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X-ORIGINAL-URL:https://www.aaps.ca
X-WR-CALDESC:Events for AAPS
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DTSTART:20290101T000000
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BEGIN:VEVENT
DTSTART;VALUE=DATE:20290922
DTEND;VALUE=DATE:20390905
DTSTAMP:20260508T222935
CREATED:20190731T194254Z
LAST-MODIFIED:20260402T150648Z
UID:11038-1884729600-2198793599@www.aaps.ca
SUMMARY:Recorded Webinar – Good Production Practices (GPP) and Good Agricultural and Collection Practices (GACP) for the Cannabis Industry – Canada & Europe
DESCRIPTION:Recorded Webinar – Good Production Practices (GPP) and Good Agricultural and Collection Practices (GACP) for the Cannabis Industry – Canada & Europe	\n	\n		\n	 \n\n\n\nRecorded Webinar\nTime: 1.5 Hours\nCost: CAD$600+HST\n Buy Now!\n\n\n\n \nDescription\nIn order to ensure appropriate and consistent quality of medicinal/herbal substances\, it is necessary to establish good practices in growing\, harvesting\, and processing operations. Canada’s Access to Cannabis for Medicinal Products Regulations (ACMPR) requires Licensed Producers to implement and adhere to Good Production Practices (GPP). In Europe\, European Medicinal Agency (EMEA) requires adherence to Good Agricultural and collection Practices (GACP) for growing and harvesting. Both GACP and GPP are designed to ensure full traceability back to the seed source for each crop. Following GACP and GPP standards ensures that only the highest quality plants are grown and harvested. \nOutline\nACMPR – GPP \n\nAnalytical Tests\, Microbial and chemical contaminants and pest control products\nPremises\nEquipment\nSanitation Program – Premise\, Equipment\, Personnel\nStandard Operating Procedures\nRecall and Recall Reporting\nQuality Assurance\nRetained Samples\nAdverse Reactions and Adverse Reactions Reporting\n\nEMEA – GACP \nQA\nPersonnel and Education\nBuildings and Facilities\nEquipment\nDocumentation\nSeeds and Propagation material\nCultivation\nCollection\nHarvest\nProcessing\nPackaging\nStorage and Distribution
URL:https://www.aaps.ca/event/recorded-webinar-good-production-practices-gpp-and-good-agricultural-and-collection-practices
LOCATION:AAPS Training Center\, 200 Consumers Road\, Suite 200\, Toronto\, Ontario\, M2J 4R4\, Canada
CATEGORIES:Recorded Webinars
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BEGIN:VEVENT
DTSTART;VALUE=DATE:20290926
DTEND;VALUE=DATE:20390923
DTSTAMP:20260508T222935
CREATED:20190731T195457Z
LAST-MODIFIED:20260402T150203Z
UID:11057-1885075200-2200348799@www.aaps.ca
SUMMARY:Recorded Webinar – Review of the Safe Food for Canadians Regulations and Preventative Control Plan
DESCRIPTION:Recorded Webinar – Review of the Safe Food for Canadians Regulations and Preventative Control Plan	\n	\n		\n	\n\n\nRecorded Webinar\nTime: 2 Hours\nCost: CAD$600+HST\n Buy Now!\n\n\n\nCourse Overview\nThe Safe Food for Canadians Regulations (SFCR) came into force on January 15\, 2019. This course will provide guidance to the food industry on the regulatory changes introduced by the SFCR. At the end of the course\, participants will be able to understand the regulatory requirements that need to be met\, apply for licence\, identify and implement changes to company’s Preventative Controls to meet the Canadian Food Inspection Agency’s (CFIA’s) requirements. \nBenefit of the SFCR:\nFor trading partners abroad\, it means that they can continue to buy with confidence\, knowing that food produced in Canada meets internationally recognized safety standards. \nFor industry\, the SFCR’s outcome-based regulations mean innovation and the production of safer food. Businesses can better avoid costly recalls\, be more competitive at home and abroad\, and increase their growth potential by accessing an even greater number of international markets. \nCourse Outline\n\nWhat are the regulatory changes introduced by the SFCR?\nWhat is expected of the regulated parties/food industries?\nHow can the food industries meet the new regulations?\nWhich sectors are affected?\nWhat are the licensing requirements?\nHow to apply for licence?\nWhat are Preventative Control Plans (PCPs) and its elements?\nHow to meet traceability requirements under SFCR?\nUnderstand the requirements for Importers.\nUnderstand the requirements for Exporters.\nImplementation timelines for licensing\, PCPs and traceability\nCFIA’s new inspection model\n\nWho Should Attend\n\nAuditors\nConsultants to the food and cannabis edible industries\nPersonnel working in the food manufacturing\, processing\, import and export\nCannabis Edible industry\nOwners/Operators of Food Businesses\nFacility Managers & Directors\nFood Safety Personnel\nHACCP Team Members\nQA/QC Managers\, Technicians & Supervisors\nSupply Chain Managers
URL:https://www.aaps.ca/event/recorded-webinars-review-of-the-safe-food-for-canadians-regulations-and-preventative-control-plan
LOCATION:AAPS Training Center\, 200 Consumers Road\, Suite 200\, Toronto\, Ontario\, M2J 4R4\, Canada
CATEGORIES:Recorded Webinars
ATTACH;FMTTYPE=image/jpeg:https://www.aaps.ca/wp-content/uploads/img-featured-default.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20290930
DTEND;VALUE=DATE:20291001
DTSTAMP:20260508T222935
CREATED:20190731T195244Z
LAST-MODIFIED:20260302T172429Z
UID:11054-1885420800-1885507199@www.aaps.ca
SUMMARY:Recorded Webinar – Cannabis Micro Licence Application Process and Requirements
DESCRIPTION:Recorded Webinar – Cannabis Micro Licence Application Process and Requirements	\n	\n		\n	\n\n\nRecorded Webinar\nTime: 1.5 Hours\nCost: CAD$300+HST (50% off of $600 – limited time only)\n Buy Now!\n\n\n\nAbstract\nThe Cannabis Act establishes that an application for one of the Micro Cultivation/Processing Licence must be filed with Health Canada in the form and manner specified by the Minister and must include the information required by the Minister. \nAlthough security requirements are less demanding in comparison to obtaining a Standard Cultivation/Processing Licence\, the application process to acquire a Micro Licence under the Cannabis Act can still be complicated and requires undergoing a strict and thorough review by Health Canada. Applicants must ensure that the information provided in the application is detailed and accurate and clearly demonstrates that they are compliant with all the requirements of the Act. Insufficient or inaccurate information may give rise to grounds for refusal. Extensive details regarding the facility and its operations are required\, including: floor plan\, site and building information\, physical security requirements\, Good Product Practices (GPP)\, Standard Operating Procedures (SOP’s) Security Clearances\, notice to local authorities\, administrative forms and quality assurance reports. \nThis webinar discusses the application process including the form and manner for submitting an application for a Micro Licence and the information that is required to be submitted. \nCourse Outline\n\nBackground\nCannabis Micro Licence classes and subclasses\nCannabis Tracking and Licensing System (CTLS)\nApplication process and steps\nApplication documentation requirements\nKey positions\, site personnel and security clearances\nSite security plan\nOrganizational security plan\nSite & building information\nGood Production Practices (GPP) plan\nRecord keeping and reporting methods\nQA person\, master grower\, head of security\, head of client services\, SPIC\, RPIC\nNotices to the local authorities\nApproval process\nRefusal and withdrawals\nChanges to the application\nCurrent licences transitions – Equivalent licences under the Cannabis Act\nApplication costs and Cost Recovery Proposals – fees\n\nNote: Course outline is subject to change without notice. Please check back regularly for updates. \nWho Should Attend\nCannabis industry participants including employers and employees\, those who are interested in joining the industry\, licensed applicants\, and suppliers to the industry.
URL:https://www.aaps.ca/event/recorded-webinar-cannabis-micro-licence-application-process-and-requirements
LOCATION:AAPS Training Center\, 200 Consumers Road\, Suite 200\, Toronto\, Ontario\, M2J 4R4\, Canada
CATEGORIES:Recorded Webinars
ATTACH;FMTTYPE=image/jpeg:https://www.aaps.ca/wp-content/uploads/img-featured-default.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20290930
DTEND;VALUE=DATE:20391002
DTSTAMP:20260508T222935
CREATED:20190731T195714Z
LAST-MODIFIED:20250103T141249Z
UID:11062-1885420800-2201126399@www.aaps.ca
SUMMARY:Recorded Webinar – How to Write Effective Standard Operating Procedures (SOPs)
DESCRIPTION:Recorded Webinar – How to Write Effective Standard Operating Procedures (SOPs)	\n	\n		\n	\n\n\nRecorded Webinar\nTime: 2 Hours\nCost: CAD$600+HST\n Buy Now!\n\n\n\nAbstract:\nRegulatory Agencies require written procedures for all systems and operations which impact the quality and safety of pharmaceutical products. SOPs provide the main forum for the documentation of a Company’s systems\, processes and operations. SOPs are therefore the most popular documents audited by Regulatory Agencies during GMP inspections to ensure they reflect current practices that follow regulatory requirements and they are followed as written. \nEffective SOPs lead a company not only to consistency\, quality and compliance but also to executing efficient business operations. Often SOPs are written without consultation with the end user or by someone who has good writing skills but little experience of the topic. They can include too much information\, making them difficult to follow or too little detail causing them to be ambiguous. Such SOPs can lead to audit observations that the SOPs had not been followed or did not reflect current or acceptable practices. \nThis course is designed to provide helpful information and essential training towards achieving effective SOPs. It includes topics relevant to the writing\, formatting\, execution and management of SOPs and relates to the role which SOPs play in achieving the required level of compliance and quality.  \nCourse Outline\n\nWhat is an SOP?\nWhy do we need SOPs?\nWhen do we need SOPs?\nRoles and Responsibilities\nSections of an SOP\nWriting Tips\nHow SOPs are Written\nChange Control\nMaintenance\nSOP Workshop\n\nNote: Course outline is subject to change without notice. Please check back regularly for updates. \nWho Should Attend\nThis 2-hour webinar is targeted at anyone involved in the organization\, writing or management of SOPs required for GMP\, GPP\, GVP or GCP purposes.
URL:https://www.aaps.ca/event/recorded-webinar-how-to-write-effective-standard-operating-procedures-sops
LOCATION:AAPS Training Center\, 200 Consumers Road\, Suite 200\, Toronto\, Ontario\, M2J 4R4\, Canada
CATEGORIES:Recorded Webinars
ATTACH;FMTTYPE=image/jpeg:https://www.aaps.ca/wp-content/uploads/img-featured-default.jpg
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