Fast, accurate and GxP compliant genome editing assessment
Brought to you by Data Curators BV
Brought to you by Data Curators BV
Use TIDE for quality assurance of gene-edited cell therapies and products, whether in research or in regulated environments.
TIDE was instrumental in getting Casgevy, the first CRISPR-based cell therapy, approved by the FDA.
Audits
Citations
Weekly users
Intended for non-commercial research
Target users: Academic scientists
Interface: GUI
Batch support: Up to 20 samples
Supported CRISPR enzymes: Cas9
Supported editing: HDR editing, NHEJ editing
Delivery method: SaaS
Designed for regulated research, clinical trials, and manufacturing processes, TIDE GxP encompasses the GLP, GCP, and GMP variants, tailored to meet specific compliance needs.
GLP: Non-clinical laboratory studies
GCP: Clinical trial management
GMP: Manufacturing process management
GLP: Scientists, lab managers, QA teams
GCP: Clinical trial managers, CROs, QA teams
GMP: Manufacturing managers, QC/QA teams
Graphical User Interface (GUI) and Command Line Interface (CLI) across all GxP versions
Unlimited across all versions
Cas9, Cas12
HDR editing, NHEJ editing
GLP: OECD GLP, FDA 21 CFR part 58
GCP: ICH GCP, FDA 21 CFR parts 50/312
GMP: FDA 21 CFR parts 210/211, EU GMP
Ensures accuracy, traceability of study, trial, and manufacturing data
Validation packs and patient safety mechanisms
On-premises or Private validated SaaS
Escrow service for all versions
Intended for commercial research
Target users: Scientists
Interface: GUI, CLI
Batch support: Unlimited
Supported CRISPR enzymes: Cas9, Cas12
Supported editing: HDR editing, NHEJ editing
Delivery method: On-premises or Private SaaS
We’re here to help you streamline your gene therapy development and achieve regulatory success. Whether you have questions or need guidance, our team is ready to support you every step of the way.
Reach out today and discover how TIDE GxP can empower your work!