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The CEO directorate is made up of the CEO, Human Resources (HR), and the Executive Assistant to the Chair, CEO and SMT.
The Regulations transposing EU import and coding Directives came into force on 1 April 2018. Changes to these Regulations affect all licensed establishments in the human application sector.
Two EU Directives have been implemented for the coding and import of tissues and cells for human application. These Directives are in force throughout the UK and have been transposed through the The Human Tissue (Quality and Safety for Human Application) (Amendment) Regulations 2018
How is the cord blood collected?
We inspect establishments licensed under the Human Tissue (Quality and Safety for Human Application) Regulations 2007 at least every two years.
Research establishments reported that they comply with the HTA’s licensing standards on consent.
The data we received in relation to governance and quality systems was positive. 98% of establishments reported having documented policies and procedures in place for all licensable activities.
20. Overall, establishments in the research sector were found to be compliant with the HTA’s licensing standards, with no shortfalls being identified in more than half of inspections. The following sections highlight the key areas against our standards which were identified as requiring further...