eloraRTGuidelines R4
eloraRTGuidelines R4
eloraRTGuidelines R4
Guidelines
Radiotherapy
Module
August 1, 2016
Contents
IMPORTANT UPDATES .................................................................................................................................................. 3
1 REGISTER INSTITUTE............................................................................................................................................. 4
7.1 REGULATORY PROCESSES FOR TELECOBALT AND GAMMA KNIFE INSTALLATION ................................................................... 17
7.2 REGULATORY PROCESSES FOR LINEAR ACCELERATOR INCLUDING TOMOTHERAPY AND CYBER KNIFE INSTALLATION..................... 18
7.3 REGULATORY PROCESSES FOR REMOTE AFTER LOADING BRACHYTHERAPY INSTALLATION (HDR/LDR/PDR/MDR) .................. 18
7.4 REGULATORY PROCESSES FOR MANUAL AFTER LOADING BRACHYTHERAPY INSTALLATION ..................................................... 19
7.5 REGULATORY PROCESSES FOR SIMULATOR AND CT SIMULATOR INSTALLATION ................................................................... 20
7.6 REGULATORY PROCESSES FOR KV IMAGING SYSTEM ....................................................................................................... 20
7.7 REGULATORY PROCESSES FOR IORT INSTALLATION........................................................................................................ 21
7.8 REGULATORY PROCESSES FOR CHECK SOURCE .............................................................................................................. 21
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10 SUBMISSION OF SAFETY STATUS REPORT............................................................................................................29
11.1 FOR LINEAR ACCELERATOR INCLUDING TOMOTHERAPY AND CYBER KNIFE ......................................................................... 33
11.2 FOR TELECOBALT AND GAMMA KNIFE ........................................................................................................................ 33
11.3 FOR REMOTE AFTER LOADING BRACHYTHERAPY (HDR/LDR/PDR/MDR) ....................................................................... 34
11.4 FOR SIMULATOR, CT SIMULATOR, KV IMAGING SYSTEM AND IORT SYSTEM ...................................................................... 34
11.5 FOR CHECK SOURCES/OPHTHALMIC APPLICATOR SOURCES ............................................................................................. 34
13 ANNEXURE C: FORMAT OF UNDERTAKING FOR RE-APPROVAL OF SITE AND LAYOUT PLAN ................................36
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eLORA Guidelines for Radiotherapy Module
eLORA module of Radiotherapy facilitate online submission of applications for regulatory consents
(layout approval/ authorization for procurement/Licence/Registration/RSO approval, etc.) for
Radiotherapy Facilities. All radiotherapy user Institutes are required to use eLORA system for obtaining
requisite regulatory clearance from AERB.
This document provides guidelines to use eLORA system for obtaining requisites regulatory consents
from AERB for Radiotherapy facility.
Important Note: Guidelines for common functionalities of eLORA system are available in Help menu
of eLORA. Users are also advised to refer these guidelines.
1 Register Institute
Visit home page of AERB website www.aerb.gov.in and click on the button eLORA. It will redirect you to
eLORA system.
Click on Register Institute (see above figure) link available on eLORA home page. This will open
application form for Institute Registration. Application form has three tabs.
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Important Note: Guidelines to fill application form for Institute Registration is available on eLORA
home page. It is advised to read the guidelines and keep soft copy of required attachments ready before
start filling of application form.
Fill the application form as per the guidelines. However, important points in each tab are mentioned
below:
Tab Institute Details:
Type of Institute: Select type of institute as either ‘Central Government’, ‘State Government’,
Private’ or ‘Joint Venture’.
In case the institute type is ‘Joint Venture’, Please upload dully filled scan copy of undertaking as given in
Annexure B: Format of undertaking for ‘Joint Venture’ institute, at the place given to upload ‘Other’
attachment in Tab: Attachments
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Type of Facility: In Type of Facility section, for the field Practice select Radiotherapy and for
the field Role of Institute select the role by clicking check box as shown in the below screen.
Multiple Check boxes can be chosen depending on the facilities proposed in your institution.
Important Note: Fields marked with * in the application form are mandatory. Application form will
not be submitted if any mandatory field left blank.
You will get acknowledgement message upon successful submission of application form. The copy of
submitted application (.pdf file) can be downloaded for which link will be provided (Please note, this link
will be active for a short period). You will also receive an acknowledgement mail with the copy of your
application form (.pdf file) in your email (email address as provided in the application form).
Application for Institute Registration will be scrutinized by AERB. After the approval of institute
registration by AERB, you will receive user ID and password in your registered email (email address of
Employer, as provided in the application form).
Existing Radiotherapy User Institutes should not apply for Institute Registration
Important Note: Existing user institutions which have obtained license for operation through hard
copy are preregistered by AERB and provided with user name and password. These institutions should
not apply for Institute Registration through eLORA. Any such existing institution which has not
received the user name and password may write to help email id [email protected]
Adding Other Roles (viz. Diagnostic Radiology, Nuclear Medicine, etc) in account
Important Note: In case you wish to add more practice/roles to your institution (such as adding
diagnostic radiology of nuclear medicine facilities in a registered radiotherapy institution) the same
can be done through the ‘Update Institution’ menu of eLORA.
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Important Note: Guidelines to fill application form for RP registration is available on e-LORA home
page. It is advised to read the guidelines and keep soft copy of required attachments ready before start
filling application form.
In case, your Institute has multiple profiles, system will ask you to select the Practice and Institute Role.
Please select Practice as “Radiotherapy” and Institute Role as “Radiation Facility”.
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4 Declaration of Instrument
Measuring (viz. Secondary Standard Dosimeter), Monitoring (Viz. Survey meter), QA and Safety Tools can
be declared one time in your eLORA account through Instrument Management menu. The status of
instruments (viz. proposed/available, update in calibration date, etc) can also be managed through this
menu.
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While adding instrument, it is important to mention availability of instrument i.e. either “Proposed” or
“Available”.
Detail of instrument required to be declared for each type of installation is given in Annexure A: List of
Requisite Instruments
Important Note: Regulatory clearances will not be issued till all requisite Measuring instruments,
Monitoring instruments, QA tools and Safety tools for particular type of facility are successfully
declared in eLORA.
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After clicking on “View Instrument” the following screen will appears. You can view details of all
instruments or update details of particular instrument or delete any particular Instrument from your
Institute account. Select the instrument and click on “View” as shown below.
After clicking on “view” the following screen will appear. Through this Employer of the Institute can
modify status of the instruments (viz. Functional status, Calibration date, Calibration valid till date,
Calibration energy and calibration lab detail). The selected equipment can also be deleted by clicking on
‘Delete’ button.
5 Declaration of Staff
Radiotherapy staff can be added in eLORA account through Menu: User Management Add Employee
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In drop down for Type of Employee, three options available as follows:
Radiation Worker (this is to add non-RP radiation workers viz. ward boy, nurse, etc working in
radiation area of radiotherapy department. PMS must be provided to such staff as detail of PMS
is mandatory for declaring Radiation Worker)
Non Radiation Worker (this is to add employee to be nominated as Licensee who is not a
radiation worker)
Radiation Professional (this is to add Radiation Professionals of Radiotherapy viz. Radiation
Oncologist, Medical Physicist, Radiotherapy Technologist and Radiotherapy Safety Professional)
While adding RP, system will ask RP registration ID and Date of birth of RP. (Obtain these details from
the Radiation Professional).
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In case RP is Employer of Institute, select ‘Yes’ for ‘Whether the person is also Employer of the
Institute?’
Provide Date of Joining (of service in your institute), PMS No. (i.e. complete TLD No.), Department
and Designation, Provide Email (O)
Browse and upload scan copy of joining /confirmation letter of employee and click on Submit
To upload “Attachment for uploading copy of Joining/Confirmation*”,you can attach a Scanned copy of
the Joining/confirmation letter of the added staff or a letter signed by the appropriate authority of the
facility mentioning the Name and Designation of all existing staff members working in the Radiotherapy
Department.
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populated automatically in the rest of the fields. Click on the button “Nominate”. The following screen will
appear:
Select the appropriate radiation facilities for which the candidate is to be nominated (as shown above).
After successful submission of form as per the standard procedure of eLORA (Please refer ‘General
Guidelines to use eLORA System’, available in eLORA Help menu), the form will be scrutinized by AERB.
After approval of the RSO Nomination, Employer and approved RSO will receive intimation email. A copy
of the approval letter will also be emailed to RSO’s email Id (O).
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On clicking on ‘renew’ button, the application form is generated which needs to be freezed and submitted
as per the standard procedure of eLORA i.e. Freeze Upload Signed PDF Submit. (Please refer ‘General
Guidelines to use eLORA System’, available in eLORA Help menu).
Click on ‘freeze’ button and submit the form as per standard procedure of eLORA (Please refer ‘General
Guidelines to use eLORA System’, available in eLORA Help menu).
In the “View employee list”, the status of RSO will be indicated as “No”.
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Relinquishing RSO from Institute
Important Note: In case the RSO is leaving the Institute, the employer has to “Undesignate” the
RSO first and then “Dissociate” him/her. A relinquishing letter for the RSO dissociation will be
available in RSO approval file and the status of the RSO file will be “close”.
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List of processes applicable to each type of installation is given below:
7.2 Regulatory processes for Linear Accelerator including Tomotherapy and Cyber Knife
installation
Steps Purpose Regulatory Form Name
First time Licence
Step 1. Obtaining site and layout approval Application for Site and Layout Approval
Step 2. Obtaining RSO approval Nominate RSO
Step 3. Obtaining procurement permission Application for Procurement (Equipment/Source)
of equipment
Step 4. Intimating receipt of equipment Equipment Receipt Intimation
Step 5. Obtaining commissioning approval Application for Commissioning
of equipment (i.e. prior permission
for switching ON beam)
Step 6. Submission of radiation survey Survey Report
levels measured around the
installation
Step 7. Obtaining licence for operation of Application for Licence
equipment
Renewal of Licence
Step 1. Renewal of existing Licence Renewal of Licence
Decommissioning
Step 1. Obtaining consent for Application for Decommissioning and Disposal
decommissioning
Step 2. Obtaining transport permission of Transport of Un-registered Source
Depleted Uranium (DU), if applicable
Step 3. Intimating disposal of Depleted Intimation of Export/Transport/Disposal
Uranium (DU), if applicable
Step 4. Intimating decommissioning of Intimation for Decommissioning
equipment
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Step 6. Obtaining authorization to supervise Source Supervision Authorization
source transfer operation
Step 7. Intimating receipt of radioactive Source Receipt Intimation
source
Step 8. For providing detail of source Source Transfer Report
transfer operation
Step 9. Obtaining commissioning approval Application for Commissioning
of equipment
Step 10. Submission of radiation survey Survey Report
levels measured around the
installation
Step 11. Obtaining licence for operation of Application for Licence
equipment
Renewal of Licence
Step 1. Renewal of existing Licence Renewal of Licence
Disposal of Disused Radioactive Source
Step 2. Obtaining transport permission of Transport of Registered Source
disused radioactive source
Step 3. Intimating disposal of radioactive Intimation of Export/Transport/Disposal
source
Re-procurement of Source
Step 1. Obtaining procurement permission Application for Procurement (Equipment/Source)
of radioactive source
Step 2. Intimating receipt of radioactive Source Receipt Intimation
source
Decommissioning and Disposal
Step 1. Obtaining consent for Application for Decommissioning and Disposal
decommissioning
Step 2. Obtaining transport permission of Transport of Registered Source
disused radioactive source
Step 3. Intimating disposal of radioactive Intimation of Export/Transport/Disposal
source
Step 4. Intimating decommissioning of Intimation for Decommissioning
equipment
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Step 1. Renewal of existing Licence Renewal of Licence
Re-procurement of Source
Step 1. Obtaining procurement permission Application for Procurement (Equipment/Source)
of radioactive source
Step 2. Intimating receipt of radioactive Source Receipt Intimation
source
Disposal
Step 1. Obtaining consent for disposal Application for Decommissioning and Disposal
Step 2. Obtaining transport permission of Transport of Registered Source
disused radioactive source
Step 3. Intimating disposal of radioactive Intimation of Export/Transport/Disposal
source
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Step 5. Obtaining licence for operation of Application for Licence
equipment
Renewal of Licence
Step 1. Renewal of existing Licence Renewal of Licence
Decommissioning
Step 1. Obtaining consent for Application for Decommissioning and Disposal
decommissioning
Step 2. Intimating decommissioning of Intimation for Decommissioning
equipment
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Step 3. Intimating disposal of radioactive Intimation of Export/Transport/Disposal
source
Important Note: Guidelines for preparation of Radiotherapy Site and Layout plan drawings available
in HELP menu of eLORA. Prepare the plan drawings in accordance with the guidelines.
Important Note: Accessories used in Linear Accelerator (viz. IMRT, VMAT, RapidArc, MLC, etc.) should
be selected in procurement for form equipment. In case of RapidArc or VMAT procurement, scan
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copy of separate request letter should be provided as an attachment while submitting
application form for procurement of medical accelerator.
Important Note: This form captures details of equipment received against procurement permission.
In this step user can selected the energies of equipment which has been received by them. For linear
accelerators, energies selected in this stage will be available for further regulatory processes like
commissioning, survey and license. Hence, submit this form after verification with the procurement
permission, to avoid any mismatch of details during later regulatory stages.
Important Note: This form captures details of radioactive source received against procurement
permission. In this step user can mention activity of radioactive source which has been received by
them. The data provided in this stage will be carry forwarded for further regulatory processes like
commissioning, survey, license, etc. Hence, submit this form after verification with the procurement
permission, to avoid any mismatch of details during later regulatory stages.
Important Note: In cases, Medical Physicist of the user institution never involved in source transfer
operation, the user institute can seek assistance of Medical Physicist (who has experience in source
transfer operation) from any other institute during source transfer operation. In such case, it is
mandatory to submit as an attachment, the letter of consent of the assisting Medical Physicist endorsed
by his/her employer.
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8.6 Source Transfer Report
This form is applicable for each source loading/unloading in Telecobalt and Gamma Knife equipment and
first time source loading in RAL Brachytherapy equipment. Submit this form to provide detail of source
transfer operation viz. date of source loading, detail of service engineer, detail of persons involved and
dose recorded in their pocket dosimeter. Follow below path to access this form:
Menu: Regulatory Form Radiotherapy Practice Source Transfer Report
Pre-requisite for source transfer report:
o Equipment Receipt Intimation
o Source Receipt Intimation
o Source Supervision Authorisation
Important Note
Only after obtaining Commissioning Approval from AERB, user shall energize the equipment to carry
out radiation survey.
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copy of Neutron Survey meter calibration certificate in Other Attachment section, in case of neutron
survey.
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Verify the detail of employees and instruments before submission of this form. In case, employee detail
and instrument detail is not up to date, update these details. Select ‘Equipment Type’ from drop down.
Logged-in user can see only those equipment/sources for which he/she is Licensee.
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Upload scan copy QA/QC report in option for “Upload the QA/QC report” and radiation survey data (in
Excel file) in option for “Upload the radiation survey report” respectively in Tab: “Attachment Details”.
B. Provide compliance status on Radiotherapy staff, PMS, measuring and monitoring tools and
security measures:
Submit the application form as per the standard procedure of eLORA i.e. Freeze Upload Signed PDF
Submit.
Important Note: In case of decommissioning of Telecobalt and Gamma Knife equipment, apply for
source supervision authorization after obtaining decommissioning approval from AERB.
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10.1 Update Operational Status of Sources and Equipment
Follow below path to access form to update operational status of each radioactive sources and
equipment:
Menu: Regulatory Form Common Forms Update Operational Status
Select ‘Radiation Generating Equipment’ for Linear Accelerator, Simulator, etc., ‘Equipment Housing
Source’ for Telecobalt, HDR, etc. and ‘Source’ for radioactive source. Then select ‘Identification No.’ from
the list of values. Serial No., Make and Model will be displayed automatically after selection of
‘Identification No’.
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The description to use for operational status is given below:
Operational Status Applicable to Description
Working Equipment and Radioactive Sources If equipment/radioactive source is
being used
Not Working Equipment If equipment is not working/not
being used
Disused Radioactive Sources If radioactive source is not being
used
Unused Radioactive Sources If radioactive source has never
been used
Temporarily Not in Use Equipment and Radioactive Sources If equipment/source is not being
used but intended to be used in
near future
Lost Equipment and Radioactive Sources If equipment/radioactive source is
lost
Sent for Repair Not applicable for Radiotherapy -
equipment
Follow the above procedure to update operational status of each radioactive source, equipment (i.e.
radiation generating equipment or equipment housing radioactive source(s)) one-by-one.
Select ‘Radiation Facility’ and click on ‘Radiotherapy-SSR-2015.xlsx’ to download the excel file.
Follow the below path to access form for Safety Status Report:
Menu: Regulatory Form Common Forms Safety Status Report
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The details of staff and measuring and monitoring instruments are displayed in first two tabs. Fill the
information as asked in tab: ‘Upload Safety Status Report’ and upload duly filled excel file in the upload
option for ‘Safety Status Report’.
Accept the undertaking by ticking on check box and press ‘Submit’ for submission of safety status report.
=O=O=O=O=O=
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11 Annexure A: List of Requisite Instruments
This gives list of measuring, monitoring, QA and safety tools required to be declared in Menu:
Instrument Management Add Instrument
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11.3 For Remote After Loading Brachytherapy (HDR/LDR/PDR/MDR)
List of Instruments Required to be declared in ‘Instrument Management’
Installation Type: Remote After Loading Brachytherapy
Type of Instrument Instrument Sub Type
Measuring Tools Large volume/well type ion chamber/Dose Calibrator
Thimble Chamber(as applicable)
Electrometer
Monitoring Tools Survey meter
Gamma zone monitor
QA Tools Thermometer
Barometer
Phantom for any specific QA(if applicable)
Safety Tools Emergency source storage
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12 Annexure B: Format of undertaking for ‘Joint Venture’ institute
Please submit undertaking in below format in Institute Registration application form if Institute to be
registered is ‘Joint Venture’ institute.
We, (names and addresses of beneficiaries), declare that we have made a joint venture to start
radiotherapy facility at (place address). (Elaborate on the proposed joint venture…..)
The land/premise, where the radiotherapy facility will be erected belongs to (name of
authorised person of land/premise (one of the beneficiaries)) and thereby, he/she will be the
employer and shall discharge the responsibilities of employer as per Atomic Energy (Radiation
Protection) Rules-2004. The employer will designate either himself/herself or nominate his/her own
employee as the licensee, who shall discharge the responsibility of licensee as per Atomic Energy
(Radiation Protection) Rules-2004.
Further, we undertake that in the event of any dispute, the equipment would be decommissioned
and the sources would be disposed off safely as per the procedures approved by the competent
authority.
Signature Signature
Name of Authorised Name of Authorised
person of land/premise: representative of other beneficiary:
Designation: Affiliation:
Name of the hospital:
Address: Address:
Date: Date:
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13 Annexure C: Format of undertaking for re-approval of site and layout plan
This undertaking is for layout plan(s) which was already approved through eLORA but needs re-
approval due to any of the reasons mentioned below in undertaking format. Since module for amendment
of layout plan is not yet developed in eLORA, therefore as an interim arrangement, institute needs to
furnish an undertaking in the below format while submitting application for re-approval through eLORA.
Format of undertaking to be submitted while applying for re-approval of layout plan after
submitting non-utilization of earlier approved plan
1. Details of earlier plan approval:
a) Case file No.:
b) Document No.:
c) Date of approval:
2. Re-approval is required due to following reasons:
a) In case of change in make and model:
Make and model as per earlier approval:______________________________________
Proposed make and model now:___________________________________
b) In case of change in the beam energy:
Beam energy(ies) as per earlier approval:_________________________________
Proposed beam energy(ies) now:______________________________________
c) Any other reason, kindly specify:________________________________
3. Due to above changes (tick wherever is applicable):
Name & signature of applicant: Name & signature of Head of the Institution:
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14 Annexure D: Undertaking to be submitted along with application for
commissioning
We hereby undertake that, we have compared the approved layout plan issued by AERB Vide
Application No.: ___________________document No.: ______________________dated___________________ with the
constructed Radiotherapy facility and found that all the walls, doors, partitions, nature of occupancy
all around the installation, construction materials and density etc. are same as approved by AERB.
We are fully aware that construction of bunker and/or modification in the approved layout plan
without prior approval of AERB is a violation of Atomic Energy (Radiation Protection) Rules, 2004 and
therefore, the license for operation issued by AERB liable to be revoked in case any deviation found in
future.
Name & signature of RSO Name & signature of Head of the Institution
==============================================================================
Undertaking from the Installation Engineer
Prior to installation of the radiotherapy equipment, I have verified that the design of the radiotherapy
facility and nature of occupancy all around the installation are in accordance with the above mentioned
layout plan approved by AERB.
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15 Annexure E: Frequently Asked Questions (FAQs)
Q. Our Institute is functioning under Central/State Government; whose detail should we furnish
for Employer?
Ans: Employer of an Institute is Head of Institute/Department who is responsible for execution of
duties of Employer as stipulated in Atomic Energy (Radiation Protection) Rules, 2004. Furnish detail
of your Head of Institute/ Department in Employer detail.
Q. Make and Model of equipment (e.g. Linear Accelerator, HDR, Telecobalt, CT Simulator, etc) is
being asked in site and layout application form but we have not decided make and model of
equipment so far for purchase, how to obtain layout approval?
Ans. You can apply for any similar equipment (for e.g. LA with same highest photon energy) so that
design requirement will not vary. At a later date, the site and layout approval can be regularised for
actual equipment you wish to purchase. Please see Re-approval of site and layout plan for more detail.
Q. Option of Linear Accelerator, Simulator, Manual After Loading Brachytherapy, etc (various
types of equipment/facilities) is not available in the drop down of 'Layout form submitted for'
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option in site and layout application form.
Ans: The options to select type of equipment in site and layout application form as well as application
forms related to various equipment types are visible based on your institute's profile (viz.
Radiotherapy) and role (viz. Linear Accelerator-Radiation Facility, etc). Please update your institute's
role to see various types equipment in drop down list and other application forms relevant to the role.
Use below path to update institute's role:
Menu: User Management --> Update institute details--> tab 'Institute detail', select additional
role by ticking check boxes and click on 'Update'
Q. My RSO application got rejected for incorrect entry of PMS/TLD no., how to correct PMS/TLD
no.?
Ans: Login through Employer's account, use following path Menu: 'User Management' -->
'Update/Dissociate Employee' --> Select Employee from 'Employee Details' --> click on 'Show
Details' --> Update your PMS No. --> click on 'Update'
(You can also update your Email address and Designation in the above Update Screen)
Q. I'm getting message 'Sorry, someone is already logged in this browser. Two person cannot
log in the same browser', what should I do?
Ans. This may happen when eLORA system is directly closed without logout. In such case, Please
restart your internet browser and access eLORA system.
Q. My RSO application got rejected for incorrect entry of PMS/TLD no., how to correct PMS/TLD
no.?
Ans: Login through Employer's account, use following path Menu: 'User Management' -->
'Update/Dissociate Employee' --> Select Employee from 'Employee Details' --> click on 'Show
Details' --> Update your PMS No. --> click on 'Update'
(You can also update your Email address and Designation in the above Update Screen)
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15.8 How to check status of application
Q. We have submitted application form through my eLORA account, I want to know its status?
Ans. The status of all application form can be seen through your account. After login, follow the Menu:
'My Applications'. You will see status in 'Application Status' for a given Application No.
Please note, only short informative messages are displayed in 'Inbox' (after login) about the
processing status of applications, use 'My Applications' to see the details of approval/rejection of
application.
For RENEWAL one must select “Renewal of Licence” and not “Application for Licence”
Q. I'm not able to see equipment/source in Licence renewal form?
Ans. Please check the name of Licensee of equipment/source in Menu (as shown below): My Institute
Details Tab 'Equipment' /Tab 'Radiation Sources'. Please login through the Licensee account of
respective equipment/source. Only current Licensee can submit application for renewal of
Licence.
Q. I'm not able to see Telegamma Therapy equipment or Remote After Loading Brachytherapy
(HDR/LDR/PDR/MDR) equipment in Licence renewal form?
Ans. At present, Telegamma Therapy equipment or Remote After Loading Brachytherapy
(HDR/LDR/PDR/MDR) equipment will not be available for renewal of Licence if no radioactive source
associated with the equipment having status “received”/”Licensed”. (Please check detail of associated
radioactive source in Menu: My Institute DetailsTab 'Radiation Sources’). In case the status of all the
radioactive sources associated with the equipment is “disposed”/“to be disposed”, the equipment will
not be available for renewal of Licence. However, application for renewal of licence can be submitted
after approval of Source Receipt Intimation of new source.
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Q. Licensee has forgotten eLORA account
‘Username’/’Password’, how to obtain it?
Ans. Use ‘Forgot Username’ or ‘Forgot Password’ option
available on eLORA home page as desired to obtain
Username or Password.
In case of any further difficulty, you can write to our help email address [email protected]
=O=O=O=O=O=
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