Both the government agency and potential private sector partner identify mutual research interests and potential collaborative opportunities.

Preliminary discussions and meetings are held to align objectives, scope, and expectations.

The partners work together to draft a CRADA proposal, outlining the research aims, scope of work, resource commitments, intellectual property (IP) considerations, and timelines.

Key elements include project goals, roles and responsibilities, funding sources, and anticipated outcomes.

The budget should detail the contributions from both parties. This could include direct financial contributions, in-kind contributions (such as equipment, facilities, or personnel expertise), and any external funding sources.

Direct contributions involve actual funds provided by either party.

In-kind contributions refer to non-monetary resources provided, such as laboratory space, access to specialized equipment, or personnel time.

IRB: Responsible for reviewing and overseeing research involving human subjects to ensure ethical standards and compliance with regulatory requirements.

Its primary goal is to protect the rights, welfare, and privacy of human participants.

RDC: Provides oversight and strategic direction for the research and development activities within an organization, often within healthcare institutions like the VA.

Its goal is to ensure the alignment of research activities with organizational priorities and compliance with relevant regulations and standards.