Webinar Center

This webinar introduces the European Union Medical Device Regulation (EU MDR) and its implications for medical device manufacturers seeking access to the European market. Participants will explore the regulation’s key requirements, medical device classification, conformity assessment, CE marking, and post-market surveillance obligations.

Join our experts to understand the latest changes to China’s GB 6675 toy safety standards and what they mean for testing, China Compulsory Certification (CCC) and market access.

SGS webinar to gain practical understanding of supply chain due diligence, its business value, and the increasing regulatory and customer expectations for responsible supply chains.

This webinar provides an overview of ISO 13485:2016 and its role in establishing an effective quality management system for organizations involved in the medical device industry. Participants will explore the standard’s key requirements, risk management principles, and relevant regulatory considerations throughout the medical device life cycle.

Join our webinar to explore the key changes introduced by EN 16781:2026 for children's sleep bags and other developments affecting textile childcare safety.

Join our complimentary webinar to gain a better understanding of FDA import alerts affecting shrimp and seafood supply chains.

ISO 9001 est la norme de management de la qualite la plus largement adoptee au monde et les etablissements denseignement superieur y recourent de plus en

This webinar introduces the key concepts and requirements of IATF 16949:2016 and highlights its importance in the automotive industry and automotive supply chain. Participants will explore automotive-specific quality management requirements, the process approach, risk-based thinking, and the role of core tools in supporting product quality and continual improvement.