Generate a Statement of Work detailing phased laboratory protocols and intellectual-property handling for a multi-institutional CRISPR gene-editing research project that spans oncology and infectious-disease applications

Generate generate a statement of work detailing phased laboratory protocols and intellectual-property handling for a multi-institutional crispr gene-editing research project that spans oncology and infectious-disease applications for Scientific Research and Development Services industry

Scientific Research and Development Services

Agent Configuration

Login required: You need to sign in to execute this agent.

Click to upload or drag and drop

Allowed: PDF, DOCX, TXT, XLSX

Max size: 50MB

Upload existing research protocols, prior SOWs, or collaborative research agreements that will inform the new Statement of Work
Select the primary disease applications for CRISPR gene-editing research
List all participating institutions, their roles (academic, commercial, clinical), and key contact personnel
Select the primary FDA regulatory classification for the proposed CRISPR applications
Define intellectual property ownership and licensing structure for generated IP
Specify research phases, duration estimates, and clear deliverable milestones for each institution
Select applicable quality management systems and regulatory standards
Specify materials requiring MTAs: cell lines, animal models, vectors, reagents, and associated biosafety levels
Define publication rights and data sharing timeline with embargo periods
Detail budget distribution across institutions, including indirect costs, equipment purchases, and personnel allocations
Select the comprehensive risk assessment framework for biological, technical, and regulatory risks
Include any additional requirements: international shipping (ITAR/EAR), participant compensation, special containment needs, or cross-institutional training programs