(a) All types of records and record books should be kept properly,

(b) Necessary number of staff should be kept for work related to production or analysis,

(c) If any kind of loss or adverse effect is known or received from the consumption of the produced medicine, the manufacturer should review the quality and production process of the medicine and immediately take necessary precautions, (d) returned or the recalled medicines should be properly tested, analyzed and evaluated in order to be reprocessed and put on sale-distribution. and

(f) must use the tools or machines prescribed by the department for making drugs that do not fall under the above-mentioned class division or of other formulations.