We share your passion for creating precise and accurate tools for clinical research. Let us help you get control, consistency, and flexibility over your assay oligo components.
You have an assay. We’ll help.
IDT’s expertise in GMP manufacturing allows us to help you through every step of your assay development, from discovery to commercialization. We offer a streamlined portfolio to aid in GMP service selection and order processing, with transparent pricing. When you are ready to move to GMP manufacturing, we offer control (change control, oligo master records) and consistency (lot-to-lot consistency and std or custom QC).
As you develop your molecular diagnostic or OEM assay, you need a strategic partner to help you meet your revenue goals with high-quality reagents, on-time delivery, and the ability to grow with you. With IDT, you can rely on:
IDT is your innovative expert with a broad product portfolio, tools that guide experimental design, expert technical support, and rapid turnaround times. You can count on:
Your product demand has grown, and now it is time to scale up with maximum efficiency. To do this, you will need an experienced collaborator who can provide scalability and manufacturing flexibility. IDT’s expertise will support this process through:
IDT puts quality first with:
IDT Strategic Services is an ally who can help manage all aspects of ordering and integration, with options to help you meet your budget, including:
DISCLIAMER: GMP refers to manufacturing under ISO 13485 standards.
For research use only. Not for use in diagnostic procedures. Unless otherwise agreed to in writing, IDT does not intend for these products to be used in clinical applications and does not warrant their fitness or suitability for any clinical diagnostic use. Purchaser is solely responsible for all decisions regarding the use of these products and any associated regulatory or legal obligations.