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Draft programme: Scientific afternoon symposium on Patient Experience Data in Clinical Trials

by Jens Harald Kongsø | Jun 23, 2019 | Event | 0 Comments

why, what, how and when to collect patient experience data in clinical trials as part of regulatory decision Organized by Clinical Trial Experience Data Academy (CTED Academy) in collaboration with Biopeople, Copenhagen Centre for Regulatory Science (CORS), European...

Five challenges in obtaining strong feedback from clinical trials and ways to overcome them

by Jens Harald Kongsø | Jun 16, 2019 | Exit-interviews | 0 Comments

When pharmaceutical companies have completed a clinical trial, they may want to organise a Result meeting with the attendance of participating investigators and study nurses/coordinators. At the Result meeting, representatives from the pharmaceutical company...

The value of generating early insights on your investigational product

by Jens Harald Kongsø, Pernille Clemmensen | Jan 18, 2018 | Exit-interviews | 0 Comments

When pharmaceutical companies develop new medicines, they are required to comply with regulatory requirements by reporting and publishing their clinical results. Adhering to these requirements incentivises pharma to design their trials, choose comparators and...