Hi , want to avoid DATA INTEGRITY issues? Register today!

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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. Get Certified! LEARN MORE ABOUT THE WEBINAR IN DETAIL Follow us on Social Media to get regular news and updates!

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Hi , Learn How to avoid DATA INTEGRITY issues!

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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 Abstract: 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. This webinar focuses on principles of DI and how to manage DI issues and prevent recurrence. 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. Get Certified! LEARN MORE ABOUT THE WORKSHOP IN DETAIL Follow us on Social to get regular news and updates!

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Hi , do you know the Regulations for Cannabis Packaging and Labelling?

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Live Webinar: Health Canada’s Packaging and Labelling Requirements for Cannabis Products Greetings! This webinar examines Health Canada’s Packaging and Labelling requirements for different cannabis classes as well as different product forms. Gain practical understanding of the packaging and labelling requirements as well as how to avoid common mistakes and misinterpretations.   Who Should Attend? This course is designed for: Any individual with interest in Cannabis Regulatory Affairs, Quality Assurance, Product Development and Operations LEARN MORE Course Outline Cannabis classes and different product forms Health Canada Packaging requirements Health Canada labelling requirements Special considerations Packaging and Labelling examples: HC and Industry examples Common mistakes Packaging and labelling requirements for license amendments Q&A LEARN MORE     Date and Time: August 25, 2022 2:00 PM - 3:00 PM (EST) How is the webinar delivered? 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 , looking to get your Medical Devices approved? Learn the latest regulations here!

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Medical Devices Regulation in Canada - Principles and Recent Updates August 19th, 2022   Register Now! Workshop Details Time - 9:00 am - 5:00 pm Cost - CAD $645 + HST Location - Online. Live. Interactive. Instructor Led Abstract Medical devices companies who develop their products and wish to sell them in the Canadian market, must acquire knowledge of the Canadian regulatory requirements for medical devices. Moreover, in order to be able to commercialize their products, the manufacturer/importer/distributer must be aware of the new regulatory framework that Health Canada has developed for these products. The course will outline the main Canadian regulatory requirements for: ITA submission Licensing application Establishment of Quality Management Systems Risk management Who Should Attend Personnel involved with: Regulatory affairs Quality assurance Product development Manufacturing Clinical development Get Certified! LEARN MORE ABOUT THE WORKSHOP IN DETAIL Follow us on Social to get regular news and updates!

AAPS | 885 Sheppard Avenue West, Toronto, M3H 2T4 Canada Unsubscribe marnagianunzio59@gmail.com Update Profile | Constant Contact Data Notice Sent by newsletter@aaps.ca in collaboration with Try email marketing for free today!