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news Ya-Wei - General | 2016-10-01 | Count:3128

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

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