Live Webinar Cannabis Industry Complaints and Recalls
July 13, 2018
2:00 p.m – 4:00 p.m.
CAD $345.00 + HST
AAPS Training Center
200 Consumers Road, Suite 200, Toronto, Ontario, M2J 4R4
Mr. Steven Tanner has worked for and partnered (GQRP) with the top global pharmaceutical manufacturing, contract research, wholesale and specialty distribution organizations in both Europe and North America. From Eli Lilly UK to Merck KGaA (now Mylan) in Canada, Pharmanet (now Inventiv Health), Teva, and the McKesson Corporation, Steven now surpasses more than 18-years of progressive GxP industry experience in quality, compliance and technical training senior leadership roles.
Steven’s specialties include leading FDA and Health Canada GMP inspections, customer 3rd party logistics (3PL) quality & qualification audits, as well as the hands-on design, strategy, execution and management of GxP regulatory quality systems: change controls, deviation controls, CAPA, validation/21 CFR Part 11, document controls, environmental monitoring, complaints, equipment & shipment qualifications, SOPs, technical writing, drug recalls, quality agreements, self-inspections. Steven has also partnered since 2004 with AAPS – Academy of Applied Pharmaceutical Sciences where he’s provided quality assurance/GxP technical facilitation. In 2016 Steven accepted a full-time role as Campus Manager and Director of Student Affairs with AAPS.
Steven graduated in 1999 with an honours degree in Chemistry from Leicester University in the United Kingdom and holds a postgraduate diploma in Adult Education from St Francis Xavier University, Nova Scotia, Canada.
This webinar examines the application of ACMPR – Access to Cannabis for Medical Purposes Regulations GPP Good Production Practice requirements applicable to Product Recalls and Complaints for the cannabis industry and consequences of inaction.
Gain practical knowledge in understanding of the essential elements for maintaining compliance in the cannabis industry.
- Recall and Recall Reporting per ACMPR GPP regulatory requirements
- Standard Operating Procedure requirements
- Quality Assurance roles/responsibilities
- Adverse Reactions and Adverse Reactions Reporting
- Consequences/case studies
Note: Course outline is subject to change without notice. Please check back regularly for updates.
Who Should Attend
This course is valuable for Directors, Managers, Supervisors and Associates in the medical cannabis industry with daily responsibilities in the following areas:
- Regulatory Affairs
- Quality Assurance
- Documentation and Technical Writing
- Project Management
- Product Development