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Senieer is a leading global Pharmaceutical Equipment Manufacturer And Supplier having different pharmaceutical equipment that are used in drug manufacturing most drugs are solid dosage forms here we have most of the information considering solid dosage forms. Solid Dosage form Solid dosage forms of drugs are drugs which are made with materials or which have features present in solid state. The most common […]

The research and development of an innovative drug needs to go through: disease market research, molecular mechanism research, target selection and confirmation, molecular design, synthesis and optimization of pilot compounds, pharmacodynamic pharmacokinesis and toxicity preliminary screening, preclinical research, clinical research, new drug review and listing, etc., from the establishment of new drugs to the final

1 Overview Of Cleaning Verification And Four Stages   In pharmaceutical enterprises, the same equipment may be used for the production of multiple products, and after the end of drug production, effective cleaning of the relevant equipment used in production is a necessary means to prevent drug contamination and cross-contamination. The provisions on cleaning and

This paper introduces several sterilization methods of sterile drugs : humid heat sterilization, dry heat sterilization, radiation sterilization, ethylene oxide sterilization and sterilization filtration, studies the sterilization principle, influencing factors, advantages and disadvantages of various sterilization methods, and products suitable for sterilization, etc., and selects the decision tree as the sterilization decision-making method of sterile

The application of biological clean rooms is becoming more and more extensive, and they are currently concentrated in hospital operating rooms and wards, pharmaceutical factories, biosafety laboratories, animal rooms, etc. The same level of clean room, due to different application areas, the requirements are also very different, the author tested a number of biological clean

Stages Of Development Of Generic Drugs   Oral Solid Preparations, Tablets   1. Chemical Properties, Production And Control In The Development Of Oral Solid Preparations   Through the analysis of the components within the packaging material of the control drug, the basic information about the control drug is obtained   (1) Prescription ingredients   (2)

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