Presented by CA Member Dell Tech Laboratories Ltd. and the medical device trade association Medtech Canada.
Date: Wednesday, November 27, 2024
Time: 10:00 am – 12:00 pm EST
Cost: Member: $250, Non Member: $395
This session is open to members and non-members of Cosmetics Alliance and is composed of two parts:
Part I – Presented by DellTech
- Learn the classification landscape of devices used in the cosmetics industry
Part 2 – Presented by MedTech Canada
- Understand which Acts & Regulations apply when your device is a Medical Device.
- Learn the most recent and updated regulations and requirements for Medical Device
Intended For:
- Compliance specialists
- Anyone interested in learning the objectives
This session includes exercises, a quiz, and a Q&A session.
Training certificates are provided to everyone who successfully completes the quiz, for their records.
Individual logins are required for each participant to obtain a training certificate.
About the Trainers
Mia Spiegelman, VP Regulatory Affairs, Medtech Canada
Mia Spiegelman is the Vice President Regulatory Affairs at Medtech Canada and holds a B.Sc. in Chemistry from York University as well as Certification in Pharmaceutical Regulatory Affairs and Quality Operations from Seneca College. Throughout her 24 years in industry, she has worked in various Medical Device, Pharmaceutical, Cosmetic and Consulting companies while holding various roles within the Quality and Regulatory fields. Her current role responsibilities include developing, leading, implementing and managing the Regulatory, Quality and Environmental strategic initiatives for Medtech Canada and its members in order to ensure that Canada has a globally competitive regulatory environment.
Ivy Tang, Principal Regulatory Consultant, Dell Tech Laboratories
Ivy is a seasoned regulatory consultant with over 9 years of experience specializing in chemical hazard communication, client relations, and regulatory compliance. Her expertise covers SDS authoring, consumer packaging and labelling, CFIA premarket assessments, HMIRA submissions, cosmetic notifications, VOC, and transportation consulting. Ivy also has extensive experience in managing consumer product recalls and guiding businesses through complex regulatory landscapes.
Since 2020, Ivy has worked closely with Canadian vaping industry stakeholders, developing training programs and ensuring compliance with Vaping Products Labelling and Packaging Regulations. In her current role, she is excited to expand her focus to medical device licensing and quality assurance, helping businesses meet rigorous regulatory standards and achieve market success.
Stephen McCarthy, Director of Regulatory Affairs, Dell Tech Laboratories
Steve joined Dell Tech, as a Director of Medical Device & Quality Assurance with over 25 years of experience in the healthcare and regulated therapeutics products industry. Prior to joining Dell Tech, he lead a consulting group with a global reputation for best-in-class services to the cosmetics, drugs, foods, medical devices, and natural health products industries. Before entering consulting, he worked for 15 years in sales and marketing roles for therapeutic products and prior to that he delivered front-line cardiac rehabilitation healthcare services. With his deep understanding of the quality assurance and regulatory requirements for Canada he works with clients to strategize the optimal path to meet milestones, bring products to market, and manage them through their lifecycle. Steve has a track record of creating effective and very long-standing partnerships that creates value for clients and their brands in Canada.
Steve serves on the Executive Committee and Board of Directors of Cosmetics Alliance Canada.
