Assessment of risks
At ICON Development Solutions we always put the safety of our volunteers first. We, like other clinical research organisations, are governed by legal and ethical codes to ensure we comply with the guidelines on good clinical practice, good laboratory practice and good manufacturing practice.
All our studies are conducted under internationally agreed guidelines set down by the US Food and Drug Administration (FDA) and the UK Medicine and Healthcare Products Regulatory Agency (MHRA). Each study is reviewed by an Independent Ethics Committee who are responsible for ensuring that your safety has been thoroughly considered, that the information provided to you is fair, balanced and accurate and that your rights as a volunteer are maintained.
For your safety you must have a 3 month washout period between studies to ensure the study drug is clear from your system.