As a service provider in the life science space we strive to adhere to an ever growing list of complex regulatory requirements. Our experienced quality and compliance experts regularly advise organisations such as the Clinical Trials Transformation Initiative and the Avoca Quality Consortium – adding Clinithink’s voice to the collective drive for more efficient (and effective) clinical research. As a technology-focused company we also ensure we combine our regulatory compliance knowledge and expertise with a future-proof approach, so that we can continue to play a part in improving the clinical research landscape for the long term.

Clinithink works within a Quality Management Framework and encourages continuous process improvement. Our services fall outside of Good Clinical Practice guidance and we have met with the Medicines and Healthcare products Regulatory Authority (UK) to discuss our current regulatory position. We intend to seek regulatory advice in the USA & India in 2020.