In recent years, with the continuous development of science and technology, the development of domestic testing instruments has attracted more attention. Its application in the pharmaceutical industry is also increasingly widespread. However, how to accelerate the transformation and upgrading of medical testing instruments from "Made in China" to "Created in China" still has many practical difficulties that need to be overcome.
In the medical instrumentation industry, innovations have been plagued by various factors for R&D, production, market circulation, and application links. This has led to a hopeful but helpless development of detection instruments.
The testing equipment developed and produced in China has reached the international level in the mid-1990s, but the high-end demand mainly depends on imports. The impression made by domestic equipment to general users is poor product reliability, low precision, and low level of technology.
Poor quality of the testing equipment is a very complex cause. The main points are as follows:
1, product design and development is not in place, process documentation is not perfect;
2. There is no well-established industrial industry chain;
3. The internal quality assurance system is not perfect;
China's inspection instrument industry is uneven and the overall quality system is imperfect. This status will inevitably damage the image and brand of the entire industry. Based on the instrument industry's own characteristics of multi-category and small-batch, it is very cumbersome and complex to solve the problem of low product quality. This difficult and difficult process requires a good attitude to support.
Therefore, domestic testing equipment manufacturers must have the concept of long-term investment, and the production of sophisticated products is the company's highest goal, not only to solve the problem of cost-effective, but also should improve after-sales service.
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