ClinLine Open Archive
PHUSE EU Connect, 16th – 19th of November, Hamburg
– ClinLine presentation: Using CDISC USDM and BCs to select data from alternative data sources for regulatory purposes
– ClinLine paper: Click to explore the full paper and gain valuable perspectives
BioTechX, 6th – 8th of October, Basel
– ClinLine presentation: Mastering the Jungle of Real-World Data.
Mission Possible TransCelerate, 24th of September, Basel and New Jersey, US
– Poster: The Unified Study Definitions Mode (USDM) stores all information related to the study design. This includes the information noted in a study protocol, and additional details that are beneficial for downstream processes. The information stored in USDM can directly be used to create the SDTM trial design domains as is shown by the mappings that are available in the CDISC DDF-RA Github. At ClinLine, we have transformed these mappings to JSONata code which directly can be used to query the USDM JSON API files. The corresponding open-source python tool executes the JSONata code and subsequently creates the corresponding SDTM domains.
COSA Spotlight Q3 2025, 23rd of September 2025, Online
– ClinLine presentation: USDM to SDTM TS Domains. This presentation, part of the COSA Spotlight webinar, introduces the new open-source USDM to SDTM mapping tool now available on COSA.
PHUSE CSS Conference, 20th and 21st of May 2025, Utrecht, The Netherlands
– Clinline Poster: Unravelling the secrets of Real-World Data. ClinLine presented a poster showing how we handle real-world data and show corresponding lineage with our Parkinson use case.
CDISC EU Interchange, 14th and 15th of May 2025, Geneva, Swiss
– This presentation shows how we store the mapping information to ensure data lineage and FAIRness, and to improve the efficiency in the mapping process from source to submission datasets. We will illustrate this by updated examples of our Parkinson mapping project using the OCS mapping engine and ClinLines open source lineage tool.
Risklick Webinar, 24th of April 2025, online
– Here is the recording of our webinar “How to Standardize Clinical Trial Protocol Content Across your Company?”: Webinar Video
PHUSE Single Day Event, 13th of March, Frankfurt, Germany
– Presentation: Bridging the standards: standardized
mapping and lineage, Berber Snoeijer, ClinLine and Javier
Soto, OCS Life Sciences
EU Connect 2024, November 2024, Strassbourg, France
– From source to submission: Getting the best of multiple standards. Berber Snoeijer ClinLine and Jules van der Zalm, OCS Life Sciences. View slides or paper.
– Presentation: Ensuring governance and traceability of Real-World Data from source to regulatory submission: A Use case. Mike Kolzet, Eqty Life sciences and Berber Snoeijer, ClinLine. View slides or paper.
TransCelerate Digital Data Flow Solution Showcase, Webinar 26 September 2024, virtual
– Utilizing USDM to unlock Real-World Data Potential. Berber Snoeijer, ClinLine and Ali Dootson, Eqty Life Sciences, View recording.
SDE, June 2024, Heidelberg, Germany
– Experienced and Best Practices in Re-Using Real-World Data for Regulatory Purposes, Caro Sluijter, OCS Life Sciences, Berber Snoeijer, ClinLine. View slides
CSS, June 2024, Sliver Spring, US
– Digital Data Flow: Digitalizing Clinical Protocol Information to Accelerate Clinical research and Pharma to Healthcare Interoperability., TransCelerate/CDISC, View poster.
US Connect, February 2024, Bethesda, US
– Real-World Data: What is fit for purpose?, PHUSE Real-World evidence Quality and Reusability of Real-world data project members. View poster.
EMEA SDE September 2023, Utrecht, The Netherlands
– Insights into the TransCelerate Digitial Data Flow Initiative and the corresponding CDISC USDM data model, Berber Snoeijer, ClinLine. View slides.
CSS, September 2023, Silver Spring, US
– Assessing relevance and provenance of real-world data, Berber Snoeijer, ClinLine. View poster.
SDE Heidelberg, 22 June 2023
– Mitigating the challenges of real-world data usage and linkage in regulatory submission trials, Berber Snoeijer, ClinLine in cooperation with Achilleas Zaras and Nathan Johnson, eClinical solutions. View slides.
– Interoperability and automation: How we handle the increasing complexity of Data Sources. View slides.
– Hands-on workshop: efficiently and effectively migrating to a new environment, Guy Garrett, Achieve Intelligence and Berber Snoeijer, ClinLine
– Real-world data linkage and mapping: options and pitfalls
Berber Snoeijer, ClinLine. View slides
Xtalks Webinar – 16 June 2022
– Automating an End-to-End Clinical Data Workflow with a Platform Approach; Nathan Johnson, eClinical Solutions; Berber Snoeijer, ClinLine. View recording.
– A look into the Future of Clinical Data Processing and Analysis
Berber Snoeijer, ClinLine. View slides
EMEA Winter SDE 2021:
EU Connect November 2021:
– Data Ecosystems 2.0: The Data-Fluid Organization. Achilleas Zaras, eClinical Solutions + Berber Snoeijer, ClinLine. Available slides.
– The Real-World Eligibility check: How to create a FAIR SAS tool.
On-demand presentation by Berber Snoeijer, ClinLine. Available recording.
– Real-World Evidence hands-on Workshop. Stijn Rogiers and Sherrine Eid, SAS Institute and Berber Snoeijer, ClinLine. Available recording.
EMEA Spring SDE May 2021, virtual:
– How to scale up productivitiy and minimize efforts in clinical programming. Berber Snoeijer, ClinLine. Available slides.
Virtual SDE Beerse October 2020 , Belgium:
– Assessing the Impact of Governmental Interventions in Response to COVID-19 on Global Mobility. Mariska Burger, OCS Life Sciences and Berber Snoeijer, ClinLine. View recording
Virtual EU Connect November 2020:
– Use of unlimites real world data sources in clinical trials and how it changes the landscape. Berber Snoeijer, ClinLine
– Team performance and Drives, Workshop by Aart Brezet, Drives@Work. View Recording.
FIGON Dutch Medicine days December 2020:
– Improving clinical trial efficiency by using a real-world eligibility check
Berber Snoeijer, ClinLine. View poster, View recording