• 2024-04-08 08:22:03

This article explores Qualtech's strategy to achieve this feat, including navigating China's complex regulatory framework and leveraging an experienced medical writing team. The outcome is a faster market entry for Qualtech's product, offering a significant advantage in the lucrative Chinese market.

• 2024-01-26 07:26:23

Reflecting on 2023, Qualtech experienced a dynamic and transformative year marked by regulatory webinars and the establishment of a new office in Korea. Amid challenges and celebrations, we fortified our commitment to excellence, setting the stage for continued growth and even greater achievements in the future. Join us in revisiting the highlights that shaped our journey.

• 2024-01-04 02:44:21

Join us on our upcoming webinar and don't miss this chance to get expert EU MDR insights in the registration of aesthetic-purpose devices. See you on January 25, 2024 at 5 PM Taipei Time (10 AM CET)!

• 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.

• 2023-07-24 10:42:16

恭喜首位Qualtech博士課程實習生完成學位，順利博士畢業!

• 2023-09-28 06:42:53

理工科技誠摯邀請您參加將於2023年10月20日(星期五)舉行的網路研討會。

• 2023-07-21 03:58:08

Qualtech hosted a talk by Dr. Huang Wen-Chien on the evolution of minimally invasive lung cancer treatment. The advancements discussed included surgical tools, non-surgical techniques, and video-assistive technology. Qualtech also offers comprehensive Clinical Evaluation Report (CER) services to assist with medical device registration, drawing upon expertise in biomedical engineering and molecular biology to deliver high-quality reports for various regions.

• 2023-05-24 07:33:47

Qualtech's big topic article for this month's edition represents an overview of the recent and upcoming changes implemented in the ASEAN countries of Southeast Asia. We thereby cover 6 ASEAN countries and review the most critical and noteworthy changes, so that our readers remain up-to-date and can take required actions in a timeline manner.

• 2023-03-29 10:01:23

您是不是正在找尋一條進入各個亞洲市場的通路？
是不是想要簡單明瞭地取得各個東協國家之間的法規差異？
您是否有留意到東協醫療器材指令(ASEAN Medical Device Directive)將在進入多個東協國家之前予以簡化審查流程的機會？
想要了解更多、更廣、更全面的東協國家法規與市場資訊嗎？一同加入Qualtech的東協法規更新的線上研討會吧！研討會預計將於2023年4月28日下午4:00至5:30舉行，俗話說機會是留給有準備的人，所以，別錯過這次的精彩活動！

• 2023-02-23 02:33:41

Qualtech, in cooperation with Mr. Arkan Zwick of Austrian Manufacturer Croma-Pharma GmbH, have organized a webinar on the important updates pertaining to the EU MDR on February 7, 2023. Topics discussed include the European Commission's Proposal to extend the MDR transition period as well as the validity of MDD certifications, and our suggestions regarding the critical steps to be taken in order to smoothly obtain approval under the MDR. The content of the webinar has been briefly summarized in this article.