SBS - The best value in QMS software

Interesting Discussion Using a Wiki to implement a Quality Management System (QMS)

M

machrk

#41
Pancho

thanks for your candour - I too find there are some who are enthused - but many who feel they should only publish to a wiki if it their content is perfect without errors

I ran a wiki session at our Sharepoint Interest group last week- see attached document - please don't get hung up on my comments about wikis & controlled documents - basically I am distinguishing :agree1:wiki's purpose designed for standard procedures, manuals etc and others not in this category

cheers

@KerrieAnne & @SteelyQueen on Twitter


Hi, Shane,

Yes, that was a bit of a hurdle for us too. We overcame it with the following:

1)
Got a small group enthused about the wiki first. Our first wiki application wasn't the management system, but project to-do lists. This involved less users and they were a bit more of early-adopters.

2)
Training. We had a couple of sessions of hands-on training for every employee.

3)
Network effects. Once the wiki got past a critical mass, its benefits became so strong that (almost) everyone wants to use it.

Despite the above, there will always be some folks that do not contribute all they could or should. Any new tool provides an excellent excuse for that. Just yesterday I read something quite appropriate: "Wikis show not only how much internal experts know, but how eager they are to share their knowledge." [source].

Our wiki engine supports both WYSIWIG and wiki markup, and our users' preferences are divided about equally.
 

Attachments

Elsmar Forum Sponsor

Pancho

wikineer
Super Moderator
#42
I too find there are some who are enthused - but many who feel they should only publish to a wiki if it their content is perfect without errors
Indeed. Many a document that would be useful to an organization may never be released because it is too hard to get it right. It takes a while, but eventually folks realize that once on the wiki the documentation improves because collaboration is enabled.

please don't get hung up on my comments about wikis & controlled documents
What you say is true: "wiki is not a standard procedure...unless these were intended to be in a wiki intended for this purpose". Yet, what makes the wiki (or any other tool) fit to be a controlled document home is not the tool itelf, but a proper procedure for document control.
 
M

Migre

#46
Congratulations Pancho. Such recognition certainly lends some weight to the arguement that Wiki-based QMS's are a viable option these days. Good luck on April 20th. :applause:
 

Pancho

wikineer
Super Moderator
#48
Thank you all for the congratulations. We are of course thrilled to be a finalist. The whole company is vested on and very proud of our wiki/QMS.
 
S

sharney

#50
Hey folks, have a moronic question.
Been asked to update our Quality Manual from stone to paper.
And follow the guidlines of ISO 9001-2008.
The moronic question, "do i need to puchase these?"
:thanks:
 
Thread starter Similar threads Forum Replies Date
C Document Control using Wiki - Cannot Create all Documents as Wiki Pages Document Control Systems, Procedures, Forms and Templates 10
Pancho Using a wiki for Document Control The Reading Room 10
J Incoming Inspection Records using Excel File ISO 13485:2016 - Medical Device Quality Management Systems 2
J Using ring gauges General Measurement Device and Calibration Topics 2
M Load Cell Calibration using a totalizer on a flow meter General Measurement Device and Calibration Topics 0
P Can Neoprene be Cleaned Using Isopropyl Alcohol (IPA) Manufacturing and Related Processes 4
GreatNate Anyone using the Intellect QMS software? Quality Assurance and Compliance Software Tools and Solutions 1
chris1price Sterilization using beta radiation Other Medical Device Related Standards 2
M Using the phrase "herein referred to" Document Control Systems, Procedures, Forms and Templates 8
B Struggling with using the 5.6 version Ford Capacity Analysis Report APQP and PPAP 5
cnbrosa Study Type 1 on a CMM using a measuring support Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 4
rerusk1 MRB (Material Review Board) Process using MS Sharepoint or MS Teams Manufacturing and Related Processes 2
K 510k FDA review, will they accept Biocompatibility result generated using feasibility product lots? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 8
B AS9100D 7.1.5.2 Calibration or Verification Method using outside cal lab AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 1
U Medical Device CE Marking - Using a disposable bearing CE Marking (Conformité Européene) / CB Scheme 3
D Calibration tolerance question using Pipettes Medical Device and FDA Regulations and Standards News 1
D Risk Analysis using Monte Carlo Simulation instead of Scoring and Heat Map Risk Management Principles and Generic Guidelines 2
W Using tailoring guidelines to tailor a QMS procedure ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
Y We found out we have been using a equipment without validation for past 4 years Quality Manager and Management Related Issues 6
D Using Laboratory Notebooks in R&D and Design and Development ISO 13485:2016 - Medical Device Quality Management Systems 3
C Importer shell game - Using a third party logistics provider (3PL) in the EU EU Medical Device Regulations 5
S Work performed in Canada on US patients using US device Canada Medical Device Regulations 1
S Is using ANSI/ASQ Z1.4-2008 the correct sampling plan to determine Pass/Fail of Apparel measurements? AQL - Acceptable Quality Level 4
A What are the pros and cons of using an audit software for internal auditing? General Auditing Discussions 7
Tagin Evaluating nonconformances for escalation using Bayesian methods? Statistical Analysis Tools, Techniques and SPC 2
D Using non-conforming components even though the final assembly is conforming? Manufacturing and Related Processes 5
B Using Unreleased Documents & Process Maps for Internal Audit purposes ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 12
R Clause 7.7 Replicate, Recalibration and Intermediate checks using Artifact ISO 17025 related Discussions 1
Stoic Are any medical device companies using the 2011 FDA process validation guidance instead of GHTF/SG3/N99-10:2004? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
B Unit of Use DI (Device Identifier) - Products using the same device US Food and Drug Administration (FDA) 0
A Using Arduino based sensors for Poke-Yoke Manufacturing and Related Processes 6
M Using your Manufacturer's ISO certification ISO 13485:2016 - Medical Device Quality Management Systems 5
Ed Panek Adverse Event Clinical Trial using a 510K approved Device Other US Medical Device Regulations 6
B Using non CE parts in a machine CE Marking (Conformité Européene) / CB Scheme 1
G Gauge R&R on multiple dimensions using 3D measurement system Capability, Accuracy and Stability - Processes, Machines, etc. 6
A Hospital IT expectations for connected medical device using WIFI Medical Information Technology, Medical Software and Health Informatics 0
Proud Liberal Cp / Cpk on position using multiple MMC bonuses Capability, Accuracy and Stability - Processes, Machines, etc. 2
B Using external FDA and ISO 13485 audit as internal audit Internal Auditing 6
D Using "Particle Size Standard" templates as gauges - How to avoid giving a gauge # while using for process control? General Measurement Device and Calibration Topics 2
J Class 1 Medical Device - Using a UPC over the UDI? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 0
I Reducing CE marking cost using manufacturer test reports CE Marking (Conformité Européene) / CB Scheme 5
CPhelan Using clinical trial safety data for evidence for CE marking EU Medical Device Regulations 8
M Accredited Calibration Sevice Provider using computerized system to issue calibration certificate Qualification and Validation (including 21 CFR Part 11) 3
M Accredited Calibration Sevice Provider using computerized system to issue calibration certificate General Measurement Device and Calibration Topics 2
M Raw stock material testing discrepancy using an XRF (x-ray fluorescence) analyzer Manufacturing and Related Processes 7
Z Using FMEA for Knowledge Management FMEA and Control Plans 6
Sidney Vianna NASA to Develop a Novel Approach for All-Electric Aircraft Using Cryogenic Liquid Hydrogen as Energy Storage World News 2
S How many of you are using Robotic process automation for calibration lab management? ISO 17025 related Discussions 0
J Including Repeats in DoE using Minitab Using Minitab Software 5
S Legal Manufacturer FDA Reporting Obligations for Using New Contract Sterilization Site Other Medical Device Regulations World-Wide 0

Similar threads

Top Bottom