Ensuring Quality and Cyber Resilience: Medical Devices’ Ecosystem & Singapore Standards in Medical Device Compliance

Ensuring Quality and Cyber Resilience: Medical Devices’ Ecosystem & Singapore Standards in Medical Device Compliance

 

This seminar brings together industry experts, standard development organizations, and regulatory practitioners to explore key quality management and cybersecurity requirements shaping the medical device sector. Participants will gain clarity on the Singapore Accreditation Council (SAC) ISO 13485 and the latest Singapore Standards, as well as Medical Device life cycle and supply chain management to improve compliance with Health Science Authority (HSA) and US FDA regulations and enhance market access. The program features panel discussions that address the nuanced differences between various variations of Medical Device Quality Systems, providing practical guidance for medical device manufacturers and suppliers operating in Singapore. Additionally, attendees will be introduced to Singapore’s cybersecurity standards through an interactive workshop, followed by a panel discussion on the roadmap and guiding principles for strengthening cybersecurity in the MedTech industry. The event aims to equip professionals with both strategic understanding and actionable insights to ensure compliance, quality, and resilience in a rapidly evolving regulatory landscape. 

This is a free for member event.

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