Duties of inspectors

An inspector shall– (a) supervise the research, development, manufacture and trade of pharmaceuticals, as well as the medical organisation’s use of (b) not divulge technological, business and any other information gained from such (c) regularly promulgate the results of sampling examinations and inspections on the quality of 144 Food and Drugs (d) follow up on the inspections of any pharmaceutical manufacturer, pharmaceutical importer or pharmaceutical wholesaler, that the inspector has certified in conformity with relevant standards as established by the (e) not participate in manufacturing and trade, and shall not endorse or supervise the manufacture and sale of pharmaceuticals in the name of the inspector or that of any of his relatives; (f) receive operational guidance regarding the of any manufacturer, pharmaceutical importer or wholesaler and medical organisations from the competent authority; (g) supply a letter of confidentiality to the competent authority prior to his conduct of any inspections.