The Medicines (Administration of Radioactive Substances) Amendment Regulations 2006

law://uk/uksi/2006/2806@2026-11-13

Contents

1Citation, commencement and interpretation#

(1)These Regulations may be cited as the Medicines (Administration of Radioactive Substances) Amendment Regulations 2006 and shall come into force on 17th November 2006.

(2)In these Regulations “the principal Regulations” means the Medicines (Administration of Radioactive Substances) Regulations 1978.

2Amendment of regulation 1 of the principal Regulations#

In regulation 1 of the principal Regulations (citation, commencement and interpretation), in paragraph (2)—

(a)after the definition of “directions”, insert the following definition—“• “medical exposure” has the same meaning as in the Ionising Radiation (Medical Exposure) Regulations 2000;”

(b)after the definition of “notice”, insert the following definitions—“• “operator” has the same meaning as in the Ionising Radiation (Medical Exposure) Regulations 2000;• “practitioner” has the same meaning as in the Ionising Radiation (Medical Exposure) Regulations 2000;”

3Substitution of regulation 2 of the principal Regulations#

For regulation 2 of the principal Regulations (control of administration) substitute the following regulation—“2 1 No person shall administer to a human being (otherwise than to himself) any radioactive medicinal product unless he is a doctor or a dentist holding a certificate issued by the Ministers for the purposes of section 60 of the Act in respect of radioactive medicinal products (hereinafter referred to as a “certificate”) or a person acting in accordance with the directions of such a doctor or dentist.2 Paragraph (1) does not apply where the administration of a radioactive medicinal product would result in a medical exposure and the conditions specified in paragraph (3) are satisfied.3 The conditions referred to in paragraph (2) are that—a the medicinal product is administered by an operator acting in accordance with the procedures and protocols referred to in regulation 4(1) and (2) of the Ionising Radiation (Medical Exposure) Regulations 2000 which apply to the exposure referred to in paragraph (1);b that medical exposure has been authorised by a practitioner or, where it is not practicable for a practitioner to authorise the exposure, an operator acting in accordance with written guidelines issued by a practitioner;c the practitioner is the holder of a certificate; andd the medicinal product is not a controlled drug.4 Where a certificate is issued to a doctor or dentist specifying particular descriptions or classes of radioactive medicinal products—a the doctor or dentist holding the certificate;b any person acting in accordance with his directions; andc an operator acting pursuant to his authorisation of a medical exposure or in accordance with his guidelines,shall not administer any radioactive medicinal product unless it is a radioactive medicinal product of a description or falling within a class specified in the certificate.5 Where, in relation to a radioactive medicinal product specified in a certificate, the purpose for which the administration is also specified—a the doctor or dentist holding the certificate;b any person acting in accordance with his directions; andc an operator acting pursuant to his authorisation of a medical exposure or in accordance with his guidelines,shall not administer any radioactive medicinal product unless it is a radioactive medicinal product of a description or falling within a class specified in the certificate.6 Where a certificate issued to a doctor or dentist specifies both the persons to whom any descriptions or classes of radioactive medicinal product may be administered, and the descriptions or classes of radioactive medicinal product which may be administered—a the doctor or dentist;b any person acting in accordance with his directions; andc an operator acting pursuant to his authorisation of a medical exposure, or in accordance with his guidelines,shall not under that certificate administer any such description or classes of radioactive medicinal product except for the purpose of diagnosis or treatment of a person specified in that certificate.”

Contains public sector information licensed under the Open Government Licence v3.0.

The Medicines (Administration of Radioactive Substances) Amendment Regulations 2006

The Medicines (Administration of Radioactive Substances) Amendment Regulations 2006

1Citation, commencement and interpretation#

2Amendment of regulation 1 of the principal Regulations#

3Substitution of regulation 2 of the principal Regulations#

Defined terms · 4

Connections

History · 1 version

Key facts

1Citation, commencement and interpretation#

2Amendment of regulation 1 of the principal Regulations#

3Substitution of regulation 2 of the principal Regulations#