CRISPR cGMP gRNA Manufacturing

For customers looking to accelerate their CRISPR genome editing program from discovery to clinical trials, our Engineering Run and full cGMP guide RNA manufacturing services offer a streamlined and regulatory-compliant solution. Backed by comprehensive documentation, our guide RNAs simplify regulatory filings, offering a straightforward path to clinical success.

Lab to life changing advances. We’ll help.

OVERVIEW

IDT is a global leader in CRISPR genome editing with a complete workflow from design to analysis. Our CRISPR product portfolio includes a comprehensive set of tools, reagents, and services for all your genome editing needs, including discovery, preclinical research, and clinical applications. As your trusted partner, we're committed to providing you with the highest quality products and services to help accelerate your research and bring your discoveries to life.

• Proven excellence: For more than 35 years, IDT has been enabling genomic research with an oligonucleotide manufacturing process unlike anyone else in the industry. Our expertise ensures a reliable partner in your journey from research to clinical applications.
• State-of-the-Art facility: Experience the benefits of our 41,000 square foot Therapeutic Oligonucleotide Manufacturing Facility designed to provide the CRISPR cGMP guide RNA manufacturing grades to align with your development path, supporting you from preclinical studies to clinical trials.
• Comprehensive quality control: We prioritize quality with thorough Quality Control (QC) and analytical testing. Each CRISPR guide RNA meets the highest standards of quality and consistency.
• Regulatory support aligned to clinical phases: IDT is prepared to support you with required information tailored to your unique needs, based on use, clinical program phase, and modality. Navigate regulatory requirements with confidence.
• Dedicated expert team: Your project is in the hands of a dedicated, cross-functional team of professionals at IDT. Each team member is an expert in their field, working diligently to ensure the success of your CRISPR therapeutics program.

Request a consultation

Start the conversation today to explore how our cGMP manufacturing service can accelerate your CRISPR therapeutics project. Click on "request a consultation" to provide brief information about your project, and we'll be in touch to discuss it ASAP.

REQUEST A CONSULTATION