Regulatory Approval

The Regulatory process required to approve an Enterion^TM regional absorption study is straightforward. Quotient Clinical has performed over 100 Enterion studies, which have been approved by the Medicines and Healthcare products Regulatory Agency (MHRA) and independent ethics committees; and blanket approval for Enterion studies has been granted by the Administration of Radioactive Substances Advisory Committee (ARSAC). Typical Regulatory approval times are 15 days or less.