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The online registration is open for “2019 APEC Good Registration Management (GRM) Regulatory Science Center of Excellence Workshop”

【Update Date:2019-06-28unit:藥品組

  TFDA will hold 3-day 2019 APEC GRM Regulatory Science Center of Excellence Workshop in Taipei from Sep. 17th-19th, 2019. This workshop is approved by APEC Life Sciences Innovation Forum - Regulatory Harmonization Steering Committee (LSIF-RHSC). In order to assist in promoting regulatory science training of GRM in APEC, preparing good application dossier, and implement and integration of good review, we continue to use the past curriculum guidelines to train the trainer of industry-government-university this year.

  We invite international drug regulatory experts to introduce how to apply GRM to the entire product life cycle. Welcome to participate the plentiful activity.


【Dates】
  Sep. 17th, 2019 at 9:00-17:30   Welcome reception at 17:45-21:00

  Sep. 18th, 2019 at 9:00-16:30

  Sep. 19th, 2019 at 9:00-16:40
 

【Venue】Chang Yung-Fa Foundation International Convention Center
 
【Target Audience】Senior regulators or industry managers with at least 3 years of hands-on experience in regulatory review or submission.
 
【Agenda】http://www.raps-in-taiwan.org.tw/CoE_2019/2019_CoE_agenda.html
 
【On line registration】http://www.raps-in-taiwan.org.tw/CoE_2019/2019_CoE_contact.html
 
【Registration Dateline】July 31st 2019


2019 APEC Good Registration Management (GRM) Regulatory Science Center of Excellence Workshop