Audit Program

M

mcb8611

#1
#1
I have a new project that I want to start but giving all the facts, it seems that I will be finding a needle in a haystack. Does anyone know a website in the Internet that has useful audit programs. The only one I know is the knowledgespace.com by AA. Please help.

Thanks!

[This message has been edited by mcb8611 (edited 20 February 2001).]
 
Highly Rated Gage Tracking - Learn More
Elsmar Forum Sponsor
E

energy

#2
#2
Harrington Group has a program called Audit Master. You can ask for a free trial CD and use it for 30 days for evaluation. Try www.harrington-group.com. I'm not selling it but you have user rights for a 30 days free. After that, it doesn't allow you to edit.I have tried a few of their programs and purchased their CA-5. Love it.
 
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
T Robust internal audit program AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
G Organizing internal audit program for an Integrated QHSE Management System Internal Auditing 13
M What are the basics of Medical Device Single Audit Program (MDSAP)? ISO 13485:2016 - Medical Device Quality Management Systems 7
N ISO 19011:2018 - 5.4.2 "...audit program should engage in appropriate continual development..." Training - Internal, External, Online and Distance Learning 4
V IATF 16949 9.2.2.1 Internal Audit Program - "Process Changes" IATF 16949 - Automotive Quality Systems Standard 11
R Critical suppliers (Definition of) and MDSAP (Medical Device Single Audit Program) ISO 13485:2016 - Medical Device Quality Management Systems 22
M Medical Device News Health Canada - Medical Device Single Audit Program (MDSAP) Transition Plan Canada Medical Device Regulations 2
L Need HELP with Internal Audit Program ISO 13485.2003 Quality Management System (QMS) Manuals 3
S Internal Audit Program under MDSAP and 13485:2016 ISO 13485:2016 - Medical Device Quality Management Systems 10
Edward Reesor MDSAP (Medical Device Single Audit Program) Costs Canada Medical Device Regulations 7
B IATF 16949 Cl. 9.2.2.1 - Internal audit program - Types of evidence Internal Auditing 1
A MDSAP Internal Audit Program example wanted Internal Auditing 3
Ronen E FDA encourages industry to participate in Medical Device Single Audit Program (MDSAP) Other US Medical Device Regulations 10
Marc Creating an Internal Audit Program That Works for Your Organization Internal Auditing 0
Q Internal Program audit Scope for NPI 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
somashekar MDSAP (Medical Device Single Audit Program) Pilot: Please share your feedback ISO 13485:2016 - Medical Device Quality Management Systems 35
M US FDA "Single Audit Program" and Brazil Other Medical Device Regulations World-Wide 3
M ISO 13485 Certification - Internal Audit Program Required ISO 13485:2016 - Medical Device Quality Management Systems 12
Ajit Basrur IMDRF inviting comments on Audit Program and UDI ASQ, ANAB, UKAS, IAF, IRCA, Exemplar Global and Related Organizations 0
C Audit of the Corporate Audit Program 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
N LPA (Layered Process Audit) Program - Visual Shop Display Process Audits and Layered Process Audits 4
U Customer Audit Nonconformity on Internal Audit Program done by Corporate QA General Auditing Discussions 19
G FDA Voluntary Audit Report Submission Pilot Program now a final guidance document 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 6
C Aircraft Certification System Evaluation Program (ACSEP) Audit - Who can trigger it? Federal Aviation Administration (FAA) Standards and Requirements 1
RoxaneB Risk-Based Audit Results - Audit Program for Multiple Locations General Auditing Discussions 8
G What is an "Audit Program (Programme)"? General Auditing Discussions 18
Q Internal Audit Program for ISO TS 16949 IATF 16949 - Automotive Quality Systems Standard 15
Le Chiffre ISO 13485:2003 Voluntary Audit Report Submission Program ISO 13485:2016 - Medical Device Quality Management Systems 3
6 Vehicle Accident Investigation Program - Integrated compliance audit Occupational Health & Safety Management Standards 9
S Ideas for an Ideal Internal Audit Program Internal Auditing 16
S Elements of a Robust Internal Audit Program Internal Auditing 6
M Can I Stop the Internal Audit Program? Internal Auditing 21
K Military Program - Physical configuration Audit (PCA) AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 8
A DMAIC as a model for managing an Internal Audit program Internal Auditing 29
F Software Program for tracking internal audit results needed Quality Assurance and Compliance Software Tools and Solutions 2
C Changing Internal Audit Program - Regional Manager Online Audits Internal Auditing 2
E Audit Program and CAPA (Corrective Action - Preventive Action) Effectiveness ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4
D Heading an Internal Audit Program - What training is required? Internal Auditing 2
S Is MDSAP Audit Required? ISO 13485:2016 - Medical Device Quality Management Systems 2
J Average number of Nonconformances during internal quality audit for Medical Device Manufacturers Internal Auditing 3
Q AS9100:D Counterfeit internal audit questions AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
D ISO 9001:2015 Internal Audit Check Sheet ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
B Audit checklist for Sterilization Vendors ISO 13485:2016 - Medical Device Quality Management Systems 1
Ed Panek MDR Audit Comment EU Medical Device Regulations 9
R Simple tool to establish an audit schedule? General Auditing Discussions 10
P 9.2.2.2 & 9.2.2.3 Audit Cycle alignment required? IATF 16949 - Automotive Quality Systems Standard 1
R Disruptions that happen prior to surveillance audit ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
B Cycle Count Audit Discrepancy Supplier Quality Assurance and other Supplier Issues 1
R Audit from Customer - concerned with IP protection ISO 13485:2016 - Medical Device Quality Management Systems 4
I MDR Audit: NC per MDR Annex IX Administrative provisions 8. EU Medical Device Regulations 6

Similar threads

Top Bottom