In this newsletter:
- PHUSE Single Day Event in Frankfurt
- OCS Consulting wins at the 2025 SAS® Global Partner Awards
- SAS® accredited trainer
- Unlocking the Power of Real-World Data for Regulatory Submissions
PHUSE Single Day Event in Frankfurt
On March 13th the next PHUSE Single Day Event in Frankfurt takes place. The theme is ‘Bridging Tradition andInnovation – Integrating the Best of the Old and New Worlds in Clinical Trial Development'.
Explore how traditional practices like SAS programming and CDISC standards mapping are integrating with open-sourcetools like R and Python to enhance clinical trials. Discover how AI and machine learning improve data mappingefficiency, statistical analysis and visualization, to drive more insightful trial outcomes. Register here for the event.
OCS Life Sciences will contribute with a presentation together with its partner Clinline:
Berber Snoeijer (ClinLine) and Javier Rodriguez Soto (OCS Life Sciences) will present the topic:
‘Bridging the Standards: Standardised Mapping and Lineage’
Data mapping in clinical research lacks a universal standard, often resulting in inefficiencies and inconsistencies. Thispresentation introduces an open-source tool that improves data lineage, FAIRness, and automation, streamlining themapping process for clinical trial and real-world data. Using real-world examples, we will demonstrate how this toolenhances transparency, automation, and reproducibility in clinical trial and real-world data mapping acrossmultiple transformation steps.
We hope to see many of you there! If you can’t make it to the event but are interested in this presentation, please get intouch with us.
OCS Consulting wins at the 2025 SAS® Global Partner Awards
SAS recently shared the winners of its 2025 Global Partner Awards. Theannual awards celebrate SAS Partners who have shown impressive growthand dedication with SAS, leveraging the capabilities of technologies like SAS Viya®, SAS’ cloud-native data and AI platform, to grow their businessand deliver results across industries.
We are proud to announce that OCS Consulting has been namedSolution Provider Partner of the Year – Western Europe at the 2025 SASGlobal Partner Awards. This recognition is particularly special to us as wehave now won such an award for the second year in a row. It highlights ourdedication to delivering innovative solutions and driving business successwithin the Life Sciences market with SAS software.
Winning this award again is an acknowledgement to the dedication andexpertise of our entire team. It is a recognition of the collective efforts of ourorganisation, and we are delighted with the result. We look forward tocontinuing our strong partnership with SAS and helping our clients harnessthe power of data and AI to drive success.
A big thank you to SAS and our remarkable team for making thispossible!
SAS® accredited trainer
We're delighted to announce that our colleague Lieke Gijsbers is now a SASaccredited trainer. Congratulations to Lieke!
Lieke is now eligible to provide training on behalf of SAS on a variety oftopics, including SAS Life Science Analytics Framework (LSAF). In themeantime we have delivered a first SAS LSAF training for a client inDenmark.
Unlocking the Power of Real-World Data for Regulatory Submissions
As Real-World Data (RWD) becomes increasingly important in regulatory submissions, ensuring data quality, traceability, and compliance is essential. However, with data coming from diverse sources—such as registries, electronic health records, and insurance claims—each with unique collection methods and standards, navigatingthis process can be complex.
To address this challenge, OCS Life Sciences and ClinLine have partnered to help organisations integrate RWD intoclinical trial submissions efficiently and in compliance with regulatory requirements.
Our Services
We ensure a complete data lineage from source to submission by offering:
- Data Source Requirements – Identifying suitable RWD sources based on study objectives
- Data Source Assessment – Evaluating data quality, relevance, and representativeness
- Standardization & Mapping – Aligning RWD with SDTM, OMOP, FHIR, USDM, and other industry standards
- Data Analysis & Reporting – Preparing RWD for regulatory use
- Traceability & Documentation – Ensuring full transparency and compliance
Why Choose Us?
Our team of consultants, programmers, and statisticians brings:
- Deep expertise in RWD and clinical trial processes
- Proven experience in industry standards and study mapping