Avioq is an in vitro diagnostic medical device manufacturer and a contract development, contract manufacturing organization.

Based in Research Triangle Park, North Carolina Avioq has a FDA licensed manufacturing facility and large, modern R&D laboratories.

Our products include an FDA licensed HTLV-I/II assay for screening serum and plasma from blood donor and cadaveric samples, which also has CE marking and Health Canada approval.

The Avioq HIV-1 assay is the only product with FDA approved claims for testing serum, plasma, dried blood spots, and oral fluid specimens.

The FDA approved HIV Profile™ assay is an enzyme-linked immunosorbent assay (ELISA) for confirmation and differentiation of individual antibodies directed to various gene products of HIV-1 (Group M & Group O) and HIV-2 in human serum or plasma. It is intended as an additional, more specific test to confirm the presence of antibodies in specimens repeatedly reactive in diagnostic procedures.

Why work with Avioq for your next CDMO project?

Instead of using consultants who talk about the regulatory process we actually live it. We develop and manufacture our own FDA and CE Mark products to the highest standards.

The manufacturing facility is FDA (BLA) licensed and ISO 13485:2106 certified. The facility has been inspected numerous times by FDA and ISO, as well as by external partners.

Need a quick answer? We can help you with:

    ● Exploratory research
    ● Proof of concept projects
    ● Feasibility studies
    ● Research lots

If you entrust your project to Avioq, we will focus on getting your product through our mature Quality System, approvable by Regulatory Authorities, manufactured and to market as quickly as possible. Our team will guide you past the regulatory delays and pitfalls.

Our R&D, quality and manufacturing teams have successfully designed and developed numerous medical diagnostic products during the past 25 years.

Life Sciences

Manufacturing

Medical Devices

Avioq

Avioq's headquarters in Research Triangle Park, NC, United States

Cham Chetty

Craig Carson

Mike Cronin

This department oversees the entire manufacturing process and ensures efficient tech transfer and project management.

Manufacturing Operations

This department is responsible for ensuring that products meet quality standards through testing and evaluation processes.

Quality Assurance

This department focuses on promoting and selling products or services while managing relationships with customers.

Sales and Marketing

The Business Development team at Avioq is responsible for identifying and securing new business opportunities and partnerships that align with the company's strengths in in vitro diagnostic medical device manufacturing and contract development. Their tasks include market research, strategic planning, client relationship management, and negotiating contracts. This team works to expand Avioq's market presence, foster collaborations, and ensure sustained company growth by leveraging the company's FDA-licensed manufacturing facility and extensive R&D capabilities.

Business Development

The Research and Development (R&D) team at Avioq, based in Research Triangle Park, North Carolina, focuses on the innovation and development of cutting-edge in vitro diagnostic medical devices. This team engages in exploratory research, proof of concept projects, feasibility studies, and the production of research lots. They drive the development of proprietary FDA-approved assays for HIV and HTLV screening, ensuring compliance with stringent regulatory standards. Through their expertise, they guide CDMO projects from concept to market, effectively navigating the regulatory landscape to deliver high-quality diagnostic products.

Avioq

Org chart

Teams

Manufacturing Operations

Quality Assurance

Sales and Marketing

Business Development

Research and Development

Offices

Avioq

Org chart

Teams

Manufacturing Operations

Quality Assurance

Sales and Marketing

Business Development

Research and Development

Offices

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