Information Technology Dashboard - IT Department Performance Metrics

V

Valli

Involved In Discussions
#1
#1
Dear All,

Can someone suggest the IT Dash board or to measure department performance parameters.

Regards,
Valli
 
Standard Work Instruction Software by Dozuki
Elsmar Forum Sponsor
Jen Kirley

Jen Kirley

Quality and Auditing Expert
Staff member
Admin
#2
#2
Good day, I have questions please:

Is your IT Department managing the network?

If so, are the activities local or done on behalf of additional sites as a corporate function?

Do you have a help desk?
 
V

Valli

Involved In Discussions
#3
#3
Jen Kirley said:
Good day, I have questions please:

Is your IT Department managing the network?

If so, are the activities local or done on behalf of additional sites as a corporate function?

Do you have a help desk?
Click to expand...
Good day, I have questions please:

Is your IT Department managing the network?
Yes

If so, are the activities local or done on behalf of additional sites as a corporate function?
locally
Do you have a help desk?
yes
 
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
F Information Technology in IATF 16949 audit scope IATF 16949 - Automotive Quality Systems Standard 12
E ISO 9001:2015 for Information Technology Department Human Factors and Ergonomics in Engineering 2
P Seeking Information on ISO 15504 - Information Technology Process Assessment Other ISO and International Standards and European Regulations 3
Richard Regalado ISO/IEC 27000:2014 - Information technology - Overview and vocabulary (FREE download) IEC 27001 - Information Security Management Systems (ISMS) 4
S Information Technology Department (IT) Checklist for ISO 9001:2008 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
B ITIL (Information Technology Infrastructure Library) Foundation Certificate Career and Occupation Discussions 1
A Information Technology Process Mapping per ISO 13485 - example wanted Process Maps, Process Mapping and Turtle Diagrams 1
S External Documents in the I.T. (Information Technology) Field ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
A Non Conforming Product in an IT (Information Technology) Company ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
Q What ISO 9001:2008 procedures apply for IT (Information Technology)? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 21
A ISO 20001 (ITIL) Information Technology Infrastructure Library IT (Information Technology) Service Management 2
L Auditing Information Technology (IT) in the ISO 9001 workplace Internal Auditing 15
M Information Technology Record Retention time best practices Quality Management System (QMS) Manuals 2
D Internal Audit of Information Technology Internal Auditing 8
D Information Technology Process Audit - Suggestions for Auditing IT IATF 16949 - Automotive Quality Systems Standard 12
C Understanding Concepts of Information Technology & Infrastructure Library (ITIL) Misc. Quality Assurance and Business Systems Related Topics 1
netwizard Looking for an ISO 9001:2000 Internal Audit Checklist - UOP (Information Technology) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
A QMS For IT (information Technology) Sector ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
R Risk assessment on IT containers and the information they contain IEC 27001 - Information Security Management Systems (ISMS) 4
O EN 301 489-1 and EN 301 489-17 - Where do we get the information of the Published versions? CE Marking (Conformité Européene) / CB Scheme 1
K Article 18: Implant Card and information to be communicated. EU Medical Device Regulations 5
K EU MDR Annex 1 Chapter III: Information in the Instructions for Use-23.4 (e) the performance characteristics of the device; EU Medical Device Regulations 1
A GMDN Registration Basic preliminary Information EU Medical Device Regulations 0
J Controlled information versus defined documents / records ISO 13485:2016 - Medical Device Quality Management Systems 3
A Medical device Reporting : Good Faith Effort for Additional information Other US Medical Device Regulations 2
P Cenelec updated standard information CE Marking (Conformité Européene) / CB Scheme 1
Richard Regalado Automotive News TISAX - VDA ISA (information security assessment) VDA Standards - Germany's Automotive Standards 5
JoCam False information provided for Medical Device Registration - What are the implications? Other Medical Device Related Standards 3
adir88 Information of safety can reduce risk now? ISO 14971 - Medical Device Risk Management 12
Richard Regalado What could go wrong with information: Ransomware statistics and facts (2018 to present) IEC 27001 - Information Security Management Systems (ISMS) 0
Q LOT or Serial Number Symbol not used when the information is contained in the UDI? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
A Information about Medical Device Test Laboratories Other Medical Device and Orthopedic Related Topics 4
C Missing routers/documented information Nonconformance and Corrective Action 5
MrTetris Unacceptable risk and information for safety ISO 14971 - Medical Device Risk Management 16
M Is Harmonised EN 1041 (Information Supplied By Manufacturer) Worth Looking At? EU Medical Device Regulations 7
P Predicate Device Information for 510(k) Submission Medical Device and FDA Regulations and Standards News 4
V IS/ISO/IEC 17025:2017 Clause 7, sub clause 7.11 Control of data and information management ISO 17025 related Discussions 1
A Medical Device Contract Manufacturing Requirements and Information - Help wanted ISO 13485:2016 - Medical Device Quality Management Systems 5
H Analog Pressure Gauge with no EN837 accuracy class information General Measurement Device and Calibration Topics 5
M Informational EU – MDCG 2019-12 Designating authority’s final assessment form: Key Information Medical Device and FDA Regulations and Standards News 0
G What information to put on measurement Dimensional Results APQP and PPAP 7
L MDR - Information in the instructions for use - clausole 23.4.(z) EU Medical Device Regulations 2
K AS9100D Clause 7.5.2.a) - What is considered to be "documented information"? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
A Information on good laboratory practices (GLP) for the non-medical or food industry wanted Manufacturing and Related Processes 1
I What kind of information needs to be in a calibration record? General Measurement Device and Calibration Topics 25
M Informational TGA – Medical device patient information leaflets and implant cards Medical Device and FDA Regulations and Standards News 0
Q AS9120 7.5.3.2 Control of Documented Information - Audit Nonconformance AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 20
G Posting Measuring Equipment Accuracy for User Information General Measurement Device and Calibration Topics 4
J EC REP information and CE Mark - Component of a system that is not a medical device EU Medical Device Regulations 2
M Informational EU – Medical devices: Implementation of Regulation (EU) 2017/745 on medical devices (MDR) – Information from the Irish and German delegations Medical Device and FDA Regulations and Standards News 0

Similar threads

Top Bottom