Having an effective PMS system is important from both a regulatory and quality perspective. This webinar will help manufacturers to learn about the key requirements, concepts and the overall process for post-market surveillance under the MDR. Based on regulatory requirements and operational tools provided during the webinar, you will be able to write your PMS documentation that includes both proactive and reactive sources of information.
The Post Market Surveillance: Regulatory requirements and practical implications
FREE ONLINE WEBINAR: To continue supporting our customers' needs this webinar is dedicated to manufacturers only. To allow all interested companies attend, maximum two delegates form the same company will be admitted. Due to the type of event and limited audience capacity, participation of companies not included in this category will not be accepted. Attendance will be confirmed from the event's organizers.
DATE: March 14, 2024 | 3.00 PM - 4.00 PM CET
OFFICIAL LANGUAGE: English
SUBMISSION LINK: https://attendee.gotowebinar.com/register/1489606695293957468
ATTENDEES CAPACITY: 500 delegates
The event will be hosted within Go ToWebinar platform. Your registration request for this webinar will be submitted to the organizer for approval. You will receive information via email regarding your registration status.
Speakers
Daniele Lioi is a Senior Consultant and Team Manager of the Eurofins Italian Medical device consultancy team. Since 2017, he has been dealing with Biological Risk assessments, Clinical Evaluation and Supporting the compilation of the technical documentation for medical device manufacturers. He has a biotechnology background with experience in regulatory affairs of medical devices. Daniele recently obtained the qualification as Auditor/Lead Auditor ISO 13485/ISO 9001, he is included in the national registry for person responsible for regulatory compliance and he joined the HAS consultants team for the harmonization of International Standards.
Mariarosaria Sollo is a Senior medical device consultant and a Lead Auditor for Eurofins Regulatory & Consultancy Services Italy