Newsletter

QT ANALYSIS: OVERVIEW OF NEW AND IMPACTING GLOBAL REGULATORY UPDATE FOR 2024  - DECEMBER/JANUARY 2024

QT ANALYSIS: OVERVIEW OF NEW AND IMPACTING GLOBAL REGULATORY UPDATE FOR 2024 - DECEMBER/JANUARY 2024

  • 2023-12-28 09:01:53

In this latest edition, we navigate the evolving landscape of medical device regulations, marked by progress and heightened vigilance. The improvement of technology and healthcare is making things better for patients, but it also needs careful supervision. Over the past year, global regulatory bodies have demonstrated adaptability, reinforcing frameworks to manage medical device registrations effectively.

This edition offers a concise analysis of the latest mandates, impending updates, and pivotal shifts for 2024, addressing the exchange between technological innovation and the mission to ensure global safety and efficacy.

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QT ACTIVITY: QUALTECH DRIVES GROWTH IN THE ASEAN REGION THROUGH TRANSFORMATIVE BUSINESS DEVELOPMENT MEETING  - DECEMBER/JANUARY 2024

QT ACTIVITY: QUALTECH DRIVES GROWTH IN THE ASEAN REGION THROUGH TRANSFORMATIVE BUSINESS DEVELOPMENT MEETING - DECEMBER/JANUARY 2024

  • 2023-12-26 05:15:49

Qualtech's regional meeting united leaders from across ASEAN to collaborate, share knowledge, and shape the future of Qualtech in the region. The event focused on fostering unity, unwavering commitment to quality with ISO 13485 standards, and strategic planning for each country's unique needs. A cultural immersion tour of Chulalongkorn University provided inspiration and deeper understanding. The meeting concluded with a shared vision for the future of Qualtech in ASEAN.

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SINGAPORE: CYBERSECURITY LABELLING SCHEME FOR MEDICAL DEVICES SANDBOX - DECEMBER/JANUARY 2024

SINGAPORE: CYBERSECURITY LABELLING SCHEME FOR MEDICAL DEVICES SANDBOX - DECEMBER/JANUARY 2024

  • 2023-12-26 02:27:39

Following the industrial consultation earlier this year, Cyber Security Agency (CSA) of Singapore is launching Sandbox as a voluntary trial program for Cybersecurity Labelling Scheme for Medical Devices (CLS(MD)). This program started on 20th October 2023 and will be held for 9 months. CSA is inviting medical device manufacturers to participate in Sandbox to have a first-mover advantage in enhancing the security of their products.

The Sandbox allows all parties involved to test out and give feedback on the requirements and application process for the CLS(MD) ahead of the scheme’s launch. Along with the launch of Sandbox program, CSA also published intensive set of regulations related to the requirements and implementation of CLS(MD).

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QT ACTIVITY: KOREA MARKET EXPANSION AND CHINA NMPA UPDATES WEBINAR SUMMARY - NOVEMBER/DECEMBER 2023

QT ACTIVITY: KOREA MARKET EXPANSION AND CHINA NMPA UPDATES WEBINAR SUMMARY - NOVEMBER/DECEMBER 2023

  • 2023-11-20 03:05:02

On October 20, Qualtech hosted a webinar titled "Korea Market Expansion and China NMPA Updates." With over 60 global participants, the event marked Qualtech's entry into the Korean market, sharing actionable steps for successful medical device registration. The second segment covered key changes in China's Medical Device regulations from September 2022 to August, ensuring attendees were informed about the latest regulatory developments.

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