61N-2.011. Application for Nonresident Prescription Drug Manufacturer Permit

A nonresident prescription drug manufacturer permit is required for any person, located outside of Florida, that is a manufacturer of a prescription drug and that engages in the distribution of such prescription drug into Florida. A person engaging in activity for which a nonresident prescription drug manufacturer permit is required, must file an application on form number DBPR-DDC-202, Application for Permit as a Nonresident Prescription Drug Manufacturer, effective February 2017, adopted and incorporated herein by reference and comply with all the requirements for permitting in Chapter 499, F.S., and Rule Title 61N, F.A.C. This form is available upon request from the Division of Drugs, Devices and Cosmetics at 2601 Blair Stone Road, Tallahassee, Florida 32399-1047, [phone], or at http://www.flrules.org/Gateway/reference.asp?No=Ref-08056.

Rulemaking Authority 499.01, 499.012, 499.0121, 499.04, 499.041, 499.05 FS. Law Implemented 499.01, 499.012, 499.0121, 499.015, 499.04, 499.041, 499.05, 559.79 FS. History‒New 5-11-17.