Yes. There is no registration fee for the workshop

Yes. We welcome regulators from APEC member economies and non-APEC member economies. Please provide their emails to TFDAMDCOE@GMAIL.COM . We will send information to them.

• Please download and read the guidances from TFDA CoE website at https://tfdamdcoe.itri.org.tw/training.html These guidances are training materials for the workshop.
• We will request one participant from each regulatory authority to introduce the medical device regulation of its country. The PowerPoint template will be sent out in early August and we expect to receive the pre-record presentation slides on August 21.
• The practice of EP checklist will be open for participants from August 28 to September 11. Please remember to do the assignment and interact with other trainees.

We expect at most 2 to 3 participants from one organization, and in total 40-60 participants for the workshop. However, the number of participants is limited. Priority will be considered to regulators. The selection of workshop participants will be made after the registration closing date on July 26. The confirmation letter will be sent out on August 2.

You could register for the workshop on TFDA CoE website at: https://tfdamdcoe.itri.org.tw/Registration.html