Kymanox® Capabilities

The Kymanox Quality Control (QC) team provides knowledge and expertise to ensure that you align your practices to the revised European Union (EU) GMP Annex 1, a guidance document for the manufacture of sterile medicinal products.

What is EU GMP Annex 1?

EU GMP Annex 1 is a guidance document for the manufacture of sterile medicinal products that was recently revised and published on 25 August, 2022. Even if you currently do not have product approved by the EU, US FDA leaders have already indicated a desire to align with these standards. Adhering to Annex 1 requirements can help you improve product quality and reduce time and resources spent on remediating sterility and contamination-related issues.
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Kymanox Areas of Expertise

Kymanox has expertise in aseptic processing, microbiology, environmental monitoring, and contamination control, making us uniquely positioned to succeed in helping our clients adhere to the revised Annex 1 requirements for the manufacturing of sterile medicinal products. Kymanox can help carry out risk assessments, assess root cause behaviors, establish an effective Corrective and Preventive Action (CAPA) system, set-up investigation procedures, and update procedures in the case of arising issues.
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Contamination Control

Kymanox and our QC experts can help you identify and close gaps to align with the revised Annex 1 and ensure that your processes minimize contamination-related risk. We can help author a document to outline the necessary policies and procedures for contamination control, develop and implement training on the new guidelines of Annex 1, and help you implement smarter testing with documented risk-based sample plans that can improve efficiencies without sacrificing quality.
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Full Range of Services

Kymanox holds a 360° view of all quality monitoring services and supports these services with additional capabilities such as Quality Assurance, Auditing, CMC, Analytical Sciences, Regulatory Affairs, and more.
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Meet our Quality Control Experts

Jaime Rain, MMB

Markets That Benefit from Our Quality Control Solutions

Combination Products

Our experts understand the interaction between devices and drug products and are ready to support your next project


In the dynamic realm of biotechnology and cell and gene therapy we continue to offer innovation solutions and guidance


Drug development is constantly evolving with new regulations and technology, we stay up to date to maintain your compliance

Medical Devices

Building on over three decades of experience in the medical device industry, Kymanox has been at the forefront of innovation

The Kymanox Quality Control Difference

We ensure your Quality Control needs are not only right for your company but also aligned with regulatory expectations by blending our hands-on, practical quality control experience with other functional capabilities.
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"Right First Time” Execution

Our branded methodology, Ideal Knowledge TransferTM, combines technical project management, fundamental engineering practices, quality and regulatory expertise, and business acumen.
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Proven Broad Expertise

Our team of experts is focused on life sciences with extensive experience across drug and device development. No matter your challenge, we can help you conquer it.
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Flexibility & Agility

At Kymanox, we make it easy for clients to get the solutions they need, when they need it. Clients tell us our flexibility is one of the key reasons they keep coming back.
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