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* 1. Contact Information

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* 2. How did you hear about BLOODPAC’s Generic Protocols for the Analytical Validation of Next-Generation Sequencing-Based ctDNA Assays?

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* 3. Have you used the protocols? If so, what sample types did you use for the analytical portion of your studies?

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* 4. Have you identified operational or technical challenges with using these protocols? If so, please explain as it relates to specific analytical studies or alteration types.

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* 5. Was there any guidance or method that you felt was missing from the protocols?

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* 6. What contrived sample models, if any,  did you use in conjunction with these protocols?

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* 7. How might these protocols help enable global clinical trials beyond the US?

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* 8. Please provide any comments, corrections, or edits to the protocols.

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