Let's discuss your cGMP guide RNA needs for your CRISPR therapeutic development

Our cGMP manufacturing service is tailored to seamlessly take your project from the discovery phase to clinical trials, ensuring precision, reliability, and compliance at every step. To further support regulatory compliance, IDT offers gRNA sequencing services for customers manufacturing their CGMP gRNAs with us.

How we can help you:

1. Project consultation: Initiate the conversation by sharing your project details. Our team will review your requirements and provide tailored recommendations to optimize your CRISPR guide RNA manufacturing process and advise on quality control assays, including gRNA sequencing.
2. Custom manufacturing solutions: Whether you need small-scale batches for pre-clinical or large-scale production for clinical trials, we offer flexible manufacturing solutions to suit your project's unique needs.
3. Quality assurance: Ensuring the highest quality is our priority. In addition to rigorous QC and analytical testing, IDT offers complete NGS-based gRNA sequencing to identify sequence variants.
4. Regulatory compliance: Navigating the regulatory landscape is complex. Trust our expertise in cGMP compliance to ensure that your CRISPR guide RNAs meet the necessary regulatory standards for clinical trials.

Let's take your CRISPR therapeutics research into the clinic!

Start the conversation today to explore how our cGMP manufacturing service can accelerate your CRISPR therapeutics project.

Rapidly move from the lab to therapeutic clinical trials. We'll help.