Overview

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 at database lock and push back timelines.  

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 Biometrics, Director/Head Clinical Operations, Head/Team Manager Data Management, Head/Team Manager Data Programmers, Clinical Data Manager, Clinical Programmer, CDISC expert, Data Standard expert, Head Biostatistics, Head 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: healthscience@sgs.com

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