Form DBPR-DDC-202 Application for Permit as a Nonresident Prescription Drug Manufacturer - Florida

What Is Form DBPR-DDC-202?

This is a legal form that was released by the Florida Department of Business & Professional Regulation - a government authority operating within Florida. As of today, no separate filing guidelines for the form are provided by the issuing department.

FAQ

Q: What is DBPR-DDC-202?
A: DBPR-DDC-202 is the application form for a permit as a nonresident prescription drug manufacturer in Florida.

Q: Who can use this form?
A: This form is for nonresident prescription drug manufacturers who want to obtain a permit in Florida.

Q: What is the purpose of this permit?
A: The permit allows nonresident prescription drug manufacturers to distribute their products in Florida.

Q: Are there any fees associated with this application?
A: Yes, there is an application fee which must be submitted along with the completed form.

Q: Is there a deadline for submitting this application?
A: There is no specific deadline for submitting the application, but it is recommended to submit it well in advance to allow for processing time.

Q: How long does it take to process this application?
A: The processing time for this application can vary, but it usually takes several weeks.

Q: What documents are required to accompany this application?
A: The application must be accompanied by several documents, including a copy of the manufacturer's federal registration, a current Good Manufacturing Practices (cGMP) certificate, and a Surety Bond or Irrevocable Letter of Credit.

Q: Who should I contact for more information about this application?
A: For more information about the DBPR-DDC-202 application, you can contact the Florida Department of Business and Professional Regulation (DBPR).