Medical Device Regulation (MDR) Post Market Surveillance Requirements

Day 1: Overview of the EU MDRJoin us for a comprehensive one-day training course providing an in-depth overview of the European Medical Device Regulation (EU MDR). Designed to equip medical device professionals with essential knowledge, this course covers key aspects of the EU MDR, including regulatory requirements, compliance strategies, and implementation challenges. Through engaging presentations, case studies, and discussions, participants will gain insights into the changes introduced by the EU MDR and learn how to navigate the regulatory landscape effectively.Day 2: MDR Risk Management: Pre and Post MarketThis dynamic one-day training course focuses on mastering risk management under the MDR, covering both pre- and post-market risk assessment strategies. Special emphasis is placed on software, artificial intelligence (AI), and cybersecurity considerations. Participants will learn key concepts, methodologies, and tools for identifying, evaluating, and mitigating risks throughout the device lifecycle. Through interactive sessions and practical exercises, attendees will gain insights into ensuring compliance with MDR requirements while optimizing product safety and effectiveness.Day 3: MDR Clinical EvaluationThis intensive one-day training course provides comprehensive knowledge and skills for navigating clinical evaluation under the MDR. The program covers essential concepts, methodologies, and regulatory requirements for clinical investigation and post-market surveillance. Through interactive lectures, case studies, and exercises, attendees will learn how to conduct robust clinical evaluations, ensure compliance with MDR guidelines, and optimize post-market surveillance strategies. This course is ideal for those involved in product development, regulatory affairs, clinical research, or quality management.Day 4: MDR Documentation RequirementsThis comprehensive one-day training course focuses on the essential documentation requirements mandated by the MDR to ensure regulatory compliance and facilitate market access for medical devices. Participants will learn how to create, manage, and maintain documentation that adheres to MDR standards. The course covers the full spectrum of required documentation, including technical documentation, clinical evaluation reports, and post-market surveillance plans. Through interactive sessions and practical exercises, attendees will gain the knowledge and tools to navigate MDR documentation requirements confidently.Day 5: MDR Post Market Surveillance Requirements This one-day training course provides in-depth insights into the post-market surveillance (PMS) requirements outlined in Annex III of the MDR. Participants will learn how to establish a robust PMS system, conduct trend analysis, and implement corrective actions. Through interactive discussions and case studies, attendees will explore key concepts and best practices for managing post-market surveillance activities. This course equips participants with practical skills and strategies to enhance product safety and performance while meeting regulatory obligations."

SGS is excited to bring to the GTA a comprehensive full-day symposium focused on the medical device industry. In partnership with the RAPS Ontario Chapter, the leading association for regulatory professionals, we will focus on navigating the latest quality and regulatory challenges in the Medtech industry, including AI in Medical Device, the latest developments in MDR, a guide to MDSAP and more. Join us for this exciting conference.Key Highlights:Sessions on Medtech Design, AI, MDSAP, and MDSAP, and MDR/IVDR ComplianceValuable networking opportunities and full-day programming (including lunch!)20% off for future training