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Bethesda North Marriott Hotel and Conference Center

2017年4月24日 (月) 午後 1:00 - 2017年4月26日 (水) 午後 4:30

5701 Marinelli Road, , North Bethesda, MD 20852 , USA

DIA/FDA Statistics Forum

The DIA/FDA Statistics Forum fosters open discussion of timely topics of mutual theoretical and practical interest to biostatisticians and clinical trialists.

Luncheon and Round Table Discussions

Session Chair(s)

Cristiana  Mayer, DrSc, PhD

Cristiana Mayer, DrSc, PhD

Head of Biostatistics

Johnson & Johnson Vision, United States

Attendees registered prior to the Early Bird rate deadline (April 18) will have an opporunity to pre-select their preferred tables to join.

Speaker(s)

Annie  Lin

Session Co-Chair

Annie Lin

Baxter, China

Pharmacovigilance Supervisor

Mouna  Akacha, PhD

Session Co-Chair

Mouna Akacha, PhD

Novartis Pharma AG, Switzerland

Group Head of Statistical Methodology

Shyla  Jagannatha, PhD

Session Co-Chair

Shyla Jagannatha, PhD

Janssen Pharmaceuticals Inc., United States

Scientific Director

Min  Min, PhD

Table 1: Innovative Strategies to Address Complex Study Design and Analysis Issues in Rare Disease Clinical Development

Min Min, PhD

FDA, United States

Mathematical Statistician, OB, OTS, CDER

Cristiana  Mayer, DrSc, PhD

Table 2: Modeling and Simulation in Drug Development: Best Practices and Current Challenges

Cristiana Mayer, DrSc, PhD

Johnson & Johnson Vision, United States

Head of Biostatistics

Zhong  Gao, PhD

Table 3: Statistical Issues in Biomarker Discovery, Validation, and Utilization in Clinical Trials

Zhong Gao, PhD

FDA, United States

Mathematical Statistician

Mouna  Akacha, PhD

Table 4: Choosing Measures of Treatment Benefit: Estimands and Beyond

Mouna Akacha, PhD

Novartis Pharma AG, Switzerland

Group Head of Statistical Methodology

Sue-Jane  Wang, PhD, MA, MS

Table 5: Biomarkers, How are they Discovered or Developed, and for What?

Sue-Jane Wang, PhD, MA, MS

FDA, United States

Mathematician Statistician

Shyla  Jagannatha, PhD

Table 6: Adaptive Predictive Enrichment Design: Experiences and Challenges

Shyla Jagannatha, PhD

Janssen Pharmaceuticals Inc., United States

Scientific Director

Changming  Xia

Table 7: Weighing Findings in Subgroup Analysis

Changming Xia

FDA, United States

Mathematical Statistician

Frank  Bretz, PhD

Table 8: Multiple Endpoints in Clinical Trials

Frank Bretz, PhD

Novartis , Switzerland

Distinguished Quantitative Research Scientist

Jimmy C. Wong

Table 9: Developing Standardized Tools for the Analysis of Clinical Trials

Jimmy C. Wong

FDA, United States

Statistical Analyst, Office of Biostatistics, OTS, CDER

Steve  Wilson, PhD

Table 10: Communication and Collaboration: Scientific Working Groups

Steve Wilson, PhD

FDA, United States

Senior Staff Fellow, OB, OTS, CDER

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