Application for Nonresident Prescription Drug Manufacturer Permit

 

DEPARTMENT OF BUSINESS AND PROFESSIONAL REGULATION

Drugs, Devices and Cosmetics

RULE NO.:RULE TITLE:

61N-2.011Application for Nonresident Prescription Drug Manufacturer Permit

NOTICE OF CHANGE

Notice is hereby given that the following changes have been made to the proposed rule in accordance with subparagraph 120.54(3)(d)1., F.S., published in Vol. 43 No. 22, February 2, 2017 issue of the Florida Administrative Register. The changes are in response to written comments submitted by the staff of the Joint Administrative Procedures Committee. The changes are as follows:

 

Section VI, Page 8, Numbers 2 and 3:

The Department will revise the Application for Nonresident Prescription Drug Manufacturer Permit, Form number DBPR-DDC 202 to conform to the statutory language in Chapter 499.01(2)(c). By changing the word “state” to “jurisdiction”

 

THE PERSON TO BE CONTACTED REGARDING THIS CHANGE IS: Dinah Greene, Operations Review Specialist, Division of Drugs, Devices and Cosmetics, Department of Business and Professional Regulation, 2601 Blair Stone Road, Tallahassee, Florida 32399-1047; [phone]; [e-mail].