s 41 Interpretation of Part 2
(1) In this Part— “the 2007 Regulations ” means the Human Tissue (Quality and Safety for Human Application) Regulations 2007; “the 2012 Regulations ” means the Quality and Safety of Organs Intended for Transplantation Regulations 2012; “ anatomical specimen ” means— the body of a deceased person to be used for the purpose of anatomical examination, or the body of a deceased person in the course of being used for the purpose of anatomical examination (including separated parts of such a body); “ appeals committee ” has the meaning given by section 20(2); “ designated individual ”, in relation to a licence, means the individual designated in the licence as the person under whose supervision the licensed activity is authorised to be carried on; “ export ” means export from England, Wales or Northern Ireland to a place outside England, Wales and Northern Ireland; “ import ” means import into England, Wales or Northern Ireland from a place outside England, Wales and Northern Ireland; “ scheduled purpose ” means a purpose specified in Schedule 1. (2) In this Part, references to the carrying-out of an anatomical examination are to the carrying-out of a macroscopic examination by dissection for anatomical purposes of the body of a deceased person, and, where parts of the body of a deceased person are separated in the course of such an examination, include the carrying-out of a macroscopic examination by dissection of the parts for those purposes. (3) In this Part, references to a person to whom a licence applies are to a person to whom the authority conferred by the licence extends (as provided by section 17).