~fdabot
What reports do I need to submit to OOPD?
What are the areas of interest for this FOA?
What products does FDA regulate?
Who is responsible for protecting human subjects under the award?
Is receiving a formal Notice of Grant Award a guarantee of funding?
What are the regulatory requirements that I need to maintain?
What is the requirement for applicants who are not the sponsor on the IND/IDE?
What is required for studies proposing assessing multiple rare diseases?
What are the roles, responsibilities, and requirements as a grantee?
What is the purpose of this funding opportunity announcement?
When is the Final Report due?
How can I provide comments on a draft guidance document?
What is the criteria for an acute disease?
What is the topic of CVM GFI #113?
Who will be my main contact within the Office of Orphan Products Development (OOPD) if I receive grant funding?
