Medical devices and clinical lab equipment are expected to perform flawlessly from the moment they are unboxed. That level of reliability is only possible when every component, including the materials used in protective packaging, meets the same high standards. In today’s regulatory landscape, manufacturers are under increasing pressure to ensure their suppliers can support both product performance and compliance with evolving global regulations.
Choosing the right desiccant or oxygen scavenger is not just about controlling humidity or oxygen. It also means ensuring that these materials are produced under strict regulatory frameworks and are supported by thorough documentation and traceability.
Why Manufacturing Certifications Matter
Cilicant operates a dedicated cGMP-compliant manufacturing facility specifically built for healthcare and pharmaceutical-grade packaging materials. The facility is ISO 15378:2017 certified, meaning every production step, from sourcing to packaging, is aligned with international standards for medicinal packaging. This gives medical device manufacturers greater confidence in product quality and facilitates smoother market approvals worldwide.
In addition, Cilicant maintains an active Type III Drug Master File with the USFDA and supports Health Canada filings, allowing medical device and diagnostic kit manufacturers to integrate its desiccants and scavengers with confidence in regulatory acceptance.
Beyond Products: Technical Partnership
Cilicant’s strength lies not only in certification, but in its end-to-end capabilities. With in-house R&D, quality testing labs, and formulation flexibility, Cilicant works directly with manufacturers to co-develop protection systems that meet functional requirements and compliance expectations. This includes designing desiccants for seamless integration into devices and packaging lines, while maintaining full material documentation, lot traceability, and compliance with 21 CFR, RoHS, and HACCP.
Cilicant’s range offers silica gel and molecular sieve desiccants in tablet, sachet, and reel formats, each engineered to meet stability requirements across a wide variety of applications.
Meet us at ADLM 2025
For engineers, lab managers, and compliance teams, regulatory readiness starts with the right materials.
Visit Cilicant at Booth #3438 at ADLM 2025 in Chicago to learn how our desiccant technologies can support your product’s safety, stability, and global acceptance.
Choosing the right desiccant or oxygen scavenger is not just about controlling humidity or oxygen. It also means ensuring that these materials are produced under strict regulatory frameworks and are supported by thorough documentation and traceability.
Why Manufacturing Certifications Matter
Cilicant operates a dedicated cGMP-compliant manufacturing facility specifically built for healthcare and pharmaceutical-grade packaging materials. The facility is ISO 15378:2017 certified, meaning every production step, from sourcing to packaging, is aligned with international standards for medicinal packaging. This gives medical device manufacturers greater confidence in product quality and facilitates smoother market approvals worldwide.
In addition, Cilicant maintains an active Type III Drug Master File with the USFDA and supports Health Canada filings, allowing medical device and diagnostic kit manufacturers to integrate its desiccants and scavengers with confidence in regulatory acceptance.
Beyond Products: Technical Partnership
Cilicant’s strength lies not only in certification, but in its end-to-end capabilities. With in-house R&D, quality testing labs, and formulation flexibility, Cilicant works directly with manufacturers to co-develop protection systems that meet functional requirements and compliance expectations. This includes designing desiccants for seamless integration into devices and packaging lines, while maintaining full material documentation, lot traceability, and compliance with 21 CFR, RoHS, and HACCP.
Cilicant’s range offers silica gel and molecular sieve desiccants in tablet, sachet, and reel formats, each engineered to meet stability requirements across a wide variety of applications.
Meet us at ADLM 2025
For engineers, lab managers, and compliance teams, regulatory readiness starts with the right materials.
Visit Cilicant at Booth #3438 at ADLM 2025 in Chicago to learn how our desiccant technologies can support your product’s safety, stability, and global acceptance.
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