Statistical analyses are an integral part of product development and innovation management - both for medical devices and the Pharmaceutical sector. Our long years of experience allow us to find the matching algorithms. And we counsel you as a matter of course, when dealing with the software relevant application of clinical standards and regulatory requirements.
- Consultation, Programming and Integration of statistical methods
- Software Validation (Quality assurance from SAS programs, programming standards)
- CDISC conversion of clinical studies
- Development of industry-specific applications
- Introduction of SAS solutions (SAS Clinical Data Integration, JMP Clinical, SAS Clinical Standards Toolkit)
- Customized industry training on topics such as Software Validation or Macro programming