FREE Webinar for CAPRA Members
Regulatory and Quality updates impacting Medical Devices
Regulatory and Quality updates impacting Medical Devices
Mia Spiegelman will provide an update on few key areas critical to the medical device industry such as the MDSAP Program, Current Environmental Regulations impacting Medical Devices as well as Regulatory Updates and initiatives that Medtech Canada is working on.
Dr. Sherry Boodram
CEO & Co-founder, CannDelta Inc
ABOUT OUR GUEST
Dr. Sherry Boodram is the CEO and Co-Founder of CannDelta Inc., a top regulatory and scientific cannabis consulting firm specializing in licensing and compliance across the US, Canada, and international markets. With extensive experience in cannabis regulations, Dr. Boodram has a unique background, including working within the Health Canada’s Cannabis and Controlled Substances Programs. She has overseen cannabis and controlled substances inspections and reviewed associated licensing applications, offering deep insights into regulatory compliance, licensing, and quality management systems within these regulated industries.
At CannDelta, Dr. Boodram has helped launch over 400 cannabis businesses, has supported governments in developing cannabis regulations and policies, and continues to provide strategic guidance to various firms including those aiming to expand internationally. She sits on various boards and holds a Ph.D. in Chemistry from York University and additional qualifications in Cannabis Law, Pharmaceutical Regulatory Affairs, and Quality Operations.
Tuesday, July 29, 2025
Online
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Presentation with Guest Speakers
1:00 pm - 2:00 pm EDT