327.—(1) An inspector may inspect anything mentioned in paragraph (2)—
(a)in order to determine whether there has been a contravention of any provision of these Regulations which the enforcement authority must or may enforce by virtue of regulations 323 and 324;
(b)for the purpose described in regulation 325(1)(b) (verification of data at the request of the European Directorate for the Quality of Medicines and Healthcare); or
(c)in order to verify any statement made by an applicant for a manufacturer’s or wholesale dealer’s licence, marketing authorisation, certificate of registration, traditional herbal registration or Article 126a authorisation in an application under Parts 3 or 5 to 8.
(2) The things mentioned in paragraph (1) are—
(a)a substance or article appearing to the inspector to be a medicinal product;
(b)an article appearing to the inspector to be—
(i)a container or package used or intended to be used to contain a medicinal product, or
(ii)a label or leaflet used or intended to be used in connection with a medicinal product;
(c)plant or equipment, including computer equipment, appearing to the inspector to be used or intended to be used in connection with the manufacture, assembly, importation, sale, supply or advertising of, or wholesale dealing in, medicinal products;
(d)any process of manufacture or assembly of medicinal products;
(e)the way in which medicinal products, or the materials used in the manufacture of medicinal products, are tested at any stage in the process of manufacture or assembly; and
(f)information and documents relating to the manufacture, assembly, importation, sale, supply or advertising of, or wholesale dealing in, medicinal products;
(g)information and documents relating to the safety of medicinal products, including information and documents relating to compliance with—
(i)conditions imposed under any of regulations 59 (conditions of UK marketing authorisation: general), 60 (conditions of UK marketing authorisation: exceptional circumstances), 61 (conditions of UK marketing authorisation: new obligations post-authorisation) or 105 (conditions of certificate of registration),
(ii)the requirements of Part 11 (pharmacovigilance),
(iii)obligations and conditions under Articles 10a(1), 14(7) or 14(8) of Regulation (EC) No 726/2004, and
(iv)the requirements of Chapter 3 (pharmacovigilance) of Title II of Regulation (EC) No 726/2004.
(3) The inspector may for the purposes specified in paragraph (1) take or purchase a sample of a substance or article which appears to the inspector to be—
(a)a medicinal product which is, or is intended to be, sold or supplied; or
(b)a substance or article used, or intended to be used, in the manufacture of a medicinal product.
(4) The inspector may for the purposes specified in paragraph (1) require a person carrying on a business which consists of or includes the manufacture, assembly, importation, sale, supply or advertising of, or wholesale dealing in, medicinal products, or a person employed in connection with such a business, to produce information or documents relating to the business which are in the person’s possession or under the person’s control.
(5) The inspector may take copies of information or documents—
(a)inspected under sub-paragraph (2)(f) or (g); or
(b)produced under paragraph (4).
(6) The inspector may seize and retain a substance or article appearing to the inspector to be a medicinal product if the inspector reasonably believes that an offence under these Regulations is being or has been committed in relation to, or by means of, that substance or article.
(7) The inspector may, if the inspector reasonably believes that it may be required as evidence in proceedings, seize and retain—
(a)any document; or
(b)anything inspected, or discovered in the course of an inspection, under paragraph (1).
(8) The inspector may, if necessary, require a person who has the authority to do so—
(a)to open a container or package;
(b)to open a vending machine; or
(c)to allow the inspector to open a container, package or vending machine,
for the purpose of enabling the inspector to seize a substance, article, document or other thing under paragraph (6) or (7).
(9) The information and documents referred to in this regulation include any that are stored electronically.