offers software solutions which help streamline R&D processes of our customers:
Data Analysis and
Reporting Environment for fully controlled, traceable and
regulatory compliant process in clinical trials.
Mapping program and specification generator for
easy data conversion to CDISC and custom data models based on metadata definitions.
with a few mouse clicks from metadata-based element definitions.
ensure data consistency and compliancy
with standard and user-defined checks.
Java based tool for
content and structure validation of ODM files
including define.xml with 400+ built-in checks
Automatic test environment for operational qualification (OQ) and performance qualification (PQ) of SAS macros
In the pre-clinical area our product line includes:
Validated software package for the non-compartmental analysis of toxicokinetic and pharmacokinetic studies.
Laboratory Information Management System (LIMS)
supporting in-vivo and in-vitro as well as radioactive and non-radioactive studies.
Our clinical products as well as ToxKin are based on the
and 21 CFR Part
compliant, modular e-clinical solutions suite.
Professional Services for individual customer projects are a key element of entimo AG's core competencies. Find out more about our professional