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From the cutting-edge industry trends, technological innovations, to product introduction and case studies, Senieer® offers comprehensive understanding on pharmaceutical industry for you.
The Basic Idea Of Research On The Source And Attribution Of Impurities In Compound Preparations Of Chemical Medicines
In the impurity research work of compound preparations, it is necessary to adopt appropriate methods to analyze and determine the source of each impurity, conduct qualitative research and attribute it, because the determination of the impurity limit must be based on a clear attribute....
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Analysis On Cleaning Validation Problems In Inspection Of Pharmaceutical Enterprises
Part 1 worst Condition   Theoretically, the different equipment involved in each variety should have its own cleaning operation procedures confirmed. However, in the practice of drug production, it is impossible and unnecessary for enterprises to spend manpower, material resources,...
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How To Choose A Suitable WIP Or CIP Sieve Machine?
Leakage of highly active drugs will seriously endanger the safety of operators – therefore, as more and more highly active compounds are approved as new drugs, pharmaceutical companies have more and more requirements for the closed production of tablet drugs . Drugs of OEB 3...
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Analysis On The Application Of Quality Risk Management In Drug Storage
Enterprises should take effective quality control measures in drug storage and other links to ensure drug quality. Enterprises should adopt a forward-looking or retrospective approach to assess, control, communicate and review the quality risks in the drug circulation process [1]....
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How To Produce Biopharmaceuticals Through Single-Use Continuous Production And Process Intensification
The high cost of medicines has repeatedly become a major bottleneck in the healthcare industry as large populations cannot afford prescription treatments. At the molecular level, many innovations are underway, including various recombinant monoclonal antibodies (mABs), antibody drug...
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The Issue Of Tablet Capping And Its Resolution
  The Issue Of Tablet Capping And Its Resolution   In tablet formulation, the term “capping” refers to a tablet failure break that happens soon after compression during the breakage force .   Capping is a manufacturing error that should be caught at the...
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Defective Color Variation In Coated Tablets
  Defective Color Variation in Coated Tablets The collection of tablet coating faults is comprehensive, encompassing a wide range of flaws seen during the practical application of the coating process.   This article will go over a very typical tablet coating problem that...
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Lifting Columns For Pharmaceuticals
Lifting Columns For Pharmaceuticals   The excellent design, sturdy construction, and electromechanical lifting motor of Senieer’s pharmaceutical lifting columns set them apart.   Pharmaceutical Lifting Columns with Linked Electro – mechanical Elements that Save...
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What Is The Importance Of Cleaning Validation In Pharmaceutical Manufacturing?
Pharmaceutical production is a practice that necessitates a high degree of hygiene and uniformity in order to ensure the safety of the output. One part of this procedure is clean validation, which guarantees that the machinery and procedures stay completely free of pollutants.  ...
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What Should We Do If The Edge Of The Tablet Is Knocked During Coating?
Film coating technology is to use a certain process to coat a coating material on the surface of the drug, which can play various functions such as beautification, protection and control of the drug effect as expected. This technology can overcome the shortcomings of many medicines,...
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