Scientific Validation
Scientific evaluation is a key component of any Biotech/Pharma investment, or licensing deal.
Smart Assays offers focused reproduction of major findings and proof of concept aimed at project validation.
Thus decreasing investors’ risks, in a time and cost efficient way.
Validation at Smart Assays
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Authentication and verification of biological results
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Reproduction of experiments
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Evaluation of drug candidates
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Examination of suggested development directions and targets
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When needed, further proof-of-concept experiment will be designed and performed
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Independent scientific assessment
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Comprehensive assessment of a technology’s potential, value and validity
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Industry work standards (internal QA)
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Design, create, document experiments
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Broad scientific support
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Working/Consultation with high level R&D experts
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Fully reproducible results
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Intellectual property obtained during due-diligence is client’s propriety
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FTE program for up to six months
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Tech transfer from academy
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Organization of materials by industry requirements
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Project feasibility
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Optimization and qualification of assays
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Full report and SOPs
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Tech transfer to client’s facility
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All work is performed according to key milestones and go/no-go stages
Advantages
Includes
Choosing to conduct your research with Smart Assays FTE program assures you:
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A PhD researcher
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100% committed to conducting your R&D
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Provided with constant scientific support and management
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Works within a state-of-the-art equipped laboratory in high level QA standards
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Full documentation for reproducibility
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At the end of the project, if so agreed, your FTE researcher can transfer to your facilities for implementation or for further work on the project
FTE - Your Scientist at Our Facilities
Scientific Validation
Validation Milestones
Month 1
Month 2-3
Month 4-5
Month 6
Literature review
Protocols writing and tech-transfer
Writing of scientific work plan
Feasibility
Optimization of protocols
Qualification
Depending on the project:
Full validation
Hits’ validation
Screening
Development of additional assays
SOPs and full report.
Start tech transfer to client’s facility