Go/No Go decisions for subsequent development phase
Regulatory market authorisation
Market access and health technology assessment
At ClinMed Pharma our Biostatistics and Data Management team are most proficient in statistical modelling, programming and data collection methodology. We have a 21 CFR Part 11 compliant in-house developed readily interfaceable eCRF system that has been used by many of our customers. Our programmers are also well acquainted in developing eCRFs using the commercially available platforms.
In our pursuit to ensure competency remains ahead of opportunity, the Biostatistics and Data Management team are leading the effort on the leveraging of ‘Big Data’, Block Chain and the role of artificial intelligence.