Investigational New Drug (IND) Submission checklist
If utilizing a drug that is currently subject to a manufacturer’s IND, or marketing application, refer to that IND or application or Drug Master File (if appropriate) to prevent duplicating information that are already available to FDA. Include a Letter of Authorization from the other sponsor permitting FDA to use their information for this IND. The Sponsor also must file a copy of the ... ................
................
To fulfill the demand for quickly locating and searching documents.
It is intelligent file search solution for home and business.
Related download
Related searches
- new home walk through checklist printable
- ind submission requirements fda
- ind submission checklist
- new drug for heart failure
- new drug for schizophrenia
- ind submission example
- fda new drug approval list
- fda new drug release
- fda ind submission process
- fda ind submission requirements
- fda ind submission timeline
- new build walk through checklist pdf