Regulation 294 General requirements

relates to a medicinal product; and

is wholly or mainly directed at persons qualified to prescribe or supply such products.

subject to F1paragraphs (2C) and (3), it contains the particulars set out in paragraphs 1 to 8 of Schedule 30; and

in the case of a written advertisement, it is in accordance with paragraph 9 of that Schedule.

the particulars set out in paragraphs 2 to 6 of Schedule 30; and

the statement “Information about this product, including adverse reactions, precautions, contra-indications, and method of use can be found at:”; accompanied by

a website address that corresponds to that statement.

the particulars set out in paragraphs 1 to 8 of Schedule 30; or

a copy of the summary of the product characteristics.

does not apply to an advertisement to which regulation 295 (abbreviated advertisements) applies;

does not apply to oral representations made by medical sales representatives to which regulation 299 (medical sales representatives) applies; and

is subject to regulations 296 (exception for advertisements intended as a reminder) and 301 (advertisements for registered homoeopathic medicinal products).

in Northern Ireland only, the requirements of this regulation must be met in relation to the product for sale or supply in Northern Ireland,

in Great Britain only, the requirements of this regulation must be met in relation to the product for sale or supply in Great Britain, and

in the whole of the United Kingdom, the requirements of this regulation must be met in relation to both—