ISO 13485:2016 – Introduction and implementation
We recommend this seminar if you would like to familiarize yourself with the contents of ISO 13485:2016 and options for its practical implementation. The medical devices standard ISO 13485:2016 has been issued. What are the key changes compared to ISO 13485:2012? What are the requirements for the quality management systems of medical device manufacturers? At the heart of ISO 13485:2016 is a comprehensive process risk management to be integrated in all medical device-related quality management processes of the company, including outsourced supplier processes. In addition to development and production, this includes processes that take place after the medical devices are placed on the market. Our two-day seminar will provide you with basic knowledge regarding ISO 13485:2016 and, as part of an implementation workshop, will explain in detail how to integrate the requirements for quality management systems in your company processes.
- Introduction to the legal and regulatory environment of ISO 13485:2016
- Legal environment (national and international) and regulatory framework
- Lifecycle of a medical device
- Classification of ISO 13485:2016
- ISO 13485:2016 in detail
- Process validation and risk analysis, documentation
- Qualification and infrastructure
- Development (design control, clinical data, validation)
- Vendor management
- Production management
- Continuous improvement process (CIP): internal errors, complaints, risks
- Corrective actions, preventive measures
- Corrective and Preventive Actions (CAPA), reporting process
- Deepening of the standard section in a practical workshop
As a participant, you will receive a copy of the standards book „Quality Management and Risk Management for Medical Devices ISO 14971 and ISO 13485“.
- Medical device manufacturer and vendor personnel who will be involved in the launch of management systems or updating of the current management system
- Quality management officers (QMOs), product managers, Regulatory Affairs personnel
- Consultants in the medical device industry
As a participant, you will receive a copy of the standards book „Quality Management and Risk Management for Medical Devices ISO 14971 and ISO 13485“.
English
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Dieses Onlinetraining wird von der TÜV SÜD Akademie GmbHin Deutschland durchgeführt. Bei diesem Onlinetraining gelten daher die AllgemeinenGeschäftsbedingungen und Prüfungsordnungen sowie Datenschutzinformationen der TÜV SÜD Akademie GmbH. Bei Rückfragen stehenwir Ihnen gerne zur Verfügung.
This training is being operated by TÜV SÜD Akademie GmbHin Germany. The GeneralTerms and Conditions as well as the PrivacyNotice of TÜV SÜD Akademie GmbH apply. Incase of any questions, do not hesitate to contact us.