Quality Driven Approach

Guaranteed Quality with Aquabiliti

Uncompromised superior quality is first and foremost, the core foundation stone of Aquabiliti.

From innovative solutions to reliable products, we’re dedicated to exceeding industry standards and providing superior quality medical offerings.

Aquabiliti's team brings deep expertise in FDA-regulated medical device, SUS manufacturing, water for injection (WFI) generation and controlled environment filling. This knowledge enables us to not only produce high-quality bags but also deliver advanced packaging engineering solutions. We ensure optimal fit and functionality upon filling, minimizing issues such as creasing, inadequate support, and bag failure due to improper compatibility with drums.

With a long-standing commitment to SUS and rapid sterile product delivery, Aquabiliti offers customized solutions tailored to streamline your specific workflows. Every component used in our SUS manufacturing meets stringent standards, including biocompatibility (e.g., USP <88> Class VI), extractables and leachables (E&L), non-animal origin (NAO) materials, and endotoxin limits.

Trust Aquabiliti to provide reliable, high-quality solutions that enhance your manufacturing processes and ensure the safety and integrity of your products

Our Core Values

Graphic showing Aquabiliti's innovation in Single Use Systems for pharmaceutical and life science industries
Graphic showing Aquabiliti's commitment to client satisfaction when integrating Single Use systems for custom solutions
Graphic showing Aquabiliti's compliance with regulatory standards such as FDA and ISO

Quality Statement

Aquabiliti is dedicated to delivering the highest quality products to our clients by maintaining an effective quality management system that fulfills industry and regulatory standards.

To achieve this result Aquabiliti employees will:

  • Continuously improve and innovate safe and effective products

  • Ensure those products meet and exceed documented specifications and requirements

  • Enhance the quality system to conform at a minimum to meet 21 CFR Part 820

  • Establish quality objectives and strive everyday in achieving and surpassing those goals