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  Purpose    Taking the recovery rate as the entry point, the relevant concepts and practices of the cleaning residue analysis method in the cleaning verification of drugs are studied, which provides a reference for the research of residue analysis methods for pharmaceutical...

More and more people are getting better and better treatment through drugs and medical devices – 50 drugs were approved in the US market alone in 2021, continuing the positive growth trend of recent years. However, compared with the achievements and commercial potential of pharmaceutical...

Clean workshop, also known as clean room, dust-free workshop, clean room, etc. Clean workshop in pharmaceutical and biological engineering, precision machinery, medical and health, food, electronic materials and other fields of application is very extensive. In FED-STD-2, a cleanroom...

On September 24, 2021, the latest issue of Drug Discovery Today magazine recently published a paper entitled R & D efficiency of leading pharmaceutical companies-a 20-year analysis, analyzed the R & D data of 14 leading global drug R & D enterprises, and revealed some...

There are currently three main types of fluid bed processes: top spray, bottom spray, and rotary tangential spray. Due to the different equipment construction, the material fluidization state is also different. Coating quality and formulation release characteristics may vary with...

Recently, Nature’s sub-journal “Nature Review Drug Discovery” and biopharmaceutical industry media Evaluate Vantage both published articles to analyze and predict the top 10 global drug sales in 2022. Coincidentally, two analysis articles gave the same prediction....

  There are a number of energy savings in cleanrooms such as heating, ventilation and air conditioning (HVAC), process cooling, compressed air, and a few others. Below are ten tips for new and existing plants to provide energy efficiency solutions that provide reliable technology...

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...

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...

01 Drug Development Process, Chemical Characterization, Production And Control In Oral Solid Dosage Forms   Components in the formulation BE information 02 Chemical Characterization, Production And Control In Oral Solid Dosage Forms   Reverse Engineering incluation of three different...