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Standards [CURRENT]

ISO 22127

Dosimetry with radiophotoluminescent glass dosimeters for dosimetry audit in MV X-ray radiotherapy
Edition 2019-12

Standards [CURRENT]

ISO 28057

Clinical dosimetry - Dosimetry with solid thermoluminescence detectors for photon and electron radiations in radiotherapy
Edition 2019-07

Solutions for practical implementation - Sample texts, templates, checklists
Edition 2016-08

Technical rule [CURRENT]

ISO/TR 24290

Health informatics - Datasets and data structure for clinical and biological evaluation metrics in radiotherapy
Edition 2023-05

Corrigendum to Regulation (EC) No 1394/2007 of the European Parliament and of the Council of 13 November 2007 on advanced therapy medicinal products and amending Directive 2001/83/EC and Regulation (EC) No 726/2004
Edition 2009-03-31

Administrative provision

2009/120/EG

Commission Directive 2009/120/EC of 14 September 2009 amending Directive 2001/83/EC of the European Parliament and of the Council on the Community code relating to medicinal products for human use as regards advanced therapy medicinal products
Edition 2009-09-14

Regulation

EGV 1394/2007

Regulation (EC) No 1394/2007 of the European Parliament and of the Council of 13 November 2007 on advanced therapy medicinal products and amending Directive 2001/83/EC and Regulation (EC) No 726/2004
Edition 2007-11-13

Administrative provision

EUB 2022/6

Commission Implementing Decision (EU) 2022/6 of 4 January 2022 amending Implementing Decision (EU) 2021/1182 as regards harmonised standards for biological evaluation of medical devices, sterilisation of health care products, aseptic processing of health care products, quality management systems, symbols to be used with information to be supplied by the manufacturer, processing of health care products and home light therapy equipment
Edition 2022-01-04

Corrigendum to Regulation (EU) No 1235/2010 of the European Parliament and of the Council of 15 December 2010 amending, as regards pharmacovigilance of medicinal products for human use, Regulation (EC) No 726/2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency, and Regulation (EC) No 1394/2007 on advanced therapy medicinal products
Edition 2012-07-27

Administrative provision

2014/3/EU

Commission Delegated Directive 2014/3/EU of 18 October 2013 amending, for the purposes of adapting to technical progress, the Annex IV to Directive 2011/65/EU of the European Parliament and of the Council as regards an exemption for lead acetate marker for use in stereotactic head frames for use with CT (Computed Tomography) and MRI and in positioning systems for gamma beam and particle therapy equipment
Edition 2013-10-18

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