New GLP AAV-ITR Sequencing for FDA Submissions
GENEWIZ’s proprietary AAV-ITR Sanger sequencing is now available as a GLP-compliant (21 CFR part 58) workflow to support FDA IND, NDA, and BLA submissions. Our unique protocol sequences through difficult inverted terminal repeat (ITR) regions of adeno-associated virus (AAV), prevents abrupt reduction in the sequencing signal at the start of the ITR hairpin, and reads through the full length of the ITR region. Check out our tech note for more information on our proprietary AAV-ITR Sanger sequencing protocol.
Increased read lengths and improved data quality allow for early detection of point mutations
Proprietary GLP-level AAV-ITR method provides greater ITR sequencing coverage compared to standard protocols
Dedicated Study Director for proactive, transparent communication throughout your entire project
Final report includes a description of methods, list of SOPs, raw data, detailed analysis, signed GLP compliance statement, and QA inspections
Complete solutions pipeline from nucleic acid extraction to data analysis
Assay development expertise excelling in assay optimization and handling difficult templates
Industry-leading turnaround with options for expedited assay development and sequencing
State-of-the-art GLP laboratory with Quality Assurance Unit oversight ensures your project will meet FDA guidelines
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