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(h)

the circumstances in which the Supplementary Prescriber should refer to, or seek the advice of, the medical practitioner or dentist who is a party to the plan;

8.15.2

he has access to the health records of the Patient to whom the plan relates which are used by any medical practitioner or dentist who is a Party to the plan;

8.15.3

if it is a prescription for a medicine, the medicine is not a controlled drug within the meaning of the Misuse of Drugs Act 1971;  

8.15.4

if it is a prescription for a drug, medicine or other substance, that drug, medicine or other substance is not specified in any directions given by the Secretary of State under section 28U of the Act as being a drug, medicine or other substance which may not be ordered for Patients in the provision of medical services under the Contract;

8.15.5

if it is a prescription for a drug, medicine or other substance, that drug, medicine or other substance  is not specified in any directions given by the Secretary of State under section 28U of the Act as being a drug, medicine or other substance which can only be ordered for specified Patients and specified purposes unless:

(a)

the Patient is a person of the specified description,

(b)

the medicine is prescribed for that Patient only for the specified purposes, and

(c)

when giving the prescription, he endorses the face of the form with the reference SLS;

8.15.6

if it is a prescription for a medicine:

(a)

the medicine is the subject of a product licence, a marketing authorisation or a homeopathic certificate of registration granted by the licensing authority or the European Commission, or

(b)

subject to Clause 8.17, the use of the medicine is for the purposes of a clinical trial, and either that trial is the subject of a clinical trial certificate issued in accordance with the Medicines Act 1968, or a clinical trial certificate is not needed in respect of that trial by virtue of any exemption conferred by or under that Act,

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