Fla. Admin. Code Ann. R. 64E-5.626 - Use of Radiopharmaceuticals for Uptake, Dilution, or Excretion Studies
A licensee is allowed to use any unsealed radioactive material in a radiopharmaceutical for a diagnostic use involving measurements of uptake, dilution, or excretion for medical use under the following conditions:
(1) When a written
directive is not required by subsection
64E-5.607(3),
F.A.C., the licensee must satisfy the following:
(a) Radioactive material is obtained from a
manufacturer or pharmacy licensed as specified in subsection
64E-5.210(10),
F.A.C., or in equivalent NRC or agreement state regulations, or
(b) Radioactive material is obtained from and
prepared by a NRC or agreement state licensee for use in research in accordance
with a Radioactive Drug Research Committee-approved protocol, or a Notice of
Claimed Investigational Exemption for a New Drug (IND) protocol accepted by
U.S. Food and Drug Administration (FDA), or
(c) Radioactive material is prepared by the
licensee for use in research in accordance with a Radioactive Drug Research
Committee-approved application, or an IND protocol accepted by FDA,
or
(d) Radioactive material is
prepared by:
1. An authorized nuclear
pharmacist,
2. Except for sodium
iodide I-131 in quantities greater than 30 microcuries (1.11 MBq), a physician
who is an authorized user and meets the training requirements specified in Rule
64E-5.650 or
64E-5.660, and sub-subparagraph
64E-5.650(3)(a)
2.g., F.A.C., or
3. An individual
under the supervision of a physician who is an authorized user under
subparagraph 64E-5.626(1)(d)
2., F.A.C., and as specified in paragraphs
64E-5.601(3)(a) and
(b),
64E-5.607(3)(e),
or subsection 64E-5.608(1),
F.A.C., or
(2) When a written
directive is required by subsection
64E-5.607(3),
F.A.C., the licensee must satisfy the following:
(a) Radioactive material is obtained from a
manufacturer or pharmacy licensed as specified in subsection
64E-5.210(10),
F.A.C., or in equivalent NRC or agreement state regulations, or
(b) Radioactive material is obtained from and
prepared by an NRC or agreement state licensee for use in research in
accordance with a Radioactive Drug Research Committee-approved protocol or an
IND protocol accepted by FDA, or
(c) Radioactive material is prepared by the
licensee for use in research in accordance with a Radioactive Drug Research
Committee-approved application, or an IND protocol accepted by FDA,
or
(d) Radioactive material is
prepared by:
1. An authorized nuclear
pharmacist,
2. A physician who is
an authorized user and meets the training requirements specified in Rule
64E-5.650 or
64E-5.660, F.A.C., or
3. An individual under the supervision of a
physician who is an authorized user under subparagraph
64E-5.626(1)(d)
2., F.A.C., and as specified in paragraphs
64E-5.601(3)(a) and
(b),
64E-5.607(3)(e)
or subsection 64E-5.608(1),
F.A.C.
Notes
Rulemaking Authority 404.051, 404.061, 404.071, 404.081, 404.141 FS. Law Implemented 404.022, 404.051(1), (4), (5), (6), (8), (9), (10), (11), 404.061(2), (3), 404.071(1), 404.081, 404.141 FS.
New 8-25-91, Formerly 10D-91.733, Amended 8-6-01, 2-11-10, 12-26-13.
State regulations are updated quarterly; we currently have two versions available. Below is a comparison between our most recent version and the prior quarterly release. More comparison features will be added as we have more versions to compare.
A licensee is allowed to use any unsealed radioactive material in a radiopharmaceutical for a diagnostic use involving measurements of uptake, dilution, or excretion for medical use under the following conditions:
(1) When a written directive is not required by subsection 64E-5.607(3), F.A.C., the licensee must satisfy the following:
(a) Radioactive material is obtained from a manufacturer or pharmacy licensed as specified in subsection 64E-5.210(10), F.A.C., or in equivalent NRC or agreement state regulations, or
(b) Radioactive material is obtained from and prepared by a NRC or agreement state licensee for use in research in accordance with a Radioactive Drug Research Committee-approved protocol, or a Notice of Claimed Investigational Exemption for a New Drug (IND) protocol accepted by U.S. Food and Drug Administration (FDA), or
(c) Radioactive material is prepared by the licensee for use in research in accordance with a Radioactive Drug Research Committee-approved application, or an IND protocol accepted by FDA, or
(d) Radioactive material is prepared by:
1. An authorized nuclear pharmacist,
2. Except for sodium iodide I-131 in quantities greater than 30 microcuries (1.11 MBq), a physician who is an authorized user and meets the training requirements specified in Rule 64E-5.650 or 64E-5.660, and sub-subparagraph 64E-5.650(3)(a) 2.g., F.A.C., or
3. An individual under the supervision of a physician who is an authorized user under subparagraph 64E-5.626(1)(d) 2., F.A.C., and as specified in paragraphs 64E-5.601(3)(a) and (b), 64E-5.607(3)(e), or subsection 64E-5.608(1), F.A.C., or
(2) When a written directive is required by subsection 64E-5.607(3), F.A.C., the licensee must satisfy the following:
(a) Radioactive material is obtained from a manufacturer or pharmacy licensed as specified in subsection 64E-5.210(10), F.A.C., or in equivalent NRC or agreement state regulations, or
(b) Radioactive material is obtained from and prepared by an NRC or agreement state licensee for use in research in accordance with a Radioactive Drug Research Committee-approved protocol or an IND protocol accepted by FDA, or
(c) Radioactive material is prepared by the licensee for use in research in accordance with a Radioactive Drug Research Committee-approved application, or an IND protocol accepted by FDA, or
(d) Radioactive material is prepared by:
1. An authorized nuclear pharmacist,
2. A physician who is an authorized user and meets the training requirements specified in Rule 64E-5.650 or 64E-5.660, F.A.C., or
3. An individual under the supervision of a physician who is an authorized user under subparagraph 64E-5.626(1)(d) 2., F.A.C., and as specified in paragraphs 64E-5.601(3)(a) and (b), 64E-5.607(3)(e) or subsection 64E-5.608(1), F.A.C.
Notes
Rulemaking Authority 404.051, 404.061, 404.071, 404.081, 404.141 FS. Law Implemented 404.022, 404.051(1), (4), (5), (6), (8), (9), (10), (11), 404.061(2), (3), 404.071(1), 404.081, 404.141 FS.
New 8-25-91, Formerly 10D-91.733, Amended 8-6-01, 2-11-10, 12-26-13.