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EDITED - Radiation Protection Manual Template
EDITED - Radiation Protection Manual Template
*Facilit FACILITY*
y *Address*
Logo* *Contact Information*
NOTE: You may use your own formatting but please ensure that the
contents seen in this template are reflected on the radiation
protection manual you will be submitting.
RADIATION
PROTECTION
MANUAL
DEPARTMENT OF RADIOLOGY
Table of Contents
Prepared by : Signature
*Name*
*Position*
Reviewed by : Signature
*Name*
*Position*
Approved by : Signature
*Name*
*Position*
A. Controlled Area
Describe/define a controlled area in terms of radiation protection inside the
facility. After defining, list/enumerate the controlled areas.
B. Supervised Area
Title Radiation Protection Manual Date Prepared *27 September
2022*
Document No. *Please provide* Date Reviewed *28 September
2022*
Revision No. *Please provide* Date Approved *29 September
2022*
Page 5 of 19 Date Effective *30 September
2022*
*NAME OF YOUR
*Facilit FACILITY*
y *Address*
Logo* *Contact Information*
A. Radiation Workers
The worker is entitled for dose monitoring. It is the nature of his/her job to
manage and control x – ray radiation. Hence, dose monitoring is required and
the dose monitoring mechanism shall be a/an *x* (choose whether x is Optically
Stimulated Luminescence or Thermoluminescent Dosimeter) badge. One badge
shall be named and designated for each worker. Workers are, but shall not be
limited to, radiologic/x – ray technologist/s and radiologist/s.
D. Pediatric Patients
(If "no" for dose monitoring) Pediatric patients are not entitled for dose
monitoring. There are no dose limits for patients since exposures are necessary
and justified to diagnose medical conditions. The benefit of exposure outweighs
the negative effects of exposure. Hence, dose monitoring is optional for
pediatric patients.
A. Pregnant Patient
(If allowed, remove if not allowed) The facility permits the x – ray examination
of pregnant patient as long as the following conditions are met:
o Condition 1
o Condition 2
o Condition 3
o Condition 4
o Condition 5
o (Include additional/relevant conditions if necessary)
OR
(If not allowed, remove if allowed) The facility does not permit the x – ray
examination of pregnant patients.
B. Pregnant Worker
(If allowed, remove if not allowed) The facility permits a pregnant worker to
operate or control/be near an x – ray equipment as long as the following
conditions are met:
o Condition 1
o Condition 2
o Condition 3
o Condition 4
o Condition 5
o (Include additional conditions if necessary)
OR
(If not allowed, remove allowed) The facility does not permit a pregnant worker
to operate or control/be near an x – ray equipment. The facility shall relieve the
pregnant worker from the operation of x – ray room and shall transfer her to areas
with low/no risk of exposure to x – ray radiation.
3.5.1.8 Procedure 8
3.5.1.9 Procedure 9
3.5.1.10 Procedure 10
3.5.1.11 (Include more additional procedures)
3.5.2 Pregnant Radiation Worker (if facility allows x – ray equipment operation by
pregnant worker; otherwise, remove)
3.5.2.1 Procedure 1
3.5.2.2 Procedure 2
3.5.2.3 Procedure 3
3.5.2.4 Procedure 4
3.5.2.5 Procedure 5
3.5.2.6 Procedure 6
3.5.2.7 Procedure 7
3.5.2.8 Procedure 8
3.5.2.9 Procedure 9
3.5.2.10 Procedure 10
3.5.2.11 (Include more additional procedures)
3.5.4 Pregnant Patient (if facility allows x – ray examination of pregnant patient;
otherwise, remove)
3.5.4.1 Procedure 1
3.5.4.2 Procedure 2
3.5.4.3 Procedure 3
3.5.4.4 Procedure 4
3.5.4.5 Procedure 5
3.5.4.6 Procedure 6
3.5.4.7 Procedure 7
3.5.4.8 Procedure 8
3.5.4.9 Procedure 9
3.5.4.10 Procedure 10
3.5.4.11 (Include more additional procedures)
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Title Radiation Protection Manual Date Prepared *27 September
2022*
Document No. *Please provide* Date Reviewed *28 September
2022*
Revision No. *Please provide* Date Approved *29 September
2022*
Page 14 of 19 Date Effective *30 September
2022*
*NAME OF YOUR
*Facilit FACILITY*
y *Address*
Logo* *Contact Information*
7 ? ? ?
A. The designated radiation protection officer shall report the incident report of
overdosing of either patient or worker to the regulators of man – made radiation,
the Center for Device Regulation, Radiation Health, and Research of the Food and
Drug Administration.
a. Date of report
b. Name of facility
c. Name of individual exposed
d. Age
e. Sex
f. Type of exposed individual (patient, worker, or public)
g. Date of over – exposure incidence
h. Dose obtained (if worker which is based on OSL/TLD report by service
provider)
i. Clinical manifestation
j. Statement of the scenario of over – exposure
k. Immediate action plans undertaken by facility
l. Corrective/preventive actions undertaken by facility
m. Supports/risk communication plans undertaken by facility to the exposed
individual
n. Name and signature of the radiation protection officer who made the report
o. Name and signature of the legal person who acknowledged/noted the report
4.0 References
o Food and Drug Administration Circular No. 2020 – 035 Annex D
Page 2
o Reference No. 2
o Reference No. 3
o Reference No. 4
o Reference No. 5
o Reference No. 6
o Reference No. 7
o Reference No. 8
o Reference No. 9
o Reference No. 10
o (Include more additional references)
10