ISAGO - IATA Safety Audit for Ground Operations

J

joshua_sx1

#1
:bigwave: Hello guys & gals… I'm now involved with the development of ISAGO (IATA Safety Audit for Ground Operations) to our operations…

Any inputs from “experts” and “becoming an expert” would be highly appreciated. :cool:

My first inquiry is the ISAGO Standard Manual which composed of 10 Sections as follows:

Section 1: Organization & Management System (OMS)
Section 2: Station Management (STM)
Section 3: Load Control (LOD)
Section 4: Passenger Handling (PAX)
Section 5: Baggage Handling (BAG)
Section 6: Aircraft Handling & Loading (HDL)
Section 7: Aircraft Ground Movement (AGM)
Section 8: Cargo Handling (CGM)
Section 9: Aircraft Fueling (FUL)
Section 19: Aircraft De/Anti-Icing (DEI)

I’m wondering if someone could share a sample format of the first two sections…

Thanks for any inputs… :agree1:
 
Elsmar Forum Sponsor

Randy

Super Moderator
#2
You might be able to get some free stuff if you check on the net for military air operations and ground support. Whats done during airfield ops is pretty much the same except for the military specific stuff.
 
J

joshua_sx1

#3
I’ve tried your suggestion, and I haven’t found any website explaining and detailing more about this ISAGO except from the marketing side of IATA website… :notme:

…anyway, I guess it would be hard as of this time, since it is barely new audit system – (introduced only last year and they started only the audit process last March 2008)…

(…but at least “elsmar” forum perhaps, the first forum to open a discussion regarding this system…) :rolleyes:

…thanks Randy, btw… :agree1:
 
J

joshua_sx1

#4
:read: Just to give an update on this… (in case there would be someone interested)

...I guess, there is no necessity of creating an ISAGO standard manual if those sections were already covered by the organization’s existing manuals & procedures (i.e. H&S manual / procedures, Maintenance Organization Exposition, etc.)...

…you need only to create a cross-reference matrix to show which manual and/or procedures covers the required sections of ISAGO…
 
M

mimibella

#5
Hello Everybody!!!!!!!

I m working on ISAGO.IF anyone has information or a sample .please let me know specially about PAX HANDLING>

:biglaugh:Thanks
 
K

khtita

#6
ISAGO is an IATA new standard for ground service providers indépendant or affiliated to an airliner with independant HQ. IATA took from ISO, OACI,AHM..and best practices and issued ISAGO.
ISAGO is now mostly needed to improve ground operations,to reduce ground incidents, ground support equipements........and to reduce the redundancy of audits.
ISAGO is composed now of 8 esections,de-icing and fuelling are coming soon.you can download from IATA site the GOSM where all the GOSARPs are explained.
:bigwave:
 
K

khtita

#7
hello
start first with OMS: the corporate manuel,the ERP and the training manuel,the GSE...

GOOD LUCK
________________________________________________________________________
if there is no solution..............there is no problem
 
K

khtita

#9
Section 4.PAX
1. Passenger Handling Operations

1.1. General

1.1.1. accuracy of load control process, communication between Pax handling personnel and load control.

1.1.2. current edition manuals , relevant to passenger handling process

1.1.3. gsps dgr procedure + customer airline SLA.


1.2. PASSENGER CHECK-IN PROCEDURES

1.3. DANGEROUS GOODS

1.4. Security

1.5. carriage of weapons

1.6. special categgory passengers

1.7. company mail

1.8. aircraft access

1.9. passenger boarding equipment

to be continued...............................
 
F

Fridtjof Hodnebo

#10
Hi all,

My name is Fridtjof Hødnebø. I am student and as a part of a project I am working on I am to analyze the Ground Handling industry's reception of the ISAGO program. If you wish to share your opinion on the matter please visit the following thread here on elsmar:
ISAGO - the industry's perception of IATA's safety audit initiative

I cannot post links here, sorry.


Thanks a lot,
Fridtjof Hødnebø
 
Thread starter Similar threads Forum Replies Date
F ISAGO - the industry's perception of IATA's safety audit intiative Other ISO and International Standards and European Regulations 2
A Canadian Safety Labels for medical electrical equipment Canada Medical Device Regulations 0
A Applicability of Photobiological Safety Evaluation for LED used in medical devices Reliability Analysis - Predictions, Testing and Standards 1
A Should I take an online course for a career in Occupational Health and Safety? Career and Occupation Discussions 2
E 60601-1 - Tilt testing - Tensile safety factor IEC 60601 - Medical Electrical Equipment Safety Standards Series 1
Marc ISO 26262- Road vehicles – Functional safety ISO 26262 - Road vehicles – Functional safety 0
A Defining a lower ESD test level in IEC 60601 safety test IEC 60601 - Medical Electrical Equipment Safety Standards Series 5
D Safety data sheets software REACH and RoHS Conversations 2
M ECG lead leakage currents - How to specify ECG leads during electrical safety testing IEC 60601 - Medical Electrical Equipment Safety Standards Series 5
R Quality System Functional Safety Checklist / Guidance IATF 16949 - Automotive Quality Systems Standard 0
N German National Requirements - Safety Officer/Authorised Rep Other Medical Device Regulations World-Wide 0
C Where to draw the line for "sufficient evidence" to verify safety/performance of a device? CE Marking (Conformité Européene) / CB Scheme 2
A IEC 62304 safety classification, External Controls and off-label use related risks IEC 62304 - Medical Device Software Life Cycle Processes 5
A Baby food manufacture - food safety requirements Food Safety - ISO 22000, HACCP (21 CFR 120) 0
dgrainger Informational EU medical device website change from 'Growth' to 'Health and Food Safety' (6/2020) Medical Device and FDA Regulations and Standards News 0
D Safety Assurance Case Report Format ISO 14971 - Medical Device Risk Management 4
B Product Safety Responsibility - Job shop such as a machine shop AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 10
K Things to learn during lockdown.... Safety-related books/articles/threads Book, Video, Blog and Web Site Reviews and Recommendations 2
JAMESH Job Safety - Lockout/Tagout and Respiratory Protocols Manufacturing and Related Processes 3
J Raw material certificates - CC - Safety products - Sheet metal stamping IATF 16949 - Automotive Quality Systems Standard 1
M Differences in post market safety reporting for Combination Product Applicants Medical Device and FDA Regulations and Standards News 1
S Should safety checks be included in the Control Plan? IATF 16949 - Automotive Quality Systems Standard 5
adir88 Information of safety can reduce risk now? ISO 14971 - Medical Device Risk Management 12
D Is there a specific location for PPE such as safety glass holders and glove dispensers should be mounted Occupational Health & Safety Management Standards 10
M Do you need an Applicable general safety and performance requirements Checklist? EU Medical Device Regulations 2
S VW Supplier Product Safety Representative (PSB) upgrade to PSCR VDA Standards - Germany's Automotive Standards 4
J FDA wants electrical safety testing on battery powered medical device US Food and Drug Administration (FDA) 11
T Confirming The Local Safety Regulations for Equipment - I'm in Malaysia General Measurement Device and Calibration Topics 1
MrTetris Unacceptable risk and information for safety ISO 14971 - Medical Device Risk Management 16
A Contraindication Safety Statement in website - Radiotherapy equipment Other Medical Device and Orthopedic Related Topics 1
L External power supplies: How close does the safety report have to match the end-use application? IEC 60601 - Medical Electrical Equipment Safety Standards Series 4
C Safety lettering on a product CE Marking (Conformité Européene) / CB Scheme 5
M EU – Chemical Safety Report – CSR – REACH Authorisation decisions – Triton X-100 – Ortho-clinical-Use1 REACH and RoHS Conversations 0
M Informational EU – Minutes of the 24 July 2019 SCHEER Working Group on safety of breast implants in relation to anaplastic large cell lymphoma (BIA-ALCL) meeting Medical Device and FDA Regulations and Standards News 0
M EMC Directive and product safety standards CE Marking (Conformité Européene) / CB Scheme 1
S Safety Class A with no test? IEC 62304 - Medical Device Software Life Cycle Processes 1
M Informational MDCG 2019-9 Summary of safety and clinical performance A guide for manufacturers and notified bodies – August 2019 Medical Device and FDA Regulations and Standards News 0
D Requirement of Pharmacovigilance (Drug Safety) Risk Based Strategic and Tactical Audit Plan General Auditing Discussions 0
M Informational Several US FDA draft guidances, including some specific device guidances for the Safety and Performance Based Pathway Medical Device and FDA Regulations and Standards News 0
M Informational USFDA final guidance – Safety and Performance Based Pathway Medical Device and FDA Regulations and Standards News 0
M Informational Medical Device Safety Action Plan: Protecting Patients, Promoting Public Health Medical Device and FDA Regulations and Standards News 0
S System safety assesment Federal Aviation Administration (FAA) Standards and Requirements 0
M Informational TGA Consultation: Proposed changes to medical device essential principles for safety and performance Medical Device and FDA Regulations and Standards News 0
rezayatmand IEC 60601-2-18 Medical electrical equipment - Part 2-18: Particular requirements for the basic safety and essential performance of endoscopic equipmen IEC 60601 - Medical Electrical Equipment Safety Standards Series 2
B Evaluation of Basic Safety during EMC Immunity or Climate Testing IEC 60601 - Medical Electrical Equipment Safety Standards Series 0
P Is there a counterpart to the General Safety and Performance Regulations for the USA? Other US Medical Device Regulations 2
M Informational The US FDA is Recommending Transition to Duodenoscopes with Innovative Designs to Enhance Safety: FDA Safety Communication Medical Device and FDA Regulations and Standards News 0
D Summary of safety and clinical performance in GSPR MDR EU Medical Device Regulations 2
A ISO/TS 22163 Item 5.2.4 Safety policy - Example wanted Other ISO and International Standards and European Regulations 2
M Informational US FDA draft guidance – Testing and Labeling Medical Devices for Safety in the Magnetic Resonance (MR) Environment Medical Device and FDA Regulations and Standards News 0

Similar threads

Top Bottom