Governance

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ACCORD supports researchers to meet stringent research governance and regulatory requirements, and to fulfil legal, ethical and scientific obligations during the conduct of their research. As a single point of entry to professional advice and expert regulatory support, ACCORD has underpinned the institutions’ successful sponsor inspections by the Medicines and Healthcare products Regulatory Agency (MHRA).

Working as part of NHS Research Scotland (NRS), ACCORD offers central access to state-of-the-art clinical research infrastructure that facilitates the delivery of world-class research. It endeavours to provide rapid R&D approval times that meet ambitious national targets and enable prompt and efficient study start up. Its Quality Assurance and Clinical Trial Monitoring team maintain oversight of the research portfolio, acting to ensure that patient welfare is safeguarded, institutional risk is minimised and the highest research standards are upheld. Through ACCORD, NHS Lothian and the University of Edinburgh act as single sponsors or co-sponsors of clinical research led from Lothian.

For ECTU Trial Portfolio studies, ACCORD will delegate defined responsibilities to ECTU. 

ECTU has a suite of SOPs that cascade from the practices defined by ACCORD SOPs.  ECTU works closely with ACCORD to ensure regulatory compliance and a continuous process of quality improvement.

ACCORD - contact them here