In these Regulations, unless the subject or the context otherwise requires,–
(a) "Act" means the Medicines Act, 2035.
(b) "Department" means the Drug Administration Department.
(c) "Manager" means the head of the department.
(d) "Inspector" means an inspector having qualifications as per Section 23 of the Act.
(e) "Analyst" means a person appointed by the department from among the persons who are working on drug analysis in a laboratory, laboratory, hospital, dispensary or clinic having the qualifications as per Section 23 of the Act.