Regulatory and Consultancy

Our clients benefit from close, one-to-one support and direct contact with our scientists. Whether you require specific advice or a more integrated approach, our team will help you achieve your goals.

We have long established relationships with experts that use a variety of software tools. The technology is recognised by regulatory agencies and can be employed for in silico mutagenicity assessments. Our team has the depth of knowledge needed for confident analysis, as well as extensive experience of performing assessments on a wide range of substances and products.

We have the knowledge and expertise to advise on the CMC content of clinical trial applications, with subject matter experts on-site to assist with scientific advice. By collaborating with the on-site isotope labelling team, we are also able to provide regulatory dossiers for clinical trials designed to study the absorption, metabolism and excretion of radiolabelled pharmaceuticals.