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X-WR-CALDESC:Events for AAPS
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TZID:America/Toronto
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TZNAME:EDT
DTSTART:20220313T070000
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DTSTART:20221106T060000
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BEGIN:VEVENT
DTSTART;TZID=America/Toronto:20220120T080000
DTEND;TZID=America/Toronto:20220120T170000
DTSTAMP:20260430T074517
CREATED:20220120T060819Z
LAST-MODIFIED:20220120T060819Z
UID:20443-1642665600-1642698000@www.aaps.ca
SUMMARY:Live Webinar Cannabis Extraction – Ethanol/Alcohol
DESCRIPTION:Live Webinar Cannabis Extraction – Ethanol/Alcohol	\n	\n		\n \n\n\nAbstract\nCannabis Extraction is a method of selective separation of cannabinoids and other desired compounds from the plant matter using physical or solvent related methods. One of the most popular solvents used for extraction is ethanol. It has a long history of tincture use and is the foundation of most cannabis derivatives we see today.   \nWith a focal point on ethanol procedures\, this workshop will guide the attendee through the solvent extraction processes\, the infrastructure requirements\, and how to properly use and store this compound. \nHere you will: \n\nAcquire knowledge of how ethanol is produced and what makes it an efficient solvent\nGain understanding of temperatures surrounding extraction and what compounds are desirable\nVisualize post processes such as filtration\, solvent recovery\, colour remediation\, and final packaging\n\n \nCourse Outline\n\nEthanol source\, storage and other operational considerations\nSolvent extraction using ethanol and filtration \nTemperature considerations regarding solvent extraction \nExtraction equipment and basic procedure \nSolvent recovery devices \nFlashpoints \nCo-solvent extraction \n\nNote: Course outline is subject to change without notice. Please check back regularly for updates. \n\nWho Should Attend\nThis course is intended for those who are enthusiastic about alcohol solvent extraction\, either as someone who would like to gain insight on this aspect of their business or to gauge whether extractions could be a potential career option. The course covers a wide and general overview of extraction sciences\, and as such\, no previous scientific background is required.
URL:https://www.aaps.ca/event/live-webinar-cannabis-extraction-ethanolalcohol
CATEGORIES:Live Webinars
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Toronto:20220120T080000
DTEND;TZID=America/Toronto:20220120T170000
DTSTAMP:20260430T074517
CREATED:20220120T060331Z
LAST-MODIFIED:20220120T060331Z
UID:20440-1642665600-1642698000@www.aaps.ca
SUMMARY:Live Webinar Cannabis Extraction – Hydrocarbon
DESCRIPTION:Live Webinar Cannabis Extraction – Hydrocarbon	\n	\n		\n \n\n\nAbstract\nCannabis Extraction is a method of selective separation of cannabinoids and other desired compounds from the plant matter using physical or solvent related methods. Hydrocarbons\, and their ability to capture authentic terpene profiles makes them the backbone of most concentrate derivatives. \nWith a focus on butane extraction\, this workshop will guide the attendee through the hydrocarbon extraction processes\, the infrastructure requirements\, and the vast range of end products that can be created. \nHere you will: \n\nLearn how hydrocarbon’s chemical structure makes it a desirable solvent\nGain understanding of regulations surrounding infrastructure and safety\nStudy hydrocarbon components\, systems\, and how they operate \n\n \nCourse Outline\n\nHydrocarbons – Different types of Alkanes \nInfrastructure Requirements – Class 1 Division 1\nPPE and Safety regulations \nButane Extraction Components and basic procedure\nFinal products of hydrocarbon extraction \n\nNote: Course outline is subject to change without notice. Please check back regularly for updates. \n\nWho Should Attend\nThis course is intended for those who are enthusiastic about hydrocarbon extraction\, either as someone who would like to gain insight on this aspect of their business or to gauge whether extractions could be a potential career option. The course covers a wide and general overview of extraction sciences\, and as such\, no previous scientific background is required.
URL:https://www.aaps.ca/event/live-webinar-cannabis-extraction-hydrocarbon
CATEGORIES:Live Webinars
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Toronto:20220120T080000
DTEND;TZID=America/Toronto:20220120T170000
DTSTAMP:20260430T074517
CREATED:20220120T055137Z
LAST-MODIFIED:20230119T202922Z
UID:20437-1642665600-1642698000@www.aaps.ca
SUMMARY:Live Webinar Cannabis Extraction – Supercritical CO2
DESCRIPTION:Cannabis Extraction: Common Techniques	\n	\n		\n \n\n\nAbstract\nCannabis Extraction is a method of selective separation of cannabinoids and other desired compounds from the plant matter using physical or chemical techniques. Many types of extraction exist\, although CO2 extraction is one of the most used due to its environmental approach and reliability. \nWith special focus on solventless procedures\, this workshop will guide the attendee through the extraction processes found in a typical LP\, from the milling of the plant material to the final formulated product. Here you will: \n\nLearn about extraction technologies and a summary of each type\nLearn about subcritical & supercritical phases of CO2 and its use as an extraction solvent\nPerform a simulation of common extraction processes\, such as weighing and preparing concentrated cannabinoid samples for HPLC preparation\, and other downstream post-extraction processes\n\n \nCourse Outline\n\nAnatomy of cannabis and how it relates to extraction \nExtraction technologies and a summary of each type\nSubcritical & Supercritical phases of CO2 and how they are different \nExtraction principles such as polarity\, solubility\, and viscosity \nExtraction equipment and their role in the extraction process\nSafety and good production practices in your role as an extraction technician\, including labeling conventions of chemical items in the laboratory\nPrerequisite steps prior to extraction and downstream processes post extraction\n\nNote: Course outline is subject to change without notice. Please check back regularly for updates. \n\nWho Should Attend\nThis course is intended for those who are enthusiastic about solventless and C02 extraction\, either as someone who would like to gain insight on this aspect of their business or to gauge whether extractions could be a potential career option. The course covers a wide and general overview of extraction sciences\, and as such\, no previous scientific background is required.
URL:https://www.aaps.ca/event/live-webinar-cannabis-extraction-supercritical-co2
CATEGORIES:Live Webinars
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20200505T140000
DTEND;TZID=UTC:20200505T160000
DTSTAMP:20260430T074517
CREATED:20190730T234544Z
LAST-MODIFIED:20230119T200235Z
UID:10909-1588687200-1588694400@www.aaps.ca
SUMMARY:Live Webinar Lean for Root Cause Analysis & Corrective Action
DESCRIPTION:Developing an Effective CAPA Strategy	\n	\n        \n		\n	\n\n\n\n\nCourse Overview\nA key role for Quality Assurance professionals is identifying and addressing deviations from standard operating procedures and regulatory requirements. In order to effectively prevent recurrence of the events\, it is very important to correctly identify and address the underlying root causes. This not only involves dealing with specific incidents but also taking a holistic view of the process to ensure that it is fundamentally sound and is designed in such a way as to minimize the occurrences of deviations. This workshop will leverage Lean principles to get beyond the common root cause identification of “human error”. The tools and techniques presented in this course can be applied to everyday work to make processes simpler and reduce the time and effort required to complete daily tasks. \nCourse Outline\n\nIntroduction to Lean\nEssentials for Good  Processes  (5 Principles of Lean)\nIdentifying Non-Value Added Activities (8 Wastes of Lean)\nLean Problem Solving Methodology\nEffective Problem Definition\nRoot Cause Identification\nProcess Mapping\nCorrective Action Development\nConfirmation of Results\n\nNote: Course outline is subject to change without notice. Please check back regularly for updates. \nWho Should Attend\nThis one-day course is valuable for Directors\, Managers\, Supervisors\, Associates in the Pharmaceutical\, Biopharmaceutical\, Vitamins\, Herbals\, Medical Devices and allied industries with daily responsibilities in the following areas: \n\nQuality Assurance\nRegulatory Affairs\nOperations\nTraining & Development\nDocumentation and Technical Writing\nProject Management
URL:https://www.aaps.ca/event/live-webinar-lean-for-root-cause-analysis-corrective-action
CATEGORIES:Live Webinars
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20200327T140000
DTEND;TZID=UTC:20200327T153000
DTSTAMP:20260430T074517
CREATED:20190731T004018Z
LAST-MODIFIED:20200408T001730Z
UID:10939-1585317600-1585323000@www.aaps.ca
SUMMARY:Live Webinar Optimization of a Pharmaceutical Granulation Process using Quality by Design (QbD)
DESCRIPTION:Live Webinar Optimization of a Pharmaceutical Granulation Process using Quality by Design (QbD)	\n	\n		\n	Register online \n\n\nDates Available\nMay 22\, 2020 \nTime\n2:00 p.m – 3:30 p.m. \nCost\nCAD $345.00 + HST \nLocation\nOnline Webinar \nDistinguished Faculty\nAndy Tallevi Formulation/Process Consultant\nKeller Consulting \n\n\nAndy Tallevi is a Formulation/Process Consultant for Keller Consulting in Mississauga\, Ont.\, Canada. He has 28 years of industrial experience\, primarily in the Pharmaceutical industry. He currently consults clients in the Pharma and chemical industries assisting them with formulation and process issues and is an instructor at AAPS. \nMost recently Andy spent 1 year with Health Canada in the Bureau of Pharmaceutical Sciences reviewing and evaluating generic submissions and making recommendations for approval or refusal of Notice of Compliance for the Bureau. He has gained significant insights to the regulatory requirements and expectations of the drug substance and drug product sections of a submission filing to Health Canada. In addition\, he has an excellent understanding of the regulatory requirements for pharmaceutical development\, the GMP requirements expected for pharmaceutical manufacture and has assisted former employers numerous times in audits by Health Canada and the FDA. \nPrior to this\, Andy worked as a Senior Pharmaceutics Scientist for GlaxoSmithKline in Canada. During his 18 years with the company he led many projects developing new chemical entities in varying dosage forms. His specialty is solid oral dosage forms. He and his team successfully formulated immediate release tablets as well as many controlled release versions of GSK new chemical entities. He has experience with conventional matrix approaches as well as proprietary technologies such as Procise® and DiffCORE®. He has been responsible for overseeing the manufacture of clinical supplies of NCEs both in Canada and at other GSK sites in Europe and the US. \nAndy also has a solid understanding of material properties required of excipients and actives for successful formulation and for robust processes. He is well versed on particle sizing and powder flow. He holds a US patent on a novel approach for the assessment of the flow of pharmaceutical powders. \nPrior to leaving GSK he was heavily involved in a company-wide effort to strengthen its processes by Design for Manufacture through the use of PAT and experimental design for which he was the lead user in Mississauga. \nPrior to GlaxoSmithKline Andy worked as a scientist for Unilever developing products in the health\, beauty and detergent industries. He graduated from the University of Toronto with a B.Sc. major in Chemistry. \nAndy lives in Mississauga with his wife and 2 children. \nCourse Overview\nFor many years pharmaceutical companies have placed considerable effort in developing robust manufacturing processes to assure the highest quality products\, minimize defects\, eliminate rejects and conform to all Regulatory requirements. These processes are developed by scientists using past knowledge and 1 variable-at-a-time experiments and then subjected to process validation. Unfortunately\, more often than not\, even validated processes fail. \nAt the core of this problem is the fact that full process knowledge has not been acquired and all critical factors have not been identified. This implies that the manufacturing process can drift into a region not fully explored and produce an output that falls outside acceptable limits. \nFor the past decade and more the pharmaceutical industry\, supported by Regulators\, has been looking to Quality by Design (QbD) to remedy this problem. In pharmaceutical manufacturing the concept is to carry out experimentation and analysis using multivariate statistical techniques to determine all the factors influencing the process (critical factors)\, determining the complete region around those factors that produce a given output (design space) and then determining the optimal portion of the design space that produces the desired output within limits (optimization). \nIn this webinar participants will learn about:\n\nBasic concepts of Quality by Design (QbD)\nAdvantages of QbD over traditional 1 variable-at-a-time experimentation\nStatistical experimental design\nCritical factors\nFactor interactions\nDesign space\nInterpretation of data derived from QbD\nA real life example of QbD applied to a pharmaceutical granulation process to fully understand the critical factors and the optimal operating range within the design space for those factors\n\nNote: Course outline is subject to change without notice. Please check back regularly for updates. \nWho Should Attend\nThe webinar is suitable for those who are seeking to get a basic understanding of the concept of Quality by Design and its application to pharmaceutical processing including personnel in Production\, Quality Assurance\, Quality Control\, Validation and Development.
URL:https://www.aaps.ca/event/live-webinar-optimization-of-a-pharmaceutical-granulation-process-using-quality-by-design-qbd
LOCATION:AAPS Training Center\, 200 Consumers Road\, Suite 200\, Toronto\, Ontario\, M2J 4R4\, Canada
CATEGORIES:Live Webinars
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20200318T140000
DTEND;TZID=UTC:20200318T163000
DTSTAMP:20260430T074517
CREATED:20190730T233725Z
LAST-MODIFIED:20211208T174725Z
UID:10905-1584540000-1584549000@www.aaps.ca
SUMMARY:Review of the Safe Food for Canadians Regulations and Preventative Control Plan
DESCRIPTION:Live Webinar Review of the Safe Food for Canadians Regulations and Preventative Control Plan    \n    \n\n        \n  \n\n\n\n\n\n\n\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\nNote: Course outline is subject to change without notice. Please check back regularly for updates. \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/review-of-the-safe-food-for-canadians-regulations-and-preventative-control-plan
CATEGORIES:Live Webinars
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END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20200312
DTEND;VALUE=DATE:20200314
DTSTAMP:20260430T074517
CREATED:20190731T001018Z
LAST-MODIFIED:20211129T195203Z
UID:10921-1583971200-1584143999@www.aaps.ca
SUMMARY:Cannabis Retail Operations and Management Workshop
DESCRIPTION:Cannabis Retail Operations and Management Workshop	\n\n\n\nLive interactive and instructor led\n \n \nAbstract\nThe Cannabis Act establishes that provincial\, territorial and municipal governments will determine the framework for the retail distribution of cannabis. As a result of each province creating their own retail model\, a patchwork system has formed across Canada with different rules and regulations depending on what province and municipality you plan to operate in.  \nOpportunities to establish private cannabis retail businesses will be available in Ontario\, Alberta\, Saskatchewan\, Manitoba\, Yukon\, Nunavut\, Newfoundland and Labrador. Applications for a cannabis retail licence will be primarily handled by the liquor and gaming control boards of each province. It is important for potential retailers to properly prepare themselves in order to ensure that they will successfully obtain the required licence(s) and authorization. \nThis workshop will help guide you through the application process including the form and manner for submitting an application for a Cannabis Operator Licence and Store Authorization in Ontario and the information that is required to be submitted. A thorough overview of the Cannabis Retail Act will be provided focusing on the Registrar’s standards that have been established. This includes store and security requirements\, advertising and promotional restrictions\, required staff training\, background checks\, record keeping and documentation practices\, and maintaining compliance with the federal cannabis tracking system. \nCourse Outline\n\nCannabis Retail Regulations\, Licensing and Application Requirements\nCannabis Botany\, Product Categories and Responsible Retailing\nCannabis Retail Operations\nSupply Chain Management\, Buying and Merchandising\nStore Design and Layout\nStaff management\, training and development.\n\nThis course will deliver the tools to enable you to:\n\nApply for a Cannabis Retail Operator or Store Authorization Licence\nUnderstand best practices related to store and security requirements\nDevelop knowledge on the various cannabis products available in the Canadian market\nOwn and operate your own cannabis retail store\nUnderstand the supply chain in relation to cannabis in Ontario\nProper procedures for hiring\, training and developing staff.\n\nWho Should Attend\nCannabis industry professionals including employers and employees\, those who are interested in obtaining a cannabis retail licence\, or retail store manager licence.  \nCertificate of Attendance and Course Material\n\nAll participants will receive a certificate of attendance upon completion of the course.\nThe participants will be receiving specially prepared course manual.
URL:https://www.aaps.ca/event/cannabis-retail-operations-and-management-workshop
LOCATION:AAPS Training Center\, 200 Consumers Road\, Suite 200\, Toronto\, Ontario\, M2J 4R4\, Canada
CATEGORIES:Live Webinars
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20200310T020000
DTEND;TZID=UTC:20200310T153000
DTSTAMP:20260430T074517
CREATED:20190801T231111Z
LAST-MODIFIED:20230120T133643Z
UID:11252-1583805600-1583854200@www.aaps.ca
SUMMARY:Live Webinar Sanitation Program for Cannabis Production – Cannabis Act
DESCRIPTION:Sanitation Program for Cannabis Production	\n	\n		\n \n\n\nCourse Overview\nGood Production Practices (GPP) of the Cannabis Act mandates that Licensed Producers ensure the cleanliness of the premises and equipment. Having effective sanitation and pre-operational Inspection procedures can minimize the risk of contamination of your product\, ingredients\, processing aids\, packaging materials\, and product contact surfaces. \nIt is therefore extremely important to understand the fundamental principle of sanitation procedures and to implement and use these procedures effectively. Lack of proper and validated cleaning and sanitation program can result in costly contamination\, return of products\, and recalls. \nThis course and workshop concentrate on three important aspects of an effective sanitation program; Premise\, Equipment and Personnel. Participants are given a thorough understanding of the importance of cleaning and sanitizing procedures and their responsibilities\, and why these are important parts of their (and not cleaners`) jobs. \nCourse Outline\n\nCannabis Regulations-Review Sanitation Requirement\, Expectation and Current Guidance\nWhat is Sanitation\nSanitation Program for\n\nPremise\nEquipment\nPersonnel\n\nSanitation Procedure (SOP) for\n\nPremise\nEquipment\nPersonnel\n\nSanitation Verification\n\nWho\, When\, What\, How\n\nSanitation Checklist\nPre-Operational Inspection\nSanitation Records\nRole of QA\nTraining of Personnel\nCleaning Agents\n Pest Control\n\nNote: Course outline is subject to change without notice. Please check back regularly for updates.
URL:https://www.aaps.ca/event/live-webinar-sanitation-program-for-cannabis-production-cannabis-act
LOCATION:AAPS Training Center\, 200 Consumers Road\, Suite 200\, Toronto\, Ontario\, M2J 4R4\, Canada
CATEGORIES:Live Webinars
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20200305T130000
DTEND;TZID=UTC:20200305T150000
DTSTAMP:20260430T074517
CREATED:20190730T003705Z
LAST-MODIFIED:20240206T164839Z
UID:10846-1583413200-1583420400@www.aaps.ca
SUMMARY:Live Webinar GMP Fundamentals
DESCRIPTION:Annual GMP Masterclass 2024\n\n\n\n\nCourse Overview\nThis webinar examines the history\, rationale\, purpose\, and GMP requirements applicable to the manufacturing\, packaging and labeling\, testing\, and control of pharmaceutical products and consequence of inaction.\nGain practical knowledge in understanding of the essential elements and quality systems required for GMP and for maintaining compliance in the pharmaceutical industry. \nCourse Outline\n\n	Assuring Quality in the workplace\n	The benefits of GMP compliance\n	Management Responsibilities for GMP\n	SISPQ/principles of drug production\n	Principles of GMP\n	Training/Effective Training Requirements\n	GMP Documents\n	Standard Operating Objectives\n	Quality Control/Quality Assurance\n	Methods and Specifications\n	Sanitation Programs\n	Out of Specification and Deviation Investigations\n	Production Controls\n	Good Documentation Practice\n	Record Keeping\n	Validation and their types\n	Effective Change Control\n	Industry Trends\n	Hosting Inspectors and Auditors\n\nWHO SHOULD ATTEND\nThis course is valuable for Directors\, Managers\, Supervisors\, Associates in the Pharmaceutical\, Biopharmaceutical\, Vitamins\, Herbals\, Medical Devices and allied industries with daily responsibilities in the following areas: \n\n	Regulatory Affairs\n	Clinical Research\n	Quality Assurance\n	Documentation and Technical Writing\n	Product Submission\n	Project Management\n	Training\n	Product Development\n	Consultants\n	Others who interact together to launch a product
URL:https://www.aaps.ca/event/live-webinar-gmp-fundamentals
LOCATION:AAPS Training Center\, 200 Consumers Road\, Suite 200\, Toronto\, Ontario\, M2J 4R4\, Canada
CATEGORIES:Live Webinars
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20200304T130000
DTEND;TZID=UTC:20200304T150000
DTSTAMP:20260430T074517
CREATED:20190801T232117Z
LAST-MODIFIED:20230119T203651Z
UID:11255-1583326800-1583334000@www.aaps.ca
SUMMARY:Live Webinar How to Write Effective Standard Operating Procedures (SOPs)
DESCRIPTION:SOP Must Haves	\n	\n	\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/live-webinar-how-to-write-effective-standard-operating-procedures-sops
LOCATION:AAPS Training Center\, 200 Consumers Road\, Suite 200\, Toronto\, Ontario\, M2J 4R4\, Canada
CATEGORIES:Live Webinars
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20200227T140000
DTEND;TZID=UTC:20200227T153000
DTSTAMP:20260430T074517
CREATED:20190730T011001Z
LAST-MODIFIED:20210423T171852Z
UID:10851-1582812000-1582817400@www.aaps.ca
SUMMARY:Cannabis Micro License Requirements and Application Webinar
DESCRIPTION:Live Webinar Cannabis Micro Licence Application Process and Requirements\n\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\n	Background\n	Cannabis Micro Licence classes and subclasses\n	Cannabis Tracking and Licensing System (CTLS)\n	Application process and steps\n	Application documentation requirements\n	Key positions\, site personnel and security clearances\n	Site security plan\n	Organizational security plan\n	Site & building information\n	Good Production Practices (GPP) plan\n	Record keeping and reporting methods\n	QA person\, master grower\, head of security\, head of client services\, SPIC\, RPIC\n	Notices to the local authorities\n	Approval process\n	Refusal and withdrawals\n	Changes to the application\n	Current licences transitions – Equivalent licences under the Cannabis Act\n	Application 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/live-webinar-cannabis-micro-licence-application-process-and-requirements
LOCATION:AAPS Training Center\, 200 Consumers Road\, Suite 200\, Toronto\, Ontario\, M2J 4R4\, Canada
CATEGORIES:Live Webinars
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20200115T140000
DTEND;TZID=UTC:20200115T160000
DTSTAMP:20260430T074517
CREATED:20190801T195751Z
LAST-MODIFIED:20200408T004240Z
UID:11143-1579096800-1579104000@www.aaps.ca
SUMMARY:Live Webinar GMP and GACP for the Cannabis Industry
DESCRIPTION:Live Webinar GMP and GACP for the Cannabis Industry	\n	\n		\n	Register online \n \n\nDates Available\nJanuary 15 \, 2020 \nTime\n2:00 p.m – 4:00 p.m. \nCost\nCAD $385.00 + HST \nLocation\nOnline Webinar\n\n\n\n\n\n \n\n\nAbstract\nCurrently\, there are no GMP requirements for cannabis products\, it’s almost certain that in the future\, cannabis regulations will require GMP certification for Licensed Producers (LPs) to receive and maintain their license. Even now\, sales opportunities may be lost by not maintaining GMP certification as exporting cannabis for medicinal purposes to Europe requires GMP compliance. As a result\, more and more consumers will expect to see the certification on the product they buy. For business to business cannabis sales\, many LPs are already requiring GMP certification from any other LPs they buy product from. \nGood Manufacturing Practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any production that cannot be eliminated through testing the final product. \nGMP covers all aspects of production from the starting materials\, premises and equipment to the training and personal hygiene of staff. Detailed\, written procedures are essential for each process that could affect the quality of the finished product. There must be systems to provide documented proof that correct procedures are consistently followed at each step in the manufacturing process – every time a product is made. \nIn Europe\, European Medicinal Agency (EMEA) requires adherence to Good Agricultural and collection Practices (GACP) for growing and harvesting of herbal medicine. Both GACP and GMP are designed to ensure full traceability back to the seed source for each crop. Following GACP and GMP standards ensures that only the highest quality plants are grown and harvested. \nCourse Outline\nGMP \n\nWhat is GMP\nWhen GMP is needed\nEssential Elements of GMP\n\nPeople and Product\nPremises and Equipment\nDocumentation and Standard Operating Procedures (SOPs)\nNon-Conformances/Deviations\, Recalls & Complaints Handling\nValidation\nChange Management\n\n\nEMEA – GACP \n\nQA\nPersonnel and Education\nBuildings and Facilities\nEquipment\nDocumentation\nSeeds and Propagation material\nCultivation\nCollection\nHarvest\nProcessing\nPackaging\nStorage and Distribution\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\, consultants\, and suppliers to the industry.
URL:https://www.aaps.ca/event/live-webinar-gmp-and-gacp-for-cannabis-industry
LOCATION:AAPS Training Center\, 200 Consumers Road\, Suite 200\, Toronto\, Ontario\, M2J 4R4\, Canada
CATEGORIES:Live Webinars
ATTACH;FMTTYPE=image/jpeg:https://www.aaps.ca/wp-content/uploads/1920x560-Desktop-Live-Webinar.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20191203T140000
DTEND;TZID=UTC:20191203T160000
DTSTAMP:20260430T074517
CREATED:20190730T010552Z
LAST-MODIFIED:20210423T170128Z
UID:10849-1575381600-1575388800@www.aaps.ca
SUMMARY:Live Webinar Good Production Practices (GPP) and Good Agricultural and Collection Practices (GACP) for the Cannabis Industry – Canada & Europe
DESCRIPTION:Live Webinar Good Production Practices (GPP) and Good Agricultural and\n        Collection Practices (GACP) for the Cannabis Industry – Canada &\n        Europe\n      \n\n     \n      \n        \n       \n\n\n        \n     \n      Description\n      \n        In order to ensure appropriate and consistent quality of\n        medicinal/herbal substances\, it is necessary to establish good practices\n        in growing\, harvesting\, and processing operations. Cannabis Act requires\n        Licensed Producers to implement and adhere to Good Production Practices\n        (GPP). In Europe\, European Medicinal Agency (EMEA) requires adherence to\n        Good Agricultural and collection Practices (GACP) for growing and\n        harvesting. Both GACP and GPP are designed to ensure full traceability\n        back to the seed source for each crop. Following GACP and GPP standards\n        ensures that only the highest quality plants are grown and harvested.\n       \n      Outline\n      Cannabis Act – GPP \n      \n        \n          Analytical Tests\, Microbial and chemical contaminants and pest control\n          products\n        \n        Premises\n        Equipment\n        Sanitation Program – Premise\, Equipment\, Personnel\n        Standard Operating Procedures\n        Recall and Recall Reporting\n        Quality Assurance\n        Retained Samples\n        Adverse Reactions and Adverse Reactions Reporting\n      \n      EMEA – GACP \n      QA\n      Personnel and Education\n      Buildings and Facilities\n      Equipment\n      Documentation\n      Seeds and Propagation material\n      Cultivation\n      Collection\n      Harvest\n      Processing\n      Packaging\n      Storage and Distribution\n\n      \n        \n        Note: Course outline is subject to change without notice. Please\n        check back regularly for updates.
URL:https://www.aaps.ca/event/live-webinar-good-production-practices-gpp-and-good-agricultural-and-collection-practices-gacp-for-the-cannabis-industry-canada-europe
LOCATION:AAPS Training Center\, 200 Consumers Road\, Suite 200\, Toronto\, Ontario\, M2J 4R4\, Canada
CATEGORIES:Live Webinars
ATTACH;FMTTYPE=image/jpeg:https://www.aaps.ca/wp-content/uploads/1920x560-Desktop-Live-Webinar.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20190821T130000
DTEND;TZID=UTC:20190821T150000
DTSTAMP:20260430T074517
CREATED:20190730T234818Z
LAST-MODIFIED:20200402T224037Z
UID:10911-1566392400-1566399600@www.aaps.ca
SUMMARY:Live Webinar Writing GPP and Quality Assurance Report for Health Canada
DESCRIPTION:Live Webinar Writing GPP and Quality Assurance Report for Health Canada	\n	\n		\n	Register online \n \n\n\nDates Available\nMay 6\, 2020 \nTime\n1:00 p.m – 3:00 p.m. \nCost\nCAD $385.00 + HST \nLocation\nOnline Webinar \n \nAbstract:\nHealth Canada requires all Licence Producer Applicant to submit a written and approved GPP (Quality Assurance) Report at the time of the application submission. This GPP report provides the main framework for establishing the organization’s Quality Assurance Systems.  \nEffective and comprehensive GPP report allows a smooth journey through out the licensing process and forms a basis for consistently meeting the quality and compliance requirements established by Health Canada.  \nThis webinar is designed to provide helpful information and essential training towards writing an effective GPP report acceptable to Health Canada’s Cannabis Licensing Department.  \nCourse Outline\n\nWhat is a GPP report?\nWho should write and sign off on GPP reports?\nGPP sections\nWriting Tips\nRoles and Responsibilities\nProduct flow chart\nPeople flow chart\n\nNote: Course outline is subject to change without notice. Please check back regularly for updates.
URL:https://www.aaps.ca/event/live-webinar-writing-gpp-and-quality-assurance-report-for-health-canada
CATEGORIES:Live Webinars
ATTACH;FMTTYPE=image/jpeg:https://www.aaps.ca/wp-content/uploads/img-featured-default.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20190814T130000
DTEND;TZID=UTC:20190814T153000
DTSTAMP:20260430T074517
CREATED:20190730T234410Z
LAST-MODIFIED:20210426T154958Z
UID:10907-1565787600-1565796600@www.aaps.ca
SUMMARY:Live Webinar Cannabis Tissue Culture
DESCRIPTION:Live Webinar Cannabis Tissue Culture	\n	\n		\n	\n\n\n\n\n\n\nDistinguished Faculty\nKimberly Belfry\n   \nKimberly Belfry holds a bachelors in biochemistry and biotechnology from the University of Saskatchewan\, a doctorate in plant science from the University of Alberta\, and is a Professional Agrologist with the Ontario Institute of Agrologists. Kimberly has published 18 peer-reviewed articles that focus primarily on weed control in commercial corn and soybean production in Ontario. In 2018\, Kimberly took on the role of Director of Cultivation for a licenced producer applicant in Ontario. Kimberly has been active in the research and design of the facility with a particular focus on tissue culture. As part of her training\, Kimberly has completed the Indoor Cannabis Horticulture Program in Oakland California.\n \nAbstract\nPlant tissue culture is a group of methods in which plant fragments\, seeds\, or individual cells may be used to propagate genetically identical offspring. Although not new to the plant sciences\, tissue culture has been rapidly gaining popularity in the cannabis sector due to its ability to produce large numbers of identical plants under sterile laboratory conditions.  \nThe cannabis industry is bringing in a lot of career opportunities to the Canadian market and is quickly becoming one of the fastest growing sectors in Canada. The rapid growth of tissue culture in the cannabis industry means there is a need for knowledgeable individuals to work in the managerial and technical roles. This workshop will give attendees a comprehensive look into tissue culture and its applications in cannabis production. Topics will include: \n\nIntroduction to tissue culture in plants\nTechniques in tissue culture\nDesigning a tissue culture lab that suits your goals and budget\n\nCourse Outline\n\nHistory of tissue culture\nPlant biology overview and introduction to totipotency\nBenefits of tissue culture in cannabis production\nMedia composition and various formulations\nPracticing good aseptic technique\nIdentifying and eliminating sources of contamination in your lab\nLaboratory design – From small to large scale\nHow to conduct your own tissue culture experiments\n\nWho Should Attend\nThis webinar is intended for those who are interested in tissue culture in cannabis; as a technician\, manager or organization looking to become a Licensed Producer (LP). No previous laboratory experience is required.
URL:https://www.aaps.ca/event/live-webinar-cannabis-tissue-culture
LOCATION:AAPS Training Center\, 200 Consumers Road\, Suite 200\, Toronto\, Ontario\, M2J 4R4\, Canada
CATEGORIES:Live Webinars
ATTACH;FMTTYPE=image/jpeg:https://www.aaps.ca/wp-content/uploads/1920x560-Desktop-Live-Webinar.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20190808T130000
DTEND;TZID=UTC:20190808T150000
DTSTAMP:20260430T074517
CREATED:20190730T011228Z
LAST-MODIFIED:20230120T132529Z
UID:10853-1565269200-1565276400@www.aaps.ca
SUMMARY:Cannabis Retail Application Process and Requirements
DESCRIPTION:Cannabis Retail Application Process and Requirements	\n	\n        \n\n\nAbstract\nThe Cannabis Act establishes that provincial\, territorial and municipal governments will determine the framework for the retail distribution of cannabis. As a result of each province determining their own retail model\, a patchwork system has formed across Canada with different rules and regulations depending on what province and municipality you plan to operate in. Opportunities to establish private cannabis retail businesses will be available in Ontario\, Alberta\, Saskatchewan\, Manitoba\, Yukon\, Nunavut\, Newfoundland and Labrador. Applications for a Cannabis Retail Licence will be primarily handled by the liquor and gaming control boards of each province.  \nAlthough the application process in each province will be slightly different in terms of store\, security\, reporting and application requirements\, best practices and what to expect when submitting an application can still be deduced. Even without full clarity on what regulations will look like in Ontario\, many potential retailers are already trying to prepare themselves to ensure that they will successfully obtain the required licence(s) and authorization. \nThis webinar discusses the application process including the form and manner for submitting an application for a Cannabis Retail Licence in Ontario and the information that is required to be submitted. \nWebinar Outline\n\nCannabis Retail Landscape Across the Provinces\nBackground\n\nCannabis Licence Act\nOCS/OCRC\nAlcohol and Gaming Commission of Ontario\n\nCannabis Tracking and Licensing System (CTLS)\nPerson Interested In (Shareholders\, Directors\, Officers\, Control\, Financing)\nRetail Operator Licence\n\nEligibility\nRestrictions\nScope\nIssuance\nRefusal\n\nRetail Store Authorization\n\nMunicipal Zoning Restrictions\, Opt In/Out\nStore Restrictions\nLP Restrictions\nEligibility\nRefusal\nPublic Notice\nIssuance\n\nRetail Manager Licence\n\nFunctions and Responsibilities\nEligibility\nRefusal\n\nAdditional Conditions\n\nOngoing Sale\nUse of Seal\nMinimum Pricing\nRenewals\n\nOperational Restrictions\n\nSourcing Product\nSelling to Minors\nSelling to Intoxicated Persons\nPurchase Limits\nRecorded Sales\nOnline Sales\nUnsold Cannabis\nDiversion\n\nEnforcement\n\nRevocations and Suspensions\nHearings\nInquiries and Investigations\n\nLeasing and Rental Agreements\n\nSite & building information\nOntario Building Code\nRent Negotiations (Security Deposits\, Commencement Date\, Licence Issuance)\nThird Parties (Existing Lenders\, Existing Tenants\, Mortgages\, Insurance\, Non-disturbance)\nEnhanced provisions\n\nSecurity Requirements\n\nPhysical Access (Perimeter)\nAlarm System\nCCTV\nPanic Button\nEmployee Safety\n\nStore Requirements\n\nPoint-of-Sale System\nReceiving Area\nCustomer Area\nStorage Area\nProduct Displays\n\nFinancial Disclosure\nBusiness Plans\nProduct Promotions\n\nSignage\, Branding and Advertising\nProhibited Promotion (Lifestyle\, Price and Availability\, Testimonial\, Lifestyle/Emotion\, False or Misleading)\nEducational/Informational Promotion and Marketing\nBrand-Preference\nSales Representatives\n\n\nNote: Course outline is subject to change without notice. Please check back regularly for updates. \nWho Should Attend\nCannabis industry professionals including employers and employees\, those who are interested in obtaining a cannabis retail licence\, working in a cannabis retail store or pro.
URL:https://www.aaps.ca/event/cannabis-retail-application-process-and-requirements
LOCATION:AAPS Training Center\, 200 Consumers Road\, Suite 200\, Toronto\, Ontario\, M2J 4R4\, Canada
CATEGORIES:Live Webinars
ATTACH;FMTTYPE=image/jpeg:https://www.aaps.ca/wp-content/uploads/1920x560-Desktop-Live-Webinar.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20190726T023000
DTEND;TZID=UTC:20190726T153000
DTSTAMP:20260430T074517
CREATED:20190730T180937Z
LAST-MODIFIED:20200407T234707Z
UID:10870-1564108200-1564155000@www.aaps.ca
SUMMARY:Pharmaceutical Quality Assurance and Quality Control
DESCRIPTION:Dates Available\n	July 26\, 2019 \n	Time\n	2:30 p.m. – 3:30 p.m. \n	Technical Requirement\n	Internet and Phone Connection or Internet and VoIP Connection \n	Webinar Outline\n	\n		\n			\n				\n					\n						Pharmaceutical Industry\n						Quality Assurance and Quality Control Careers\n						Salary Expectations\n						Qualifications required\n						AAPS Difference\n					\n				\n				\n					\n						Training and Professional development programs\n						Financial Aid\n						How to Register\n						Q&A
URL:https://www.aaps.ca/event/pharmaceutical-quality-assurance-and-quality-control
LOCATION:AAPS Training Center\, 200 Consumers Road\, Suite 200\, Toronto\, Ontario\, M2J 4R4\, Canada
CATEGORIES:Live Webinars
END:VEVENT
END:VCALENDAR