Dianthus Medical Limited

Dianthus Medical can help you with the writing of study protocols, ensuring that:

• The methodology and planned statistical analyses are optimised for the specified study objectives
• The protocol is free of all possible ambiguities that might impinge on the conduct of the study
• The study will adhere to guidelines for Good Clinical Practice (GCP) and other ethical considerations
• Your clinical trial has the best chance of being approved by the appropriate International Ethics Committee (IEC) or International Regulatory Board (IRB)

We can also assist in the design of your study.