entimo news archive entimo has a long history, This is it. 2019 2018 2017 2016 2019 Release of entimICE® FastTrack 3.1 strengthens integration 01-01-2025 Just weeks after the 3.0 release, entimo has updated its integrated CDR/SCE entimICE FastTrack to version 3.1. System users now can benefit from additional interfaces, including connections to Veeva Vault EDC, Posit Workbench and Lixoft Monolix/Simulx. The...

entimICE® DARE Success with Data entimo Integrated Clinical Environment entimo's flagship product is a modular enterprise software suite for the clinical development process. It consists of a metadata driven Statistical Computing Environment (SCE) with a tightly integrated Clinical Data Repository (CDR) and a Metadata Repository (MDR). entimICE is unrivaled in the market for out of the box functionality and configurability to adjust to evolving customer demands. It provides superior adaptation...

entimo moves up in environmental rating entimo’s 2025 Climate Change rating from CDP (formerly the Carbon Disclosure Project) has improved significantly compared to 2024, and now stands at a B level. This marks meaningful progress in our environmental transparency and climate action efforts. A rating at this level recognizes verified, evidence-based climate action and shows that entimo has moved from awareness into meaningful implementation. This is also the highest score a company can achieve without public CDP disclosure, and it highlights not only our progress, but the strength of...

Inside the 33rd BVMA Symposium: Reflections from entimo’s CEO Marc Jantke The 33rd BVMA Symposium in Munich brought together an extraordinary cross-section of Germany’s clinical research landscape including industry leaders, regulatory agencies, CROs, sponsors, NGOs, and government representatives. For entimo’s CEO, Marc Jantke, it was his first time stepping into what some attendees call a “class reunion.” As it turned out, the nickname was more accurate than he expected.   BVMA Symposium Recap Marc describes the opening get-together as “a fantastic opportunity to connect with...

Your tech ally for fast and compliant clinical research About entimo We support scientific rigor and speed research by lifting the compliance burden from researchers’ shoulders. Contact us Entimo AG is a German life sciences informatics company that provides software solutions and services to biopharmaceutical and contract research organizations. Our software and services address regulatory requirements in clinical research and development. We use state-of-the art technical approaches to...

Fasttrack your submission with entimICE FastTrack entimICE FastTrack Statistical Computing Environment significantly increases the efficiency of the clinical data science processes, managing constantly growing study pipelines, resource bottlenecks, and ever-increasing regulatory requirements. entimICE FastTrack is ready today for data from decentralized clinical trials and various sources, and fully supports real-time analysis and reporting along with the use of...

GxP compliant clinical trial analysis and reporting entimICE FastTrack in use Book a demo Your profile You are working with a pharma or biotech company with an active phase II/phase III clinical trial pipeline. Your clinical data science ecosystem is overly complex or outdated, in the worst case both. Your daily business processes are disconnected and inefficient and your clinical trial teams blocked by the inability to use the best tools for the tasks at hand. Your challenge Accelerating the timeline from...

Enabling open source for regulatory activities entimICE FastTrack in use Book a demo Your profile You are working for a biotech or pharma company with an active Phase III clinical trial pipeline, or for a CRO providing biometrics services to sponsors. Your teams are engaged to make use of R in clinical trial reporting activities, in combination with SAS or as a replacement for SAS. Your challenge The use of open-source technologies such as R and Python in clinical R&D has been growing steadily for years,...

Enabling open source for non-regulatory activities entimICE FastTrack in use Book a demo Your profile You are working with a pharma or biotech company with active real-world evidence projects. Your company has an established Phase II/Phase III clinical trial pipeline, and you are looking to smooth the transition between real-world research and clinical trial research. Your challenge Open-source technologies such as R and Python have long been used in real-world research. As their adoption in clinical research...

Multi-sponsor management for CROs entimICE FastTrack in use Book a demo Your profile Data management and biometrics teams involved in clinical trials across multiple sponsors often work with a mix of systems—some provided by the sponsor, others based on their own internal setups. Each sponsor typically enforces their own SOPs, requiring your CRO to adapt its processes and tools to meet different expectations. This requires a high level of flexibility from CRO teams to ensure compliance and efficient...

Collaboration with CROs entimICE FastTrack in use Book a demo Your profile You are working for a small-to-midsized biopharma (SMB) or a biosimilars generics pharma company with a few clinical trials. Your company is outsourcing most activities to CROs, and your small biometrics team manages many deliveries from multiple different CROs simultaneously.  Your challenge SMB biopharma and biosimilars generics pharma companies often fully outsource the management of clinical trials to CROs, typically working with a...

entimICE® FastTrack Fast-track your submission The first cloud-native compliant SCE for clinical research Contact us Faster statistical computing environment entimICE FastTrack statistical computing environment significantly increases the efficiency of clinical data science processes, managing constantly growing study pipelines, resource bottlenecks, and ever-increasing regulatory requirements. entimICE FastTrack is ready today for...

German precision Global trust Faster submissions entimo simplifies complex clinical ecosystems with trusted, audit-ready solutions and a people-first approach. Contact Contact Leader in life sciences technology Entimo is a pioneer in life sciences information technology, built on a foundation of precision, reliability, and quality—hallmarks of the “Made in Germany” standard. With more than 20 years of experience, we deliver future-ready software and expert services that simplify complex clinical research, enabling...

entimo Presents at PHUSE US Connect 2025 Jörn Bilow (l) and Marc Jantke welcome visitors to the entimo booth at the 2025 PHUSE US Connect. In March, entimo representatives joined industry colleagues at PHUSE US Connect in Orlando, Florida to drive conversations around innovations in SCEs and clinical data standards. Three from entimo delivered presentations, while the company sponsored the conference’s poster session. entimo CEO Marc Jantke talked about the potential use of AI to overcome the validation burden for open-source packages. The talk discussed how LLMs can be used...