How to be a qualified pharmaceutical manufacturer under the guidance of GMp

You should have professional business knowledge and ability to do your job. First of all, you should have general professional knowledge and management ability, that is, you should have the same level of knowledge and ability as the custodian. Such as the formulation of rules and regulations of each room, the correct storage of instruments and drugs, the recording of account books, the formation of files and so on.

Managers must be proficient in the teaching content of related disciplines, know the environment required for each drug like the back of their hands, and know the specifications, models and performance of all drugs like the back of their hands. To master this knowledge, they should also have people who can independently complete all kinds of management, sum up experiences and lessons, and communicate with various departments.

The most important and basic ability is the ability to strengthen management, eliminate hidden dangers and avoid any accidents during the whole operation of drugs.

The mission of pharmaceutical manufacturers: to ensure the safety, effectiveness, uniformity and stability of drugs.

First, social propaganda. The biological endowment of human beings has been urging human beings to improve their health and prolong their life as much as possible to ensure human reproduction. Drugs have attracted much attention because of their special effects. In modern society, the right to health and the right to life have become basic human rights protected by law. Therefore, drugs are related to the reproduction and development of the whole human society. The public announcement of drugs is the basis of establishing universal medical care and medical insurance system.

Second, the duality of roles. Drugs can prevent and treat diseases and restore and protect health. However, drugs are toxic in three aspects, and any drug has different degrees of toxic and side effects. Therefore, drugs can save lives and protect health as long as they are properly managed and used. On the contrary, it will degenerate into a terrible poison, endangering human health and life safety.

Third, the oneness of quality. The physical, chemical, biopharmaceutical, safety, effectiveness, stability, uniformity and other quality indicators of drugs must meet the standards prescribed by the state. Only drugs that meet the national standards can guarantee the curative effect. If it is lower than or higher than the specified quality standard, it may reduce or even lose the curative effect of the drug or aggravate the toxic and side effects of the drug. Therefore, only qualified drugs are allowed to enter the circulation channel, and defective or unqualified products are absolutely not allowed.

Biological drugs refer to a kind of products that are used for prevention, treatment and diagnosis by using the research results of microbiology, biology, medicine and biochemistry. From organisms, biological tissues, cells, organs, body fluids, etc. Comprehensive application of scientific principles and methods such as microbiology, chemistry, biochemistry, biotechnology and pharmacy.

Biopharmaceutical raw materials are mainly natural biological materials, including microorganisms, human bodies, animals, plants, marine life and so on.