QT Activity: Seminar on MDR Technical Document on 13th Dec. 2018 in Taipei - Oct, 2018
- 2020-02-12 14:16:42
海外医機器技術協力会(OMETA), Japan Association of Medical Device Industry (JAMDI), DEKRA Japan, and Qualtech Japan are jointly organising an upcoming seminar in early July (July 6th, 2018) in Japan.
MoreTaiwan Food and Drug Administration(TFDA) is organizing an upcoming seminar in end of July (July 20th, 2018) in Taoyuan (Taiwan), and Qualtech has been invited to share our GCP experience in China. This seminar will discuss the GCP inspection of medical devices in various oversea countries and how to conduct a multicenter clinical trial in various countries.
MoreWe are pleasure to share the successful seminar which had been held on July 10th by Japan Analytical Instruments Manufacturers' Association(JAIMA),
MoreWith a solid business foundation dating back to 1968, TÜV SÜD Japan was established in 1993 to meet the increasing demand for enhanced quality and safety testing and certification in the Japanese market.
MoreQualtech TFDA manager is invited to be the speaker in Singapore seminar "Understanding Taiwan's Regulatory Framework for Medical Devices" organized by Singapore Manufacturing Federation and DH RegSys Pte Ltd.
MoreOn 25 June & 26 June, 2013, Qualtech TFDA manager, Juliana Chang, was invited by Singapore Manufacturing Federation and DH RegSys Pte Ltd to give the TFDA training in Singapore.
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