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!
More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!
MoreQualtechs will be holding a Webinar focusing on EU MDR on May 25, 2021.
We welcome all interested guests to join for free.
Due to Qualtech’s vast experience in the ASEAN regulatory field, Qualtech’s specialists have been cordially invited to speak on the medical device registration processes in Vietnam, Indonesia, and the Philippines at the ASEAN Healthcare Market Conference.
MoreOn February 25th, Qualtech organized a webinar and guided participants through the China medical device regulations. Our expert covered such topics as registration preparation, registration reviewing process, post-market process.
MoreThe German-based “Society for Promotion of East West Knowledge Transfer” had invited the experts of Qualtech to share their knowledge on the Taiwan registration processes for medical devices and pharmaceutical products to a number of high-ranking and selected attendees. Within a 90-minute session held on November 10th, Qualtech guided participants through the different Taiwan certification procedures and further elaborated on the clinical requirements in place for pharmaceuticals.
MoreTaiwan’s FDA has issued a Good Distribution Practice Guideline for Medical Devices. With the new guidelines getting into force in the near future, relevant distributors will be required to obtain a GDP certificate before they can legally distribute medical equipment.
MoreIt is Qualtech priority to deliver the most update and accurate news to our clients as well as performing as platform to all associated organization. OMETA is one of the organizations that has a lengthy association with Qualtech Corporation.
MoreJanuary 8th, 2020 has marked the day of Qualtech’s extensive workshop on the new European Medical Device Regulations (MDR) for its Taiwanese clients. The event provided its attendees with the latest updates on the MDR implementation before the end of the transition period on May 26, 2020.
MoreIt is honor for Qualtech to receive an invitation from Hujing College, USST for the program ‘Training and Exchange of Precision Medical Innovation Technologies under the Background of Comprehensive Health’ in Shanghai, China from 25th November to 8th, December 2019. Diversity group of trainees consisted of innovators and professors from Brazil, South Africa, Israel, and Singapore, where Qualtech ASEAN represents Malaysia and Thailand.
MoreIn the past weeks, Qualtech has participated in the following three events: MEDICA in Germany, the Design of Medical Device Conference in Shanghai and the OMETA Seminar in Osaka.
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