Education and training in October 2016
2016/10/01 14:00-16:30 The application of clinical trial and human research protection resources- Part 10
14:00-16:30 Introduction delegation form and case report form defect occur frequently and review points for human research
2016/10/15 13:00-17:00 Human research and clinical trial team work training course: GCP audit and Adverse event report
13:10-14:00 The conflict of interesting and risk assessment at clinical trial
14:00-14:50 Clinical trial, DSMP and DSMB
15:10-16:00 Bias report of clinical trial and how to improvement
16:00-16:50 Adverse event report of clinical trial and how to improvement
2016/10/19 16:00-18:00 The interview key point training for maintaining accreditation of AAHRPP site visit- Part 1
16:00-18:00 The interview key point training for maintaining accreditation of AAHRPP site visit
2016/10/21 11:00-13:00 The interview key point training for maintaining accreditation of AAHRPP site visit- Part 2
11:00-13:00 The interview key point training for maintaining accreditation of AAHRPP site visit
2016/10/22 13:00-17:00 Human research and clinical trial team work training course: GCP inspection
13:10-14:00 GCP inspection in EMA
14:00-14:50 Introduction international GCP inspection of Japan
15:10-16:00 Introduction international GCP inspection of FDA
16:00-16:50 The current situation and notice for Taiwan GCP inspection
2016/10/29 13:00-17:00 Human research and clinical trial team work training course: A new medical device product how to hit the market
13:10-14:00 Introduction Taiwan government law for to hit the market of a new medical device product and case discussion
14:00-14:50 Introduction China government law for to hit the market of a new medical device product and case discussion
15:10-16:00 Introduction USA government law for to hit the market of a new medical device product and case discussion
16:00-16:50 Introduction EMA government law for to hit the market of a new medical device product and case discussion