• 2021-06-25 08:59:13

Qualtech Consulting would like to invite you to our free online Webinar on the subject of the ”China Medical Device Registration – New Regulation for Supervision and Administration of MDs (RSAMD)”, which has gone into effect on June 1, 2021.

• 2021-06-29 11:30:23

On 25th June, Qualtech and ISS AG jointly hosted an enriching webinar session on the newly implemented Medical Device Regulation MDR (EU) 2017/745 (MDR) and the dynamic European medical device landscape. In this article, we are looking at the important points discussed.

• 2020-10-28 02:13:28

With Overseas Medical Equipment Technical Assistants (OMETA), Qualteh has held an online seminar about regulatory updates in ASEAN on 27th October, where we covered major updates in the Philippines, Thailand, and Malaysia.

• 2020-08-13 02:21:04

The online event represents the third webinar in our 2020 series and will be held on September 30th (Wed), 2020 at 10:45am (UTC+8). Shall this Webinar be of interest to you or one of your colleagues, please be sure to register as soon as possible.

• 2020-05-14 09:43:07

The online event represents the second webinar in our 2020 series and will be held on June 17th, 2020 (Wednesday) at 11am (GMT+8). Shall this Webinar be of interest to you or one of your colleagues, please be sure to register under the following link (limited seats available).

• 2020-03-18 10:32:08

The ASEAN Common Submission Dossier Template (CSDT) makes it significantly easier to penetrate the ASEAN markets collectively. Therefore, do not miss the chance to learn about the benefits of the CSDT and what documentations are required for developing the Common Submission Dossiers.