(1) The suppliers who purchase main raw materials and packaging materials are relatively fixed, and the quality evaluation of suppliers is adhered to.
⑵ The plant area is planned according to the principle of function and pollution prevention.
⑶ Workshop production requires reasonable layout, avoiding pollution and cross-contamination, and meeting the specified cleanliness requirements.
(4) Rational allocation of pharmaceutical equipment, using advanced equipment and intelligent equipment as far as possible, and eliminating equipment and facilities that are easy to cause pollution and cross-contamination in production.
5] All work is recorded. Really make documents the "law" of enterprises, and oppose copying, hard copying, execution of documents as a form or display of documents.
[6] Standardize various operations.
Once strict quality management requirements. Implement a three-level quality management system, improve the quality evaluation system, supervision system and reporting system, and constantly improve the level of drug standards.
The scientific nature of verification.
(9) Institutionalization of personnel training.
⑽ Regularization of health work.
⑾ Improve after-sales service, report major quality accidents and adverse reactions of drugs in time, so that the quality of drugs is under strict supervision and control, and nip in the bud.