Join our live webinar to gain insight into handling bioanalytical and laboratory data in double-blinded trials.
Time is precious in clinical research, as demonstrated by the development of COVID-19 vaccines. Processing complex unblinded clinical data, such as immunology data in a double-blinded trial, can become critical during database lock and pushback.
Objective
By attending this webinar, you’ll gain valuable insights and practical tips for handling bioanalytical and laboratory data in double-blinded trials. This knowledge will help you ensure high-quality data and ultimately avoid delays leading to faster study completion.
Network with experts in the field and get your questions answered.
Agenda
- Introduction
- Common pitfalls in dataflows that can delay timelines
- Key success factors in handling unblinding data
- Real case study examples
- Q&A
Target Audience
The webinar is aimed at clinical research professionals looking to handle unblinded dataflow and optimize clinical trial timelines, such as director/head of biometrics, director/head of clinical operations, head/team manager data management, head/team manager data programmers, clinical data manager, clinical programmer, CDISC expert, data standard expert, head of biostatistics, head of pharmacokinetics and vendor manager.
Language: English
Cost: No charge
Can't make a live session? Register now and receive a complimentary recording after the live event.
For further information, please contact:
Stacy Dethier
Marketing Manager
t: +32 15 273 245