| Notice: 17565941 | |||
| Final Adopted Version in F.A.C. | |||
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| Department: | DEPARTMENT OF BUSINESS AND PROFESSIONAL REGULATION | ||
| Division: | Drugs, Devices and Cosmetics | ||
| Chapter: | Applications, Forms and Regulations | ||
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Overview |
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| RULE: |
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| RULE FILE DATE: | 5/20/2016 | ||
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| RULE EFFECTIVE DATE: | 6/9/2016 | ||
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| HISTORY NOTES: | Rulemaking Authority 499.012(3), 449.041(1)(a) FS. Law Implemented 499.01, 499.012, 499.0121, 499.015, 499.04, 499.041, 499.005(6), 499.0051(13), 499.051(1), 559.79 FS. History?New 6-9-16. | ||
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| OVERSIGHT COMMITTEE: | Joint Administrative Procedures Committee Florida Administrative Law Central Online Network (F.A.L.C.O.N.) |
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| RELATED COURT CASES: | Division of Administrative Hearings | ||
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| FEDERAL RULES
AND REGULATIONS: |
Electronic Code of Federal Regulations | ||
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| HOW TO LINK TO
THIS NOTICE: |
http://flrules.org/gateway/ruleno.asp?id=61N-2.014&Section=0 | ||
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| REFERENCE MATERIALS: |
Ref-06913 Application for Prescription Drug Manufacturer Permit |
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