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QT ACTIVITY: Qualtech Shares Its Key Insights regarding China's New Regulations (RSAMD) via a Joint Webinar – JULY, 2021

QT ACTIVITY: Qualtech Shares Its Key Insights regarding China's New Regulations (RSAMD) via a Joint Webinar – JULY, 2021

  • 2021-08-02 06:36:08

On June 30th, Qualtech and ISS AG jointly hosted an online event informing far more than 100 different medical device manufacturers from all around the globe about China’s New Regulations. Qualtech’s team thereby detailed the important updates that the new RSAMD will bring, including the new obligations for product registrants under the nationwide adopted MAH system.

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QT Activity: CLINICAL EVALUATION REPORT (CER) SERVICES

QT Activity: CLINICAL EVALUATION REPORT (CER) SERVICES

  • 2021-06-24 02:55:03

We are happy to announce that Qualtech offers extensive services for Clinical Evaluation Report (CER) writing! Shall a CER be of interest for your business, please refer to the information within. Feel free to contact us for a first consulting session on this matter!

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QT ACTIVITY: Post-Brexit medical device regulatory landscape

QT ACTIVITY: Post-Brexit medical device regulatory landscape

  • 2021-06-04 09:34:53

In this webinar, you will learn more about Brexit and how Geopolitics affects medical device regulations. Our expert will introduce you to UKCA. Moreover, Ms. Fatehi will discuss the transitioning out period and will outline how the future for the U.K. market will look like.

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QT ACTIVITY: 2021年新醫療器材管理法實施重點研討會

QT ACTIVITY: 2021年新醫療器材管理法實施重點研討會

  • 2021-04-20 03:15:16

衛生福利部食品藥物管理署公告「醫療器材管理法」於110年5月1日正式實施。因應近期多項新法令之要求,理工科技顧問股份有限公司舉辦「2021年新醫療器材管理法實施重點」,協助廠商了解醫療器材新法令之要求及相關規定,並討論因應措施。報名日期自即日起至5月21日,額滿為止,敬請廠商踴躍報名!

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