffect form   Certificate of Attendance and Course Material All participants will receive a certificate of attendance upon completion of the course. The participants will be receiving specially prepared course manual. Get Certified! LEARN MORE ABOUT THE WORKSHOP IN DETAIL Follow us on Social Media to get regular news and updates!

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LAST CHANCE TO REGISTER! Live Webinar Data Integrity Key Considerations

Live Webinar Data Integrity Key Considerations August 23rd, 2022 Register Now! Workshop Details Time - 2:00 pm - 4:00 pm Cost - CAD $350 + HST Location - Online. Live. Interactive. Instructor Led Data integrity is a key component in making informed decisions within any regulated organization. Reliable data promotes good decisions. Unmanaged and inaccurate data will have consequences on a company’s quality output, state of compliance, the risk to patient safety, and ultimately, the bottom line. There are many risks inherent in poor data management. Without the ability to eradicate these risks, gaps will inevitably exist and a quality system will not reach a reliability level that government agencies such as the FDA, expect to see. Ensure your data integrity program is compliant. Develop a strategy after getting the information you need in this live webinar. Course Outline What is Data Integrity and why is it important? Regulatory Background Types of Data Integrity Key principles of Data Integrity and ALCOA+ Elements of Data Integrity Leading causes of Data Integrity failures Evaluating Data Integrity Compliance How to comply with FDA Data Integrity requirements? Data Integrity by Design Data Integrity and automated systems Data Integrity most common root causes and how they can be addressed? FDA warning letters and 483s related to Data Integrity Data Integrity and cGMP Current Data Integrity trends in Pharmaceutical Industry Case Studies Who Should Attend This webinar is intended for anyone involved with Quality Assurance in Pharmaceuticals, Food, or Cannabis. LEARN MORE ABOUT THE WEBINAR IN DETAIL Follow us on Social Media to get regular news and updates!

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Hi , Plan, Perform and Host Pharmaceutical and Regulatory Audits

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Introduction to Pharmaceutical Auditing Techniques Workshop Greetings! Auditing of contractors, vendors, and suppliers in the Pharmaceutical industry is not only a regulatory requirement but also a critical Quality practice. Companies are outsourcing more and more of their capabilities to outside experts but the importance of establishing the GMP compliance and Quality systems status of these parties has been undervalued. Many companies fail to appreciate that all their contractors, vendors and suppliers are an extension of their own company and must therefore be held to the same standard that’s expected of them. This is accomplished through effective auditing. Effective and consistent auditing assures a company’s network of external contractors and vendors is at the level of quality required. The result is not only compliance with regulations but also reduced rejects, less problems, and fewer complaints. In the end it helps assure only products of the highest quality are provided to the patient. These auditing principles are equally applicable to internal audits.  LEARN MORE   Course Outline This workshop will introduce students to: The basics of auditing Audit planning Conducting audits Effective auditing techniques Audit analysis tools Writing audit reports Audit follow-up and closure LEARN MORE Date and Time: September 02, 2022 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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Hi , want to analyze your samples with HPLC?

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HPLC School Cannabis, Pharmaceutical and Food  SEP 12-23, 2022 Register Now! Workshop Details Time - 5:00 pm - 9:00 pm Cost - CAD $1595 + HST Location - In-Person. Live. Interactive. Instructor Led (AAPS Training Center - 885 Sheppard Ave W, Toronto, Ontario, M3H 2T4) High Performance Liquid Chromatography (HPLC) is an analytical technique for separating organic compounds in order to analyze their properties. HPLC is utilized in many industries such as biological, pharmaceutical, food, environmental and cannabis to analyze samples. HPLC is a very popular instrument for compound analysis since it is simple to learn and easy to use. Modern HPLC are applied in quality control (QC) and research and development (R&D) to separate, identify, purify and quantify compounds. In the pharmaceutical industry, it is commonly used to quantify the active pharmaceutical ingredient (API) or label claim (LC). In the cannabis industry, HPLC is the primary instrument to determine %THC, %THCA, %CBD and %CBDA. The HPLC training certificate program at AAPS prepares students by providing hands-on practical skills necessary to perform HPLC analysis. Course Outline Introduction to High Performance Liquid Chromatography (HPLC) principles Preparation of mobile phase, samples and standards Perform system suitability analysis Column setup and troubleshooting HPLC identification, assay and impurities tests Operations of Agilent and Waters HPLC system Navigation through Millennium (Empower) and ChemStation software Introduction to method validation and technology transfer Who Should Attend This course is intended for those who are interested in operating HPLC; as a technician, analyst or managers looking to work or setup an analytical laboratory. No previous laboratory experience is required for this workshop. Completing a HPLC Training certificate program at AAPS means that a wide range of careers in the pharmaceutical, food and cannabis industry will can be available. Employers in every sector know that they can count on the experience and skills of AAPS graduates for positions including: Pharmaceutical Laboratory Technician Quality Control and Assurance Analyst Medical Manufacturing Quality Control Manager Analytical Chemist Associate Scientist Research Quality Control HPLC Analyst  Certificate of Attendance and Course Material All participants will receive a certificate of attendance upon completion of the course. The participants will be receiving specially prepared course manual. Registration Fee Includes Presentation materials, laboratory equipment, lab coats, safety glasses, chemical reagents and free parking. Get Certified! LEARN MORE ABOUT THE WEBINAR IN DETAIL Follow us on Social Media to get regular news and updates!

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