Regulation 3(1)
1. The name and address of the applicant, and, where the applicant is not the proposed licensee, the name and address of the proposed licensee.
2. The period for which the licence is desired, where it is for less than five years.
3. A statement of the manufacturing or assembling operations to which the licence is to relate, including a statement whether they include one or both of the following—
(a)the manufacture of medicinal products, or
(b)the assembly of medicinal products.
4. A statement of the use for which the medicinal products are or are proposed to be manufactured, or assembled and whether the use is as stated in one or more of the following subparagraphs—
(a)for use by being administered to human beings,
(b)for use by being administered to animals,
(c)for use in the form of an ingredient in the preparation of a substance or article which is to be administered to human beings or animals for a medicinal purpose, or
(d)for use by incorporation in any animal feeding stuff.
5.—(1) The address of each of the premises where the manufacturing or assembling operations to which the application relates, or both operations, including any testing associated with manufacture or assembly, are or are to be carried out.
(2) The address of each of the premises if different from those referred to in the preceding subparagraph—
(a)on which are to be kept any living animals, or
(b)on which are to be kept or from which are to be obtained any materials of animal origin,
from which, in either case, are to be derived any substance or substances used in the production of the medicinal product whether human or veterinary to which the application relates.
(3) The address of each of the premises where the proposed licensee proposes to store medicinal products or from which he proposes to distribute them.
(4) A statement indicating the facilities and equipment available at each of the premises for storing the medicinal products on, and distributing them from or between, such premises.
(5) A separate statement in respect of each of the premises, of the manufacturing or assembling operations capable of being carried out at those premises with their existing facilities. Each statement shall specify the classes of medicinal products to which the operations are relevant.
(6) A separate statement in respect of each of the premises, of equipment available at those premises for carrying out each stage of the manufacturing or assembling operations described in subparagraph (5) of this paragraph.
6. A statement of any manufacturing operations, other than those to which the manufacturing licence is to relate, that are carried on by the proposed licensee on or near each of the premises referred to in paragraph 5 of this Schedule, and of the substances or articles which are the subject of any such operation.
7.—(1) The name and address and qualifications and experience of the production manager or other person whose duty it will be to supervise the production operations at each of the premises referred to in paragraph 5 of this Schedule, and the name and function of the person to whom he is responsible.
(2) The name and address and degrees, diplomas or other qualifications and experience of the person to be in charge of quality control over all the premises referred to in paragraph 5 of this Schedule and the extent of the authority to be delegated to him to reject unsatisfactory batches of medicinal products, and the name and function of the person to whom he is responsible. If ultimate responsibility for quality control is to be exercised by the holder of the product licence, this is to be stated.
(3) The name and address and degrees, diplomas or other qualifications of the person in charge of the animals referred to in paragraph 5(2) of this Schedule.
(4) The name and address and degrees, diplomas or other qualifications of the person to be responsible for the culture of any living tissue to be used in the manufacture of medicinal products.
8. An outline of the arrangements for the identification and storage of materials and ingredients before and during manufacture and for the storage of medicinal products after manufacture or assembly.
9. An outline of the arrangements at each of the premises where the licensee stores or proposes to store medicinal products for ensuring, so far as practicable, whether by maintaining records or other means, a satisfactory turn-over of stocks of medicinal products.
10. An outline of the arrangements—
(a)for maintaining production records,
(b)for maintaining records of analytical and other testing procedures applied in the course of manufacture or assembly for ensuring compliance of materials used in the manufacture of any medicinal products with the specification of such materials or medicinal products, and
(c)for keeping reference samples of materials used in the manufacture of any medicinal products and of the medicinal products.