Regulation 17 Amendment of the Medicines (Applications for Grant of Product Licences—Products for Human Use) Regulations 1993

in paragraph (2) of regulation 1 (citation, commencement and interpretation), after the definition of “expert” there shall be inserted the following definition—

• ““principles of good laboratory practice” has the same meaning as in the Good Laboratory Practice Regulations 1997;”; and

in paragraph 17 of Schedule 1 (information, documents, samples and other material required in respect of applications), the words “referred to in that sub-paragraph” shall be omitted.