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Danish Society for Biopharmaceutical Statistics

Meetings and courses


Joint FMS/DSBS Meeting, Statistical analysis of risks and safety data

November 1, 2016, Radisson Blu Hotel, Malmö


Program


The DSBS half-day seminar was held on 18 August 2016

Program and available presentations from the half-day seminar


Program Leader Leader Stijn Liis Loft


Joint DSBS/DSTS Two-day Meeting 10-11 November 2015

Program and available presentations from the two-day meeting


Program Program Mouna Mouna Anders Per Søren Lasse

Course material for Linear Mixed Models for Correlated and Repeated Measurements (March 2015)

Joint DSBS/FMS Meeting (October 2014)

DSBS meeting: Health Technology Assessment (May 2014)


Presentations at the annual general meeting (May 2014)


DSBS meeting: EMA draft guideline on the investigation of subgroups in confirmatory clinical trials (April 2014)


DSBS meeting: Statistical Issues in Drug development (October 2013)


Presentations at the annual general meeting (May 2013)


DSBS meeting: The statistician in a regulated and global industry - Experiences and challenges (January 2013)


Benefit-Risk Assessment Methodology Workshop, Statistical Issues in Medical Statistics, FMS/DSBS 5th Joint Workshop (2012)


Courses in Sample Size Determination in Clinical Trials and Meta analysis Using Individual Patient Data (January 2012)



Presentations at the annual general meeting (May 2011)


DSBS meeting February 21, 2011


Presentations at the annual general meeting (May 2010)


Statistical Issues in Medical Statistics, 4th joint workshop (April 2010)


Seminar on Regulatory Issues (May 2009)


Estimating Sample Size in Clinical Trials (April 2009)


The role of the pharmaceutical statistician (March 2009)


The Analysis of Incomplete and Longitudinal Data (October 2008)


Introduction to PK modelling with stochastic differential equations in R (May 2008)


Statistical Issues in Medical Statistics, 3rd Joint Workshop (April 2008)


Presentations at the annual general meeting (May 2007)


Group sequential and adaptive designs for clinical trials (May 2007)


Efficient design in phase II: Proof-of-concept studies and seamless progress to phase III (February 2007)


Seminar on Data Monitoring Commitee and safety (Annual general meeting, May 2006)


Statistical Issues in Medical Statistics, 2nd Joint Workshop (April 2006)


Clinical Trial Simulation (March 2006)


Multiple Testing: a clinical trial perspective (August 2005)


QT Prolongation (Annual general meeting, May 2005)


Non-linear mixed models analysis using the SAS system (November 2004)


Course in sample size calculation (September 2004)


Statistical Issues in Medical Statistics, 1st Joint Workshop (May 2004)


Follow up on Validation Workshop (January 2003)