List of Pharmaceutical and food related products
- classification：Pharmaceutical and food related
4906～4920 item / All 33352 items
Reduce the workload from handling heavy objects! Here are five case studies that solved customer challenges! We are also accepting free consultations and tests tailored to your work!
- Other conveying machines
Support from product planning to filling, processing, and shipping for additives, cleaning agents, chemicals, deodorizing and disinfecting agents, etc.! For those who have raw materials but no place t...
- Other consumables
- Processing Contract
Insufficient cleaning of the kettle with 'solvent cleaning' is resolved with 'decomposition cleaning'! Thoroughly prevent contamination and provide high-quality dissolution contracting starting from 5...
- OEM
- OEM Manufacturing Services
We accept solvent cuts of solid resin starting from 50L! We prevent contamination through decomposition cleaning and can flexibly process high-viscosity and difficult-to-dissolve materials. We also ac...
- OEM
- OEM Manufacturing Services
We accept orders for 50L of release and cleaning solution for molded products! We maintain quality with decomposition cleaning and can flexibly process difficult-to-dissolve items. Small lot and spot ...
- OEM
- OEM Manufacturing Services
Thoroughly eliminate contamination during the dissolution processing! With double measures of decomposition cleaning and precision filtration, we offer contract manufacturing of high-purity products s...
- OEM
- OEM Manufacturing Services
Ease of securing workers familiar with medical logistics! BCP response through the installation of emergency generators.
- Other quality control systems
Quality changes with dispersion. Pre-validation of the reproducibility of resin materials through testing.
- Emulsifier/Disperser
- Vacuum degassing machine
- Dispersion/emulsification equipment/homogenizer
What are the reasons for changes in results from the lab to mass production? Causes and countermeasures for the deterioration of distributed quality during scale-up.
Despite obtaining good dispersion results in the lab, the challenge of unstable quality upon mass production occurs in many settings. The main cause of this is that the dispersion conditions are not replicated due to differences in scale. In lab equipment, the smaller size leads to higher energy density, making shear and flow more uniform, while in mass production equipment, the larger scale often results in insufficient dispersion energy at the same rotational speed and processing time. Additionally, differences in equipment structure and flow patterns can cause variations in the shear history and residence time experienced by particles, leading to differences in the dispersion state. Furthermore, simple scale-up does not ensure that critical parameters such as flow rate, residence time, and shear intensity match, making it difficult to reproduce the same results as in the lab. To address these challenges, it is essential to focus on process design based on dispersion energy density and flow conditions rather than merely increasing equipment size. By designing the system so that particles pass through the processing area under consistent conditions, it is possible to achieve reproducible dispersion quality even when the scale changes, as seen in inline continuous processing.
The strength is determined by the variance. Visualize quality variations through testing before mass production.
- Emulsifier/Disperser
- Vacuum degassing machine
- Dispersion/emulsification equipment/homogenizer
What are the reasons for changes in results from the lab to mass production? Causes and countermeasures for the deterioration of distributed quality during scale-up.
Despite obtaining good dispersion results in the lab, the challenge of unstable quality upon mass production occurs in many settings. The main cause of this is that the dispersion conditions are not replicated due to differences in scale. In lab equipment, the smaller size leads to higher energy density, making shear and flow more uniform, while in mass production equipment, the larger scale often results in insufficient dispersion energy at the same rotational speed and processing time. Additionally, differences in equipment structure and flow patterns can cause variations in the shear history and residence time experienced by particles, leading to differences in the dispersion state. Furthermore, simple scale-up does not ensure that critical parameters such as flow rate, residence time, and shear intensity match, making it difficult to reproduce the same results as in the lab. To address these challenges, it is essential to focus on process design based on dispersion energy density and flow conditions rather than merely increasing equipment size. By designing the system so that particles pass through the processing area under consistent conditions, it is possible to achieve reproducible dispersion quality even when the scale changes, as seen in inline continuous processing.
Resolve issues of not dissolving and clumping in advance. Test the dispersibility of the protein.
- Emulsifier/Disperser
- Vacuum degassing machine
- Dispersion/emulsification equipment/homogenizer
What are the reasons for changes in results from the lab to mass production? Causes and countermeasures for the deterioration of distributed quality during scale-up.
Despite obtaining good dispersion results in the lab, the challenge of unstable quality upon mass production occurs in many settings. The main cause of this is that the dispersion conditions are not replicated due to differences in scale. In lab equipment, the smaller size leads to higher energy density, making shear and flow more uniform, while in mass production equipment, the larger scale often results in insufficient dispersion energy at the same rotational speed and processing time. Additionally, differences in equipment structure and flow patterns can cause variations in the shear history and residence time experienced by particles, leading to differences in the dispersion state. Furthermore, simple scale-up does not ensure that critical parameters such as flow rate, residence time, and shear intensity match, making it difficult to reproduce the same results as in the lab. To address these challenges, it is essential to focus on process design based on dispersion energy density and flow conditions rather than merely increasing equipment size. By designing the system so that particles pass through the processing area under consistent conditions, it is possible to achieve reproducible dispersion quality even when the scale changes, as seen in inline continuous processing.
From October 29 (Tuesday) to 31 (Thursday), 2024! We will be exhibiting small ultrasonic dispersion devices and ultrasonic generators!
- Emulsifier/Disperser
- Powder Supply Device
- Dispersion/emulsification equipment/homogenizer
What is decentralized process design? Key points for stabilizing quality.
In dispersion engineering, stable quality cannot be achieved solely based on the performance of the equipment. What is important is the overall design of the process, taking into account material properties and process conditions. This is referred to as dispersion process design. Dispersion quality is determined not only by the strength of shear but also by multiple factors such as flow state, residence time, and method of input. If these conditions are not properly designed, localized agglomeration or variation can occur, making it difficult to maintain stable quality. For example, poor wetting during powder input or the occurrence of stagnant areas due to flow bias can lead to clumping or dispersion issues. Additionally, even if the shear energy is sufficient, if it does not act uniformly on all particles, differences in dispersion state will arise. Therefore, in dispersion processes, it is crucial to design "flow," "shear," and "processing time" as an integrated system. This allows for all particles to receive the same dispersion history, achieving uniform and highly reproducible dispersion quality. In particular, inline continuous processing has the advantage of maintaining consistent conditions within the flow, making it easier to ensure reproducibility in process design. Dispersion process design is a key concept for stabilizing quality and successfully scaling up.
![[Catalog Presentation] High-Pharmac...](https://image.mono.ipros.com/public/product/image/2080829/IPROS18174704042808786662.png?w=280&h=280){kind=small}
Exhibition of local exhaust dust collection devices specialized for highly active substances, automatic dispensing systems for single-use bags, and various consultations for the construction of pharma...
- Other dust collectors and related products
Increased absorption rate with the latest liposome technology!
- Food ingredients (powder)
Liposome NMN using high-safety sunflower lecithin × plant sterols (derived from pine).
- Food ingredients (powder)
Overcoming the traditional weakness of NAD+ regarding "low absorption rate" with unique liposome technology.
- Food ingredients (powder)
Unique liposome technology that delivers NAD+ "as is."
- Food ingredients (powder)
22-inch widescreen LCD touchscreen PC operable in Zone 2
- Touch Panel
- Industrial PCs
- FPD/Touch Panel