Regulatory Compliance in UK Laboratories Processing Clinical Trial Samples: Guidance from a UK Regulatory Inspector

Date:29th September 3:00-4:30 p.m.

Venue: Webinar

This is a MHRA webinar offered in partnership with ACRP. This webinar will provide a rare opportunity to discuss your queries of Laboratory Compliance directly with Andrew Gray, Head of the United Kingdom Good Laboratory Monitoring Authority within the UK Regulatory Inspectorate Group of the MHRA.  The webinar will cover a range of key issues, such as sample shipping and receipt, the organisation and conduct of laboratory analysis, subject confidentiality, blinding and unbinding of clinical samples, expedited reporting of data, and lines of communication between the laboratory and the sponsor or clinical investigators.