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We are now in the third year of a multi-year strategy stemming from a review that took place in 2017. At this time, the HTA undertook a fundamental evaluation of the extent to which our strategic approach protects public and professional confidence in the proper use, and quality and safety of,...
As an establishment, you should risk assess your supply chain of reagents and consumables relating to the handling of tissues and cells.
Under the Enterprise Act 2016, the HTA and all other statutory regulators have a duty to report against the Government’s Business Impact Target. The target for the 2015-2020 Parliament is a £10 billion reduction in the cost of regulation to business.
22. Two major shortfalls were found against the standard C1.
38. Four minor shortfalls were found against standard C3.
The HTA has a well-resourced fund for providing training to staff.
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