The team at Steripack Ireland is acutely aware that our products play a crucial role in enhancing the quality of patient’s lives. Through the use of sterile barrier packaging, we prevent contamination and maintain sterility, thereby mitigating the risk of infections and other complications. This ultimately leads to an overall improvement in the quality of life for everyone, including our families, friends, and neighbours.
At Steripack Ireland, each and every employee bears the responsibility of ensuring quality.
We are unwavering in our commitment to creating an environment where processes, technologies and tools are optimally utilized towards this end.
Our priority at Steripack Ireland is to get things right the first time, which is why we adhere to various ISO standards, including ISO 13485:2016 and requirements for packaging of medical devices ISO 11607-2019. This standard specifies the requirements for a quality management system for medical devices. To ensure compliance with regulations, drive consistency and reduce risk, we have established stringent quality standards.
Creative solutions are necessary to tackle complex challenges.
We have a highly skilled workforce equipped with extensive expertise and process competencies.
Whatever your needs may be, we are poised and ready to provide assistance.
Steripack Ireland have a company-wide continuous improvement program in place that drives our systems and we constantly explore novel approaches to enhance the quality of service we deliver to our clients.
Our unwavering focus on putting our clients first remains a top priority.
We have in-depth understanding of country specific requirements. This means that Steripack Ireland can guarantee
solutions that are tailored to the needs of local markets and adhere to international standards.