VARIAN

medical systems

RapidArc
QA Test Procedures
Calculation Spreadsheet

P1012382-001-A FEBRUARY 2015

 A B C D E F G H I

1
Image Analysis using 10 cm x 0.5 cm ROI
2

3 Dose Rate - Gantry Speed Test

4
Band number - 6 cm -4 cm -2 cm 0 cm 2 cm 4 cm 6 cm Threshold

5
RDR-GS
6
ROpen
7
Rcorr #DIV/0! #DIV/0! #DIV/0! #DIV/0! #DIV/0! #DIV/0! #DIV/0!
8
Diff(x) #DIV/0! #DIV/0! #DIV/0! #DIV/0! #DIV/0! #DIV/0! #DIV/0! < ±3%

10
Average of absolute deviations (DiffAbs) #DIV/0! <1.5%

P1012382-001-A RapidArc QA Test Procedures Calculation Spreadsheet

Image Analysis using 10 cm x 0.5 cm ROI

Leaf Speed Test

Band number -4.5 cm -1.5 cm 1.5 cm 4.5 cm Threshold

RLS
ROpen
Rcorr #DIV/0! #DIV/0! #DIV/0! #DIV/0!

Diff(x) #DIV/0! #DIV/0! #DIV/0! #DIV/0! < ±3%

Average of absolute deviations (DiffAbs) #DIV/0! <1.5%

P1012382-001-A RapidArc QA Test Procedures Calculation Spreadsheet

Document ID P1012382, Revision 001-A

Document Title RapidArc QA Test Procedures Calculation Spreadsheet

Abstract This spreadsheet provides information for RapidArc QA tests. This document is the English-language original.

Manufacturers
Varian Medical Systems, Inc.
3100 Hansen Way
Palo Alto, CA 94304-1038
USA

Varian Medical Systems UK Ltd.

Oncology HouseGatwick Road, Crawley
European Authorized
West Sussex RH10 9RG
Representative
United Kingdom

Notice Information in this release note is subject to change without notice and does not represent a commitment on the
part of Varian. Varian is not liable for errors contained in this release note or for incidental or consequential
damages in connection with furnishing or use of this material.

This document contains proprietary information protected by copyright. No part of this document may be
reproduced, translated, or transmitted without the express written permission of Varian Medical Systems, Inc.

FDA 21 CFR 820 Quality System Varian Medical Systems, Oncology Systems products are designed and manufactured in accordance with the
Regulation requirements specified within this federal regulation.
(cGMPs)

ISO 13485 Varian Medical Systems, Oncology Systems products are designed and manufactured in accordance with the
requirements specified within the ISO 13485 quality standard.

CE Varian Medical Systems, Oncology Systems products meet the requirements of Council Directive MDD
93/42/EEC.

EU REACH SVHC Disclosure The link to the current EU REACH SVHC disclosure statement is:

http://www.varian.com/us/corporate/legal/reach.html
HIPAA Varian’s products and services are specifically designed to include features that help our customers comply with
the Health Insurance Portability and Accountability Act of 1996 (HIPAA). The software application uses a secure
login process, requiring a user name and password that supports role-based access. Users are assigned to
groups, each with certain access rights, which may include the ability to edit and add data or may limit access to
data. When a user adds or modifies data within the database, a record is made that includes which data were
changed, the user ID, and the date and time the changes were made. This establishes an audit trail that can be
examined by authorized system administrators.

WHO ICD-O codes and terms used by permission of WHO, from:

n International Classification of Diseases and for Oncology (ICD-O), 3rd edition, Geneva, World Health
Organization, 2000.

ICD-10 codes and terms used by permission of WHO, from:

n International Statistical Classification of Diseases and Related Health Problems, Tenth Revision (ICD-10).
Vols 1–3, Geneva, World Health Organization, 1992.

CAUTION US Federal law restricts this device to sale by or on the order of a physician.

Trademarks RapidArc is a registered trademark of Varian Medical Systems, Inc. All other trademarks or registered
trademarks are the property of their respective owners.

Copyright © 2015 Varian Medical Systems, Inc.

Arc QA tests. This document is the English-language original.

ge without notice and does not represent a commitment on the

ined in this release note or for incidental or consequential
his material.

rotected by copyright. No part of this document may be

express written permission of Varian Medical Systems, Inc.

ducts are designed and manufactured in accordance with the

on.

ducts are designed and manufactured in accordance with the

ity standard.

ducts meet the requirements of Council Directive MDD

ure statement is:

al/reach.html
esigned to include features that help our customers comply with
y Act of 1996 (HIPAA). The software application uses a secure
rd that supports role-based access. Users are assigned to
ay include the ability to edit and add data or may limit access to
he database, a record is made that includes which data were
changes were made. This establishes an audit trail that can be

HO, from:
for Oncology (ICD-O), 3rd edition, Geneva, World Health

WHO, from:
eases and Related Health Problems, Tenth Revision (ICD-10).
992.

or on the order of a physician.

dical Systems, Inc. All other trademarks or registered

wners.