The ETO Sterilizer market in Australia and New Zealand is expected to experience significant growth over the next several years. This is due to the rise in the number of hospital and medical centres. These facilities will require sterilization in order to reduce their risk of infection. In addition, the demand for sterilizers will increase due to the aging population and increasing life expectancy. As a result, this will create new opportunities for manufacturers of ETO sterilizers.
Why is Australian and New Zealand ETO Sterilizer Market Growing?
The Australian and New Zealand ETO sterilizer market is expected to witness significant growth in the upcoming years. This is due to the rising need for sterilising services, especially in the countries in the Asia Pacific region. In addition, the rising number of healthcare employees is also expected to increase the demand for these services.
The demand for sterilization services will be driven by an increasing number of hospital admissions. Moreover, technological advancements are expected to drive segment growth. These include advances in instrument capabilities, low-temperature sterilization systems, and greater material compatibility. Increasing product launches are also expected to boost the segment’s growth.
Surgical operations are expected to account for a major share of the overall end user market. Moreover, the growing awareness about cleanliness and sanitary conditions is expected to drive the demand for sterilisation services. Moreover, the rising prevalence of hospital-acquired infections (HAIs) and the need to keep the environment clean are expected to fuel the growth of the segment.
Healthcare reforms and the introduction of new medical devices are also expected to offer high-growth opportunities to the market.
Hence, the global market for sterilization services is expected to expand at a CAGR of 5.1% from 2023 to 2030. Despite the significant market size, there are opportunities for market players to thrive.
What is the Segmentation of the Australian and New Zealand ETO Sterilizer market?
ETO Sterilizers are a type of sterilization technique, which is widely used. It is a low temperature gaseous process that is commonly used in healthcare facilities.
The sterilization equipment industry is a global market. It is divided into pharmaceutical, biotechnology, and medical device companies. In addition, it is also categorized into other end users.
The Australian and New Zealand market for sterilization services is expected to grow at a robust rate in the coming years. The rising number of surgical operations and hospital admissions is expected to boost demand for sterilization services. Increasing medical tourism is also contributing to the growth of the market.
The growth of the market can be attributed to various factors such as the rise in geriatric population, the increased number of hospitals, and the growing pharmaceutical and medical devices industries.
In addition, the increasing demand for reusable medical devices and equipments is also expected to drive the growth of the sterilization services market. Hospitals are also expected to have a significant share of the end-user market.
Several sterilization services providers are also expanding their business in underserved communities to reach new and potential markets. They are also partnering with academic institutions to help them gain more experience and knowledge. This will enable them to stay competitive and to expand into new markets of Australian and New Zealand.
As a result, the global contract sterilization market is expected to experience steady growth over the next five years. This is due to several factors, such as technological advancements and cost-effective products. Moreover, the need to upgrade and provide customized services is expected to increase the market.
Validation Requirements for Ethylene Oxide Sterilization
The validation of ethylene oxide sterilizer is a critical part of the manufacturing process. It’s important to perform these tests on new equipment or when there are changes to existing processes. Failure to follow these procedures can lead to delays in the production cycle, which could cost the business more money.
Several methods can be used to validate ethylene oxide sterilization. These include comparative resistance testing and a microbial challenge. Choosing the best method for your application is an important step.
In most cases, comparative resistance testing should be performed before a validation cycle. This is particularly true for the overkill method. A microbial challenge can be generated by inoculating a simulated product with a certified inoculum.
During a validation cycle, the chamber and product load temperature should be monitored. In addition, humidity levels should be tested. If these measures are not able to withstand the EtO gas sterilization process, then the device may need to be revalidated.
If a microbial challenge is not available, a biological indicator (BI) can be placed around the product. BIs can reduce the exposure of the sterilant to the patient or clinician.
Once the EO sterilization process is complete, the BI should be stored in a location where it will not be exposed to the sterilant. Sterilization is never completely effective and there will always be a chance of non-sterile products in a batch.
Depending on the type of microbial challenge and the type of EtO sterilization, the BI can be simulated or inserted into culture media. For a biological indicator, the culture medium will promote the growth of biological indicators.
To validate a new EO sterilization cycle, it’s important to have several cycles run. Each cycle should have a different graded time exposure to EO.
The Bottom Line
A number of reliable studies have been conducted on the topic. It is not a secret that Australia and New Zealand are medically inclined countries and the need for quality health care is ever increasing. The competition in the private sector is stiffer than that in the public domain. Also, ETO based sterilisation is an effective way to reduce cross infection.
