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Any activity carried out under an HTA licence needs to be under the supervision of a DI. If you wish to carry out the activity of procurement at an organisation that is already licensed by the HTA you will need to contact the DI and ensure that they are willing and able to supervise the activity...
We use the term ‘inspection’ to describe when we visit an establishment to meet with staff, view premises and facilities, and review policies and procedures.
You should read the relevant guidance document before you start to fill in the application form.
The guidance documents will tell you:
The HTA licenses a number of activities relating to human tissue. We are also responsible for carrying out inspections to ensure licence conditions are being met. These activities are laid out in the Human Tissue Act and associated Regulations.
The activities licensed by the HTA are:
Tissues and cells removed directly from a person are relevant material under the HT Act. Cell lines are not relevant material as all the original cells from the person have been replaced by cells that have divided and therefore have been created outside the human body.
The Human Tissue Act 2004 licenses (amongst other activities) the storage of relevant material for use for research. The Human Tissue Act explicitly excludes from its remit the licensing of material if it is created outside the human body. Therefore, the regulation of cell lines for research...