Industries and Solutions
Pharmaceutical
Release time:
2020-03-05 11:04
solution
The product options that Shunzi Machinery can provide for the pharmaceutical industry include the ecodos and ecoflow series pumps of hygienic design and the mechatronic drive unit independently developed by Shunzi Machinery. These products can meet the various highest-level requirements of the pharmaceutical industry.
High dose accuracy
For precise reproducibility of continuous processing flow
Wide measurement range
Suitable for different media
The completely leak-free overflow cavity saves products and protects the environment
Short product residence time and soft transmission
Depending on the options: CIP and SIP (online cleaning and disinfection capabilities)
Hygiene and pharmaceutical design
Comply with FDA (U.S. Food and Drug Administration) material specifications
3.1 Material certification
EHEDG test certification, QHD certification
Meet the requirements of clean room installation
Shunzi mechanical metering system has advantages in fast and highly accurate flow control.
The Shunzi Mechanical Metering System can not only monitor pumps and flow meters in accordance with the performance curves stored in the control system, but also monitor their authenticity in real time. This ensures high operational reliability and metering accuracy.
Another advantage is that the entire production process can be recorded without any omissions according to the technical requirements of the pharmaceutical industry. In the process of selecting the appropriate flowmeter and other components, Shunzi Machinery can provide a lot of practical experience: to ensure that all components are matched with each other, so as to ensure that the entire metering system has perfect performance.
Background note
Flow Description
In the pharmaceutical processing process, the medium must be added and mixed. This may also mean that the system must first prepare the products to be delivered (such as mixing, salt melting, temperature control, ingredients, etc.). Therefore, a customized solution will require the functions of the system and the adjustment of individual components in the entire system.
In fact, the transmission of the medium must be carried out under certain process conditions, such as certain pressure and temperature conditions, process control, and high requirements for the entire system solution.
For a stable processing flow, coordinated and professionally programmed instrumentation and control systems and technologies must be adopted. The use of storable formulas in the system control makes the processing flow reliable and has the greatest degree of reproducibility. Recording of the process and results is essential for stable production and meeting cGMP (Dynamic Good Manufacturing Practice) requirements.
Different user levels have corresponding permissions, and the design concept of the system guarantees permissions and validity confirmation, so that the CFR21 Part 11 specification can be realized.
The system products must comply with the special quality specifications of the pharmaceutical industry and can be verified at any time.
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