Clinical trials in phases II-IV
In carrying out clinical trials in phases II-IV we:
- Obtain the regulatory documentation from the authorities
- Plan the design of the trial
- Write the protocol and the case report form
- Analyse and select centres according to the nature of the study
- Organise the start-up meeting
- Deliver, store and account for the stock of the study drug and other study materials
- Conduct a statistical analysis of collected data