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This paper summarizes and draws up the decision tree for the in vitro consistency evaluation of oral solid generic drugs in combination with the relevant technical requirements such as “Requirements for Application Materials for Consistency Evaluation of the Quality and Efficacy of Oral Solid Preparations of Chemical Generic Drugs (Trial)”, and discusses the in vitro

This paper summarizes and draws up the decision tree for the in vitro consistency evaluation of oral solid generic drugs in combination with the relevant technical requirements such as “Requirements for Application Materials for Consistency Evaluation of the Quality and Efficacy of Oral Solid Preparations of Chemical Generic Drugs (Trial)”, and discusses the in vitro

In this article we will be dealing with Key Equipment And Technology For The Production Of Oral Solid Dosage Forms Batching Equipment   1.Automatic Batching Weighing System   Ingredients are an indispensable key link in the production of many solid dosage forms, and the accuracy of ingredients has an important impact on the quality of

Fluid bed granulation, also known as one-step granulation, is a method in which the three steps of mixing, granulation and drying of conventional wet granulation are completed in a closed container at one time. In 1959, Dr. Wurster from Wisconsin, USA first proposed fluid bed granulation technology, and then the technology developed rapidly and was

  With the expansion of Chinese APIs in the United States, Europe, Japan and other international markets, API manufacturers and R&D companies have increased the research and development of new drugs and generic drugs. After laboratory trials to large-scale production, large-scale pilot trials are required. Its purposes are: to verify the process conditions of the

The production workshop of the pharmaceutical factory is different from the general comfortable air-conditioned room. The indoor temperature and humidity control requires high precision. Generally, the temperature is required to be 22 °C ± 2 °C, the relative humidity is within 55% ± 5%, and the cleanliness of the air is required. There are also

After everyone understands the design requirements of the clean room, there is another link, which is the ventilation device of the laboratory. Some polluting gases must be removed to make the clean room achieve the required degree of cleanliness.   The pros and cons of a drug are not only directly reflected in the efficacy