pharmaceutical administration drug administration
1.The Japanese Pharmacopoeia (JP) was designated as the official Japanese drug standard by The Pharmaceutical Administration Law of Japan.
2.③Effects of serum containing drug on BEL7402 cells: HCC BEL7402 cells (introduced from Animal Experiment Center of Sun Yet-Sen University) were randomly assigned into 7 groups (10-well in each group): control group (added in RPMI-1640 medium in serum before drug administration with the 100 g/L serum final concentration), 5-FU group prepared with human serum RPMI-1640 medium containing 100 g/L concentration, 0.3, 0.6 and 0.9 mg/L final mass concentration 5-FU (Shanghai Xudong Haipu Pharmaceutical Company, Ltd, number 050106, 10 mL in each) and Chinese drug group (human serum was added with RPMI-1640 medium after taking drugs of 0.83, 1.67 and 2.50 mL/kg dose, 100 g/L serum final concentration).
3.Article 1 For the purpose of strengthening the administration of accredited supervisors and regulating their behaviors of on-the-spot supervision and inspection over drug production, these Provisions are formulated in accordance with the relevant provisions of the Pharmaceutical Management Law and other related provisions on drug manufacturing supervision and management.
