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The HTA must receive an application before it can grant a licence. The same Designated Individual (DI) is appointed for all sites; and. • All sites work . C3 Staff involved in seeking consent receive training and support in the implications and.
1 Sep 2016 This Quality Manual, and appropriate training, will be made available to all .. It is important that all researchers work with the DI, PDs and HTA
(ethics-expired research samples of 'relevant material') and HTA Licence 12318 required to attend any training sessions that are advised by the DI. 9) I will
Relevant Material: The definition of relevant material in the Ht Act is: The DI must complete HTA accredited training to the HTA's satisfaction and within a.
1 Mar 2006 To explain the HTA's structure, ethos and functions; To summarise our Storage of material from a living person for a “specified purpose"; Public display sectors; Regulatory timetable - training for DIs, fees, inspections etc
Under the Act, the Designated Individual (DI) is responsible for licensed activities use of material from a deceased person for clinical audit, education, training,
10 Jan 2012 6.3 Deputy Designated Individual (Deputy DI) Registration and Training . specific training provided by the HTA to undertake this role and
Evidence-Based Medicine (Sackett 1997), a guide to the field, recently updated health problem, by a clinician with certain training, or in a specified treatment setting. Buckley DI, Ansari M, Butler M, Williams C, Chang C. Chapter 4.
they comply with the HT Act 2004 and the HTA's Codes of Practice & capture C3 Staff involved in seeking consent receive training and support in the implications and essential requirements of taking . Manager and DI in accordance with.
29 Jul 2016 The Quality Manual and Standard Operating Procedures (SOPs) will be .. The licence holder, with the consent of the DI makes the HTA licence application. . relating to human health (including training for research into

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August 2017