What are the procedures for the new Chinese medicine invented or developed by individuals in China to go on the market (enter clinical use)?

It is suggested to apply for a prescription patent before buying a patent. Prescription patents can be sold to pharmaceutical companies and hospitals. General hospitals don't buy it, and the main market is still in pharmaceutical factories.

It is impossible for an individual to convert a prescription into a drug. The reasons are as follows: it is impossible for an individual to have a GPM workshop to meet the production of finished drugs.

The steps to turn a traditional Chinese medicine prescription into a medicine are as follows: prescription (empirical prescription should summarize clinical data, classic prescription should have its source; Prove that the prescription is safe and effective) → pharmaceutical research (methods and control methods from medicinal materials to finished drugs: technology and standards) → pharmacological and toxicological research (efficacy, chronic toxicity, acute toxicity, pathology, etc. ) → Report to the US Food and Drug Administration → Obtain clinical approval → Clinical trials → Trial production → Report to the US Food and Drug Administration → Obtain production approval → Produce and go public. The whole process takes 3-5 years. And from the clinical trial, it must be the finished product produced by GPM workshop (produced by pharmaceutical manufacturers).