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QA/QC Specialist
Crucial to every molecular diagnostic or OEM assay is a certified partner that will ensure your product meets all regulatory and quality requirements during development and commercialization.
Our Quality Assurance and B2B account manager teams are here to assist you during your verification and validation phase. We share your passion and commitment for better healthcare outcomes, which is why our custom solutions have been repeatedly trusted to create fast, sensitive, and accurate molecular tools for improved disease research and clinical diagnostics.
You have an assay. Let’s build it together.
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Request a consultation with one of our experts!
What you get with an IDT partnership:
- ISO 13485 and ISO 14644 certifications
- US FDA registration (Registration 3004513294)
- Traceability to support your customers—LIMS batch history record for every GMP oligo, Change Control Notification (CCN) service, including right to approve
- >35 successful audits per year
Learn how IDT can help your team
Learn how we help your team through every phase, from discovery to commercialization.
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B2B Capabilities Flyer
Learn how partnering with IDT can give your team everything it needs to successfully transition from discovery to commercialization.
Partnering with IDT
Get information on working with our dedicated B2B team, and details on forms and timelines.
Learn moreRUO or GMP oligos?
Important considerations when commercializing molecular assays for IVD applications
Learn moreStrategic Collaborations
We’ve partnered with Argonaut MS, Clear Labs, Roche, and Illumina to increase our capabilities and co-develop assays for multiplex PCR, NGS, and more.
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