The DIA meeting is a great opportunity to network with international leaders, influencers and regulators in the life sciences industry. This sharing of knowledge between experts and leaders promotes innovation and enhances the development of healthcare globally.
This is the perfect occasion to talk to Formedix about our industry-leading clinical trial metadata repository and design tools. Features are geared towards saving you time, money and effort whilst improving consistency and reusability of your submission ready metadata.
- Easy creation, management and reuse of your metadata assets
- Change control, life cycle and governance processes
- Impact analysis of change to studies and standards
- Automation of the SDTM conversion process with CDISC Define-XML 2.0
- Implementation of CDISC standards for easy compliance with regulations from FDA and PMDA
Join our experts Mark Wheeldon (CEO) and Darren Bill (Head of Operations), if you are interested in improving the consistency and reusability of your metadata.