In-vitro Diagnostic Regulation is here

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Are you ready for IVDR?

The European Union’s In Vitro Diagnostic Regulation (IVDR) is bringing together several changes to compliance requirements for laboratories. All laboratories with medical devices and lab-developed tests (LDTs) will need to comply with the general safety and performance requirements (GSPR) beginning May 26, 2022.

Twist Bioscience is committed to helping you navigate through the regulatory transition process to ensure compliance with IVDR.

Twist is partnering with platomics to help you understand your GSPR obligations.
Watch the webinar below to learn how Twist,
and our partner Platomics, can help you comply with the GSPR requirements

In-vitro Diagnostic Regulation is here.

Are you ready for IVDR?

Twist Bioscience is committed to helping you navigate through the regulatory transition process to ensure compliance with IVDR.

Need to get access to the GSPR checklist?

Want to learn more about how to meet your GSPR obligations?

Get In Touch With Us

Genes

Oligo Pools

NGS Target Enrichment Solutions

Variant Libraries

Antibody Discovery

In-vitro Diagnostic Regulation is here.

Are you ready for IVDR?

Twist Bioscience is committed to helping you navigate through the regulatory transition process to ensure compliance with IVDR.

Need to get access to the GSPR checklist?

Want to learn more about how to meet your GSPR obligations?

Get In Touch With Us