Workshop:
Improving efficiency using Real World Data
There is an increasing interest in using real world data for clinical trials. And that is for a reason. New technologies, availability, insights and better possibilities for protecting privacy makes it achievable to use this kind of data more and more.
During the workshop we will handle the different possibilities in which you can use real world data ranging from patient selection to using wearable data, automating source data upload, using real world data as a synthetic control arm and for study follow-up. We will talk about the usage, reliability, pitfalls and the importance of data engineering and statistics in using this data. In interactive breakout sessions you have the opportunity to explore this further in small groups and to meet fellow industry professionals.
We will also have Ella Jansen from the PHARMO Institute talk about the data sources they have available and the european data network that they are part of. In addition, Julia Kurps of The Hyve will tell more about uptake of data from commercial wearables and EHR systems.
This inspiring and interactive workshop will be online and live via zoom on Thursday 2 September 2021, 16:00-18:00 CET / 10:00-12:00 EST. The content of the workshops is provided for for free. However, we ask a small fee of € 25,- (including VAT) for registration and administration. This also assures a dedicated audience during the workshop. You can register for this workshop via the Register button below. When you are interested in the other workshops as well you can register for the full fall workshop cycle at a reduced fee.
Reactions of participants:
“Thank you very much for your training, I learnt a lot and I realized I need to learn even more ! It was very informative and well done.”
“Thanks for such a well run and interesting workshop. I learnt loads – especially about synthetic control arms. It was also great to see everyone participating.”
““The breakout sessions are good for networking, like speed dating”
About the trainer(s):
Berber Snoeijer started in clinical research in 1997 as a biometrician and has since then worked with clinical data in different functions. In 2001 she started a CRO, Biometric Support, aiming at the data management, data analysis and reporting of clinical trials. After selling this CRO, she switched in 2011 to work as a R&D manager dedicated to investigate and utilize the potential of real world data from electronic health records. This resulted in many different solutions including a full reporting system to give feedback information to clinical research professionals. For efficient processes and use of the data, she experienced and used the skills of technical (software and database) engineering, process engineering and improving efficient utilization and interactions of people based on management drives. Nowadays, she uses these skills and knowledge to assess, design and improve business solutions and processes on smaller and larger scale.
